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WHAT DOES CBD DO? CBD OIL AND ITS EFFECTS

What does CBD do? What does CBD stand for? Cannabidiol, or CBD, is a chemical compound found in the Cannabis sativa plant. Initially discovered in 1940, cannabidiol is a phytocannabinoid (the chemical compounds naturally found in Marijuana and Hemp plants). Despite this fact, CBD does not create any psychological effects, unlike the cannabinoid THC. Out of the 113 or more cannabinoids found in Cannabis plants, cannabidiol accounts for approximately 10-15% of the plants’ extract.

Clinical research has been investigating the positive health benefits of CBD, finding that CBD could be used to ease or remedy the symptoms of common health issues like anxiety, depression, acne, and heart disease. It may even stand as a natural alternative for pain and symptom relief when dealing with cancer.

It’s no wonder that CBD has swept through the American consumer market. Google trends and search data have proven that CBD is gradually becoming a household name. Everyone wants to know about CBD, from what it can do, its safeness for use, and the total extent of its effects. This article aims to answer some of these common questions while also discussing current scientific data on CBD use.

Does CBD oil make you high?

The most common misconceptions about CBD are based on the question, “Are CBD and Marijuana the same thing?”

In short, no. While CBD is an essential compound of cannabis found in both Hemp and Marijuana plants, you cannot get high from using CBD. A report by the World Health Organization states that ”in humans, CBD exhibits no effects indicative of any abuse or dependence potential…to date, there is no evidence of public health-related problems associated with the use of pure CBD.”

What part of cannabis does make you get high?

The psychological effects are colloquially known as “getting high” come from another cannabinoid called THC. The THC attaches to cannabinoid receptors in the brain, which then creates the psychoactive effects most people associate with Marijuana use.

CBD vs. THC

Both compounds are part of the Cannabis plant, but high concentrations of THC are only found in Marijuana. The Hemp plant is defined as those varieties that contain less than 0.3% THC, so it cannot create a high. CBD is found in both types of Cannabis; however, the Hemp plant is used more commonly for CBD oil extraction.

Are CBD and THC legal?

In terms of legality, CBD is readily available for purchase in America thanks to the 2018 Farm Bill. The bill included a provision that federally legalized Hemp for agricultural production, so long as it contains no more than 0.3 percent THC, a level that will not do not make the user get high. This allowed the CBD-only industry to take off, and now CBD can be purchased online and in all 50 states.

Marijuana, on the other hand, is legal for sale and consumption in only a handful of states in the U.S. due to its THC content. Although THC containing materials above 0.3% are still considered a Schedule 1 controlled substance by the federal government, medical Marijuana is legal in 33 states, and recreational Marijuana is legal in 11 states plus the District of Columbia.

Eight Scientific Health Benefits CBD Oil

As noted, studies on CBD have proven it can provide relief from many different ailments and symptoms. CBD has also been touted as a supplement for other general health and wellness issues. Despite CBD being somewhat controversial or misunderstood, it is imperative to understand that CBD is considered safe for human use, as it contains zero addictive properties or elements that get you high, such as the THC compound found in Marijuana.

Thus far, scientific research on CBD has demonstrated it has the potential to provide the following benefits to its users:

1. Relieves chronic pain and inflammation

CBD may offer an alternative to moderating some types of chronic pain. Many people who have fibromyalgia have affirmed that they felt relief after using cannabidiol oil. Further studies have proven mechanisms by which cannabidiol oils inhibit inflammatory and neurotic pain. Using an animal model, a study from the European Journal of Pain demonstrated that CBD oil, when applied to the skin, could help lower pain and inflammation as a result of arthritis.

More research is needed to confirm these benefits for humans further. However, many CBD oil users claim that it does reduce pain and inflammation caused by various chronic health conditions.

2. Calms or stops epilepsy

Videos showing the beneficial effects of CBD on children with epilepsy are found all over the internet. Many studies have shown that cannabidiol possesses anti-seizure properties that can effectively treat children with drug-resistant forms of epilepsy. A study published in the New England Journal of Medicine revealed that CBD use reduced the occurrence of seizures by 23 percent over those taking a placebo.

New research has explored using CBD to treat some of the cruelest childhood epilepsy syndromes, such as Dravet syndrome and Lennox-Gastaut syndrome (LGS). Typically, these syndromes do not respond to anti-seizure medicines. However, in many of the research cases, cannabidiol oil decreased the number of seizures the patient suffered and eliminated seizures in others.

In June 2018, the FDA approved Epidiolex, the first cannabis-derived medicine containing cannabidiol, to treat these severe conditions. Epidiolex also happens to be the first FDA-approved drug that contains a purified form of a Marijuana extract. The drug mitigates the seizures and sometimes gets rid of them entirely. Panacea Life Sciences manufactures a similar version of this product since it is naturally produced from the Hemp plant.

3. Reduces oxidative stress

Oxidative stress is caused when the body has an excess of free radicals, which are molecules that contain an uneven number of electrons as well as oxygen. In periods of oxidative stress, the body’s antioxidants are unable to neutralize all the free radicals. This health issue is relatively new due to increased environmental toxicity around the world.

4. Regulates blood pressure

Heart disease is one of the top causes of death in the United States. High blood pressure can cause hypertensive heart disease because it affects how the heart’s arteries and muscles work. High blood pressure increases the amount of work the heart has to do to pump blood throughout the body, which can lead to the heart becoming enlarged. Oftentimes hypertension is associated with an increased risk for stroke and kidney disease. A 2017 study published in JCI Insight revealed that CBD could help regulate blood pressure fluctuations engendered by stress. Thus, CBD may be used as a preventative measure for heart health.

5. Fights multi-resistant bacteria

CBD has the unconventional means to fight certain kinds of bacteria, typically the drug-resistant strains. In one study, CBD was found to be bactericidal against strains of staphylococci and streptococci. A 2011 study showed that cannabidiol could reduce the tuberculosis progression found in rats; however, the study found that this may be because of slowed the increase of T cells. More research is required to better understand cannabidiol’s role in fighting infections.

6. Treats symptoms of Type 1 diabetes

Type 1 diabetes occurs when the body’s immune system attacks the pancreatic cells that produce insulin, which then causes inflammation. Research by Clinical Hemorheology and Microcirculation in 2016 showed that cannabidiol could ease pancreatic inflammation and lowered the occurrences of Type 1 diabetes in mice.

7. Alleviates skin conditions

Numerous studies have proven that CBD can clear up skin issues like eczema by encouraging unconventional cell death. CBD can also regulate excess sebum (oil) production, which helps to prevent acne. Coupled with its anti-inflammatory properties, CBD can be an effective anti-oxidant in skin care, much like vitamins C or E.

8. May slow progression of Alzheimer’s disease

The Journal of Alzheimer’s Disease published a study in 2014, showing CBD can slow the growth of social recognition memory deficit in people in the early stages of Alzheimer’s. This means CBD may help improve their sense of recognizing familiar faces. It is also an effective way to make the symptoms of the disease less intense.

Is CBD oil safe?

CBD oil, to a large extent, has been shown to treat symptoms of many different ailments and is generally regarded as safe (GRAS) for human use. Adverse side effects of CBD are mild and rare, largely depending on dosage levels and the individual user. The side effects may include nausea, fatigue, and irritability. Cannabidiol can also raise levels of coumadin, a blood thinner, or impact levels of other medications in the blood.

However, as demonstrated above, scientific research has shown that cannabidiol helps treat specific ailments and provides relief for other everyday conditions and irritations.

Takeaway

It’s clear from the research on CBD that it interacts positively with the body. CBD oil can provide relief for specific conditions and symptoms while also providing general health and wellness benefits to its users. If you’re considering trying the supplement and you’re on other medication, be sure to consult with your doctor for proper guidance.

References:
Ministry Of Hemp
Drug Abuse
FDA
Health Line
Insight
Springer Link
NCBI
NCBI
NCBI

Panacea Life Sciences Holdings, Inc. Celebrates National CBD Day (August 8th) By Shifting To An “Everyday Low Pricing Model” To Meet Customer Needs

The new pricing model for Panacea’s natural health & wellness products will not only help customers afford natural remedies in this strained economy but will provide consistency and a promise that is better aligned with the company’s vision to help people and pets live their best lives, naturally.

Golden, Colorado,August 8, 2023/PRNewswire/ — Panacea Life Sciences Holdings, Inc.

(OTCQB:PLSH) (“Panacea” or the “Company”), today announced the launch of their shift to an everyday low price pricing model for their full line of CBD products for pets and people. Panacea Life CBD products are regarded as some of the highest quality CBD products on the market due to their unique seed-to-sale approach that allows for premier quality control and opportunities to innovate distinct ingredient formulations that enhance apage1image63726112nd ensure maximum efficacy.

“Panacea has been at the forefront of delivering functional CBD products to the consumer market since 2017, yet we are still seeing an unwelcome misunderstanding at the federal, retail, and consumer levels about this amazing natural plant” stated Nick Cavarra, President of Panacea. “For many consumers, the cost of CBD products has been too expensive – particularly in this current inflationary period – so we felt it was important to bring affordability to these products that have massive potential to help people feel better every day.”

The new pricing strategy allows Panacea’s wide array of products to be more comparable to other nutraceutical and even pharmaceutical products on the market. One of the Company’s goals is to provide products that are just as effective and priced near common over-the-counter drugs like ibuprofen, aspirin or naproxen. With the growing rate of people who are more mindful and motivated to seek out clean, natural and organic products, Panacea is wise to put their specialty products on the same playing field as the typical “go-to” medicines.

Launching their pricing changes on National CBD Day, August 8th, is ideal to bring CBD to the forefront of natural health products – a move that many suspect will be well received. Along with the new pricing, Panacea is also making a notable shift toward better aligning with their company mission:

Providing Alternative Remedies for Natural Health and Wellness.

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In the coming months and beyond, Panacea is both well-equipped and committed to generating significant revenue growth in the billion-dollar nutraceutical/natural health and wellness space to provide more consumers more opportutnities to take advantage of natural, clean, non-addictive health solutions. Positive industry insights and projections prove the Company is headed in the right direction and capitalizing early on the relatively young industry’s impressive growth is sure to put Panacea on the map and provide significant value to our shareholders.

 

 

About Panacea Life Sciences Holdings, Inc.

Panacea Life Sciences Holdings, Inc. (PLSH) is a holding company structured to develop and facilitate manufacturing, research, product development and distribution in the high-growth, natural human, and animal health & wellness market segment. Its subsidiary, Panacea Life Sciences, Inc. (PLS), is a woman-founded and led company dedicated to manufacturing, distribution, research and production of the highest-quality nutraceutical, cannabinoid, mushroom, kratom and other natural, plant-based ingredients and products. PLS operates out of a 51,000 square foot, state-of-the-art, cGMP facility in Golden, Colorado. If you would like more information about how Panacea is providing alternative remedies for natural health and wellness, please visit www.panacealife.com.

Cautionary Note Regarding Forward-Looking Statements

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This press release contains forward-looking statements within the meaning of the Private Securities Litigation Reform Act of 1995, including statements. Forward-looking statements involve risks and uncertainties that could cause actual results to differ materially from those projected or anticipated. These risks and uncertainties include, but are not limited to, risks arising from our ability to obtain raw materials and ingredients from our vendors, our ability to fulfill purchase orders on a timely manner, our ability to attract financing on terms and subject to conditions, acceptable to us, our ability to operate profitably and continue as a going concern, effects of Covid-19 on our business and the businesses of our customers and suppliers, the ability to manage an acquisition program and integrate acquisitions, as well as those risks and uncertainties described in our annual report on Form 10-K for the fiscal year ended Decembe 31, 2022 under the heading “Risk Factors”. Any forward-looking statement made by us herein speaks only as of the date on which it is made. Factors or events that could cause our actual results to differ may emerge from time to time, and it is not possible for us to predict all of them. We undertake no obligation to publicly update any forward-looking statement, whether as a result of new information, future developments, or otherwise, except as may be required by law.

Contact:

[email protected]

800-985-0515

Source: Fortune Business Insight

Panacea Life Sciences Holdings, Inc. Continues Pursuit of High Growth Health and Wellness Products with Acquisition of Sierra Sage, LLC and Halucenex from Melodial Global Health

Golden, Colorado,August 2, 2023/PRNewswire/ — Panacea Life Sciences Holdings, Inc. (OTCQB:PLSH) (“Panacea” or the “Company”), today announced it has entered into a Letter of Intent with Melodial Global Health (ASX:ME1)(formerly Creso Pharma) to acquire Sierra Sage Herbs (“Sierra”), maker of the best-selling Geen Goo, Southern Butter and Good Goo natural products and Halucenex, a company researching novel psychedelic compounds. The deal would

extend Panacea’s footprint into natural first aid and body care products, and establishes a strong tie with Melodial through a significant stock ownership stake.

Sierra Sage, which counts 90,000 points of distribution across the US including Whole Foods, Walmart, Amazon, Target.com, CVS, Walgreens, Rite Aid, Kroger, and Food Lion, among others, will continue to operate under its existing leadership while gaining access to Panacea’s 51,000 square foot manufacturing, production and distribution facility in Golden, Colorado.

Originally founded in 2008 by sisters Jodi and Jen Scott and their mother Kathy Scott, Sierra Sage has grown from a home-based, women-run start-up to a leader in the natural health products space. Its biggest line, Green Goo, is a collection of plant-based portable first aid and body care products that are crafted using a proprietary lipid-infusion process, rather than with pre-made extracts. This unique process increases the medicinal value of its salves, making its natural healing properties some of the most potent in the market. Green Goo ingredients are organic whenever possible, are sourced using fair trade principles, and include no harmful chemicals. The company also offers a line of hemp-infused health products through its Good Goo brand and a line of intimate skin care products through its recently launched Southern Butter brand.

“My family and I started Sierra Sage Herbs because we saw a real white space in the market for naturally safe, effective, simple wound care that was both portable and accessible,” said Sierra Sage Herbs CEO and co-founder, Jodi Scott. “We are thrilled to be joining with another woman founded Colorado-based company that shares our ideology to pursue ESG (Environmental, Social, Governance) goals in health, science and wellness.”

Halucenex is a life sciences development company with a focus on researching novel psychedelic compounds, including developing and licensing psychedelic compounds for pharmaceutical and nutraceutical markets, and conducting clinical trials on the medical benefits of psychedelic medicine. Halucenex operates a 6,000 sq. ft. medical facility in Windsor, Nova Scotia with 6 treatment rooms and a secure laboratory dedicated to performing psychedelic-assisted psychotherapy and clinical research. Halucenex intends to maintain control over all aspects of the product development process – mycological research, extraction technology, and synthetic formulation as well as drug delivery technologies, psychedelic-assisted psychotherapy and regulatory affairs.

Sierra Sage and Halucenex will join the enterprise group at Panacea that includes health and wellness including Panacea branded CBD/CBG and nutraceuitical production in Golden Colorado. Other planned acquisitions in the Panacea portfolio include N7, a chain of Kratom and Kava bar

locations in South Florida which was signed in July and expected to be completed in the second half of 2023.

Panacea intends to position itself to provide a comprehensive menu of natural and organic health and wellness products catering to all segments of the health and wellness minded community, while supporting research into important medical and health challenges, such as the effects of CBD/CBG/psilocybin on conditions such as irritable bowel syndrome, pain management, brain injury and PTSD.

“Adding Sierra Sage and Halucenex to the family helps Panacea achieve its goals of generating revenues from numerous naturally found products and ingredients” said Leslie Buttorff, CEO of Panacea. “Melodial’s decision to focus on its main products while collaborating with us to expand into the US market should well-position our group for unbridled success as an industry leader. It is a vote of confidence by an established cannabis company in support of our efforts. Halucenex fits well into our new health and wellness focus as we have spent the last six months developing new mushroom related products. We hope to capture significant market share in the three categories of mushroom products under development — functional, amanita and psilocybin — while enhancing our on-going research efforts at Colorado State University at the Panacea Cannabinoid Lab in order to produce valuable information about these emerging compounds.”

The purchase price for the acquisition will be based upon 1X trailing 12 months audited sales of Sierra Sage, with a projected $2.0 million of the purchase price payable in cash and the balance in restricted common stock. Melodial will be subject to restrictions on transfer of such shares and a lockup for a two year period.

Closing of the acquisition is subject to satisfaction of customary terms and conditions for a

transaction of this kind, including completion of due diligence, negotiation of definitive documents, approval of the boards of directors of Melodial and Panacea, availability of financing for the cash portion of the purchase price and losses from operations following acquisition, on terms, and subject to conditions, acceptable to Panacea in its sole discretion, and the availability of audited financial statements for the prior two completed fiscal years for Sierra Sage and Melodial.

About Panacea Life Sciences Holdings, Inc.

Panacea Life Sciences Holdings, Inc. (PLSH) is holding company structured to develop and facilitate manufacturing, research, product development and distribution in the high-growth,

natural human and animal health & wellness market segment. Its subsidiary, Panacea Life Sciences, Inc. (PLS) is a woman-founded and led company dedicated to manufacturing, distribution, research and production of the highest-quality nutraceutical, cannabinoid, mushroom, kratom and other natural, plant-based ingredients and products. PLS operates out of a 51,000 square foot, state-of-the-art, cGMP facility in Golden, Colorado. If you would like more information, please visit www.panacealife.com

About Sierra Sage Herbs

Committed to making the best all-natural, plant-based skin care products, Sierra Sage Herbs, now part of Creso Pharma, is on a mission to spread goodness, empower change and redefine natural body care. Founded in 2008 by sisters Jodi and Jen Scott and their mother Kathy Scott, the company’s natural products brands include the wildly popular Green Goo and Southern Butter, which are sold across more than 90,000 points of distribution around the US. A certified “B Corp.”, Sierra Sage aligns and partners with charities, aid organizations, and causes both in the

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United States and around the world. To learn more please visit: www.sierrasageherbs.com.

Cautionary Note Regarding Forward-Looking Statements

This press release contains forward-looking statements within the meaning of the Private Securities Litigation Reform Act of 1995, including statements. Forward-looking statements involve risks and uncertainties that could cause actual results to differ materially from those projected or anticipated. These risks and uncertainties include, but are not limited to, risks arising from our ability to obtain raw materials and ingredients from our vendors, our ability to fulfill purchase orders on a timely manner, our ability to attract financing on terms and subject to conditions, acceptable to us, our ability to operate profitably and continue as a going concern, effects of Covid-19 on our business and the businesses of our customers and suppliers, the ability to manage an acquisition program and integrate acquisitions, as well as those risks and uncertainties described in our annual report on Form 10-K for the fiscal year ended December 31, 2022 under the heading “Risk Factors”. Any forward-looking statement made by us herein speaks only as of the date on which it is made. Factors or events that could cause our actual results to differ may emerge from time to time, and it is not possible for us to predict all of them. We undertake no obligation to publicly update any forward-looking statement, whether as a result of new information, future developments, or otherwise, except as may be required by law.

Contact:

[email protected]

800-985-0515

Melodiol to streamline portfolio with Up To A$30m asset sale to US Listed Panacea – Maintaining significant stake in spin-off vehicle

Highlights:

  • Melodiol secures a non-binding LOI with Panacea Life Sciences Holdings, Inc. (‘Panacea’) (OTCQB: PLSH), a US company specialising in manufacturing, R&D, and distribution of high-quality, GMP-certified health & wellness products, for the sale of Sierra Sages Herbs, LLC (‘SSH’) and Halucenex Life Sciences Inc. (“Halucenex”) for an initial approximate US$5m in cash and scrip
  • LOI includes additional earn-out components valued at up to US$15m, which will allow Melodiol to further increase its shareholding in Panacea should conditions be met following SSH’s potential revenue growth
  • Panacea’s recent operational progress includes acquisitions of eight retail locations offering VAPE and CBD products in Tampa, Florida, generating US$2.9m of annual revenues for the fiscal year ended 31 Dec 2022, and a research collaboration with Colorado State University’s Cannabinoid Research Centre (CRC)
  • Panacea, through its diverse trademark portfolio (PANA Health, PANA Beauty, PANA Sport, PANA Pet, & PANA Life), operates across the entire cannabinoid value chain and achieved significant customer growth during Q1 CY2023
  • Panacea is headquartered in Golden, Colorado where it operates a sophisticated 51,000 square foot, cGMP-certified facility
  • Melodiol’s divestment of SSH and Halucenex allows for concentration on group profitability, via the substantial growth at Health House International and Mernova Medicinal Inc., with the purchase price including US$2m in cash and the balance in Panacea common stock, promising further upside potential
  • Post-transaction, Melodiol will be the largest shareholder in Panacea, enabling a strategic expansion into the US market. This aligns with the Company’s long stated objective to increase exposure to US capital markets
  • Panacea’s expertise will aid in the growth of SSH and Halucenex, significantly reducing Melodiol’s cash burn, and allowing ME1 to focus on accelerating the group’s near term profitability
  • Transaction enables Panacea, a complementary US specialist business, to collaborate with SSH and Halucenex, driving growth and pursue cash flow positivity for SSH via potential synergies. Additionally, if completed, it would secure continued funding for Halucenex’s progression into successful Phase II and forthcoming Phase III trials. This strategic move would also significantly decrease Melodiol’s cash burn
  • Consideration of A$30m highlights management’s view of Melodiol’s operating subsidiary value – further value accretive transactions for shareholders are also being explored
  •  

    Strategic Rationale:

    Melodiol’s Letter of Intent (LOI) to sell its earlier stage business units, SSH and Halucenex, into the specialised US-based CBD firm, Panacea, is a strategic leap towards financial agility. This move decisively decreases cash outflows for Melodiol while leveraging Panacea’s capacity to drive growth. This decision emphatically reaffirms Melodiol’s direction and rationale to escalate sales and expedite profitability, as mirrored in CY2023 sales to date of $8.6m nearing the previous year’s record revenues of $8.7m.

    In synergy with Panacea, Melodiol is poised to unlock value from early-stage SSH and Halucenex, thereby strengthening its balance sheet and accelerating an overall cash-flow positive portfolio. Moreover, the divestment reduces significant operating expenditure and capital expenditure for ME1, facilitating significant cost savings as Panacea’s highly skilled team accelerate the growth of SSH and Halucenex. Post-transaction, Melodiol’s substantial stake in Panacea offers potential upside linked to SSH and Halucenex’s operational progress and a non- dilutive funding source for scaling international operations. Crucially, this move amplifies Melodiol’s visibility in the North American market, congruent with its ambition for a NASDAQ listing.

    Melodiol Global Health Limited (ASX:ME1, FRA:1X8) (‘Melodiol’ or ‘the Company’), is delighted to announce a non-binding Letter of Intent (LOI) with the US-based entity, Panacea Life Sciences Holdings, Inc. (‘Panacea’) (OTCQB: PLSH). The LOI pertains to the divestment of two of Melodiol’s prominent business units, Sierra Sage Herbs, LLC (“SSH”) and Halucenex Life Sciences Inc. (“Halucenex”), for an up-front aggregate consideration of approximately U$5m in cash and scrip. The LOI also includes an additional US$15m in earn-out clauses, which if met, will provide additional value to Melodiol.

    Panacea Life Sciences Holdings (https://panacealife.com/), is an OTCQB-listed holding company specialising in the development, manufacturing, research, and distribution of GMP-certified health & wellness and pet care products, chiefly those originating from hemp and CBD.

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    Its subsidiary, Panacea Life Sciences, Inc., driven by strong female leadership, prides itself on the research, production, and distribution of the highest-quality nutraceutical, cannabinoid, mushroom, kratom, and other natural, plant-based products. Panacea operates from a sophisticated 51,000 square foot, cGMP- certified facility in Golden, Colorado, ensuring unparalleled quality standards.

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    The proposed divestment of SSH and Halucenex will not only furnish Melodiol with non-dilutive funding but also a strategic shareholding in Panacea. This creates an avenue for potential upside exposure to Panacea’s thriving US health products business.

    This agreement marks the initial phase of Melodiol’s strategic plan to unlock intrinsic portfolio value, extend its footprint in the US markets, and underline the superiority of its assets. The proposed transaction serves as an affirmation of Melodiol’s ability to divest itself of specific assets, thereby propelling growth and expediting the unlocking of shareholder value.

    Management commentary:

    Chief Executive Officer Mr William Lay said: “We are pleased to announce this Letter of Intent, which sets out the proposed terms of the potential transaction that would add significant value for both Melodiol and Panacea.

    “The provisional consideration terms reflect the significant upside potential of SSH and Halucenex, and the deal has been structured to allow both counterparties to leverage their respective strengths while sharing in the opportunity for future growth.

    “For Melodiol, the proposed transaction also provides the Company with a material non-dilutive cash consideration at an important juncture in its growth phase. It follows a consistent period of record revenue growth across our continuing operations, and presents the group with a strong strategic rationale to complete the transaction and deploy resources in pursuit of ongoing growth in top-line revenues and cash flow.”

    About Panacea

    Panacea has made strong operational progress recently, which provides Melodiol with confidence in the group’s ability to drive growth through SSH and Halucenex. This includes an ongoing research collaboration with Colorado State University’s Cannabinoid Research Center (CRC) to solve important industry issues and to better understand how cannabinoids work in the body, 100% increases in its contract manufacturing customer growth during Q1 CY2023, exclusive distribution agreements targeting the UK market and retail agreements with US retail groups.

    Panacea through its portfolio of trademarks, IP suite, and registrations (PANA HealthTM, PANA Beauty, PANA Sport, PANA Pet, & PANA Life) is able to operate in every segment of the cannabinoid product value chain. Due to Panacea’s products containing little to no THC, their products are able to be sold across the US and internationally, through a multi-faceted sales strategy tailored to the growing demand for alternative life science therapies. This strategy includes:

    • Global E-Commerce platform for fulfilling orders and shipping worldwide, where legally permitted.
    • Direct pharmacy placement.
    • Direct placement in retail stores, salons, spas, athletic facilities, etc.
    • Intelligent vending machines.
    • E-Commerce based systems and social media.

    The group’s recent developments highlight a number of opportunities to benefit SSH and Halucenex, while each division continues its operational trajectory.

    Transaction terms:

    Subject to due diligence being satisfied and the conditions set out below, Panacea would acquire SSH and Halucenex free and clear of all encumbrance for a purchase price totalling US$20m based upon and subject to meeting certain milestones applicable to meeting forecasted revenue associated with sales by SSH following closing of the transaction, based on the 1x the 12 month trailing audited net sales of SSH as publicly reported and is payable as follows:

    • US$2m cash payment, upon closing of the transaction. At the election of Melodiol the cash payment may be converted into common stock in Panacea (“Panacea Stock”) with a deemed issue price of the 20 day volume weighted average price (“VWAP”) from the election date prior to the closing of the transaction;
    • Estimated US$3m worth of Panacea Stock with an issue price per Panacea Stock equal to the 20 day VWAP ending on and including the closing date of the transaction; and
    • Subject to the following milestones (set out below) being met by SSH the Company will receive:

    o US$10,000,000 worth of Panacea Stock with an issue price per Panacea Stock equal to the 20 day VWAP ending on and including the date the Milestone is achieved, if during a 36 month period commencing the date after the closing date of the transaction (“Earn Out Period”) SSH’s revenues are a gross margin of at least 30% and net margin of at least 20% (“Qualified Sales”) equal or exceed US$10,000,000 per year for two consecutive fiscal years; or

    o US$10,000,000 worth of Panacea Stock with an issue price per Panacea Stock equal to the 20 day VWAP ending on and including the date the Milestone is achieved, if during the Earn Out Period the Qualified Sales are at least $15,000,000 per year in any of the first or second fiscal year; and

    o US$5,000,000 worth of Panacea Stock with an issue price per Panacea Stock equal to the 20 day VWAP ending on and including the date the Milestone is achieved, if during the Earn Out Period the Qualified Sales are at least US$20,000,000 in any fiscal year prior to expiration of the Earn Out Period.

    The cash component of the purchase price may, at the option of Melodiol, be converted into additional Shares in Panacea at the aforementioned VWAP price on the date of notice of exercise, prior to the closing date of the transaction.

    The closing of the transaction will be subject to customary conditions, including, without limitation:

    • Panacea’s satisfactory completion of due diligence of SSH and Halucenex;
    • receipt of applicable corporate approvals of the transaction by the board ofdirectors and shareholders, as applicable;
    • the execution of the definitive agreement and any ancillary agreements;
        • the receipt of any regulatory approvals and third-party consents;
        • financing (debt or equity) arrangements for Panacea’s $2m cash payment and projected cash flow deficits from the transaction, on terms satisfactory to Panacea;
        • certain key management personnel and employees entering into consultancy and restrictive covenant agreements with Panacea on terms agreed to with Panacea;
        • confirmation that SSH and Halucenex own their respective intellectual property or licenses and have all required approval for all business operations and ownership including legal and regulatory approvals, by all regulatory agencies; and
        • there being no material adverse change in the business, results of operations, prospects, condition (financial or otherwise) or assets of SSH and Halucenex.

      Sydney based, EverBlu Capital Corporate Pty Ltd acted as corporate advisor to Melodiol on the transaction and will receive a fee of 7.5% of the transaction, in line with its Corporate Advisory and Transaction Mandates which have been previously announced to the market. Steinepreis and Paganin acted as legal counsel to Melodiol.

      Paradox Capital Partners, LLC acted as advisor to Panacea.

      Next steps

      Melodiol is working closely with Panacea management to assist the group’s due diligence process. Per the LOI, both parties have agreed that until such time as the LOI is terminated Panacea has the sole and exclusive right to consider the transaction and any investment in or transaction related to SSH and Halucenex or the respective business or assets.

      The LOI will automatically terminate upon the earlier of:

    • the execution of the definitive agreement;
    • Melodiol and Panacea mutually agree to terminate the LOI; or
    • 90 days following the execution of the LOI (executed today, 2 August 2023)Due diligence remains ongoing and should this be satisfied, both parties will enter into a definitive agreement for the sale.-Ends-

      Authority and Contact Details

      This announcement has been authorised for release by the Board of Directors of Melodiol Global Health Limited.

For further information, please contact:
Investor Enquiries
Melodiol Global Health Limited
E: [email protected] P: +61 (0) 497 571 532

About Melodiol
Melodiol Global Health Limited (ASX:ME1) brings the best of cannabis and other plant- based products to better the lives of people and animals. Melodiol strives for the highest quality in its products. It develops cannabis, hemp-derived and other plant based therapeutic, nutraceutical, and lifestyle products with wide consumer reach.
To learn more please visit: https://melodiolglobalhealth.com/ Melodiol offices:
Australia: Suite 5 CPC, 145 Stirling Hwy, Nedlands, WA, 6009
Canada: 59 Payzant Drive, Windsor, Nova Scotia, B0N 2TO and 50 Ivey Ln, Windsor, Nova Scotia, B0N 2TO

Panacea Life Sciences Holdings, Inc. Chief Scientific Officer, Dr. James Baumgartner, is Featured on The Stock Day Podcast

Phoenix, Arizona–(Newsfile Corp. – July 18, 2023) – The Stock Day Podcast welcomed Panacea Life Sciences Holdings, Inc. (OTCQB: PLSH) (“the Company”), a holding company structured to develop and facilitate manufacturing, research, product development and distribution in the high-growth, natural human and animal health & wellness market segment. Chief Scientific Officer, James Baumgartner, PhD, joined Stock Day host Kevin Davis.

Davis began the interview by asking about the Company’s background and current projects. “Panacea Life Sciences is a health and wellness company,” said Dr. Baumgartner. “We started off as an industrial hemp cannabinoid company and what we’ve been doing is harnessing our manufacturing capabilities for soft gels, liquid fills, and topical lotions to make products that are going to benefit people’s everyday health,” he shared. “This ranges from cannabinoid medications and dietary supplements, as well as unique skin moisturizers.”

“Could you tell me more about your company’s expansion into the mushroom market?” asked Davis. “Functional mushrooms are extraordinarily fascinating,” said Dr. Baumgartner. “The mushroom market is divided into three segments: functional mushrooms, schedule one mushrooms, which contain psilocybin, and the Amanita Muscaria mushroom,” he explained. “We’ve been looking at each one of these spaces in terms of developing new products to help people with specific conditions or needs.”

“How do mushrooms serve as dietary supplements?” asked Davis. “One of the active compounds in mushrooms is called beta-glucan,” said Dr. Baumgartner, before elaborating on different types of mushrooms and their applications, which can include improved memory, immune function, gut health, and exercise performance and endurance.

“Could you elaborate on the Amanita Muscaria mushroom?” asked Davis. “This is the mushroom that is seen all over the place,” said Dr. Baumgartner, adding that it can be easily identified by its red color and white dots. “This mushroom has intoxicating properties,” he said, noting that the mushroom has been used historically for visions and healing properties. “The active component that produces a euphoric feeling and intoxication is called muscimol,” said Dr. Baumgartner. “At smaller doses, this is a great sleep inducer and at larger doses it will create a euphoric high.”

“We also think this compound may help to improve anxiety and could be useful for those experiencing mild forms of PTSD and depression,” continued Dr. Baumgartner. “Those are things that we are taking a look at in terms of developing things into meaningful products.”

“How is Panacea working to develop these new sources for dietary supplements?” asked Davis. “We have a collaboration with Colorado State University to develop analytical methods to measure the active components of each one of these mushroom species,” said Dr. Baumgartner, adding that this process also allows the company to identify high levels of heavy metals in the mushrooms. “By developing these methods with CSU, we can enter dietary supplement clinical trials.”

 

“The second thing that we are doing is blending different natural ingredients together to create a better product,” shared Dr. Baumgartner, adding that the Company is working with performance and endurance enhancing compounds and blending them with ingredients like ginseng to further improve athletic performance.

To close the interview, Dr. Baumgartner encouraged listeners and shareholders to keep up-to-date on the Company’s current and upcoming projects as they continue to expand their portfolio of cannabinoid and mushroom-based products in the health and wellness industry.

To hear the entire interview with Dr. James Baumgartner, follow the link to the podcast here: https://audioboom.com/posts/8336605-panacea-life-sciences-holdings-inc-chief-scientific-officer-dr-james-baumgartner-is-featured.

Investors Hangout is a proud sponsor of “Stock Day,” and Stock Day Media encourages listeners to visit the company’s message board at https://investorshangout.com/.

About Panacea Life Sciences Holdings, Inc.

Panacea Life Sciences Holdings, Inc. (OTCQB: PLSH) is a holding company structured to develop and facilitate manufacturing, research, product development and distribution in the high-growth, natural human and animal health & wellness market segment. Its subsidiary, Panacea Life Sciences, Inc. (PLS) is a woman-founded and led company dedicated to manufacturing, distribution, research and production of the highest-quality nutraceutical, cannabinoid, mushroom, kratom and other natural, plant-based ingredients and products. PLS operates out of a 51,000 square foot, state-of-the-art, cGMP facility in Golden Colorado. If you would like more information, please visit www.panacealife.com.

Cautionary Note Regarding Forward-Looking Statements

This press release contains forward-looking statements within the meaning of the Private Securities Litigation Reform Act of 1995, including statements. Forward-looking statements involve risks and uncertainties that could cause actual results to differ materially from those projected or anticipated. These risks and uncertainties include, but are not limited to, risks arising from supply chain disruptions or our ability to obtain raw materials as well as similar problems with our vendors, our ability to fulfill purchase orders on a timely manner, our ability to fully collect money for our purchase orders, the risk of customers returning our products, impact of the pandemic including new variants on our workforce, as well as those risks and uncertainties described by us in our annual report on Form 10-K for the fiscal year ended December 31, 2022 under the heading “Risk Factors.” Any forward-looking statement made by us herein speaks only as of the date on which it is made. Factors or events that could cause our actual results to differ may emerge from time to time, and it is not possible for us to predict all of them. We undertake no obligation to publicly update any forward-looking statement, whether as a result of new information, future developments, or otherwise, except as may be required by law.

Contact:
Nick Cavarra
[email protected]
800-985-0515

About The “Stock Day” Podcast

Founded in 2013, Stock Day is the fastest growing media outlet for Nano-Cap and Micro-Cap companies. It educates investors while simultaneously working with penny stock and OTC companies, providing transparency and clarification of under-valued, under-sold Micro-Cap stocks of the market. Stock Day provides companies with customized solutions to their news distribution in both national and international media outlets. The Stock Day Podcast is the number one radio show of its kind in America.

 

SOURCE:
Stock Day Media
StockDayMedia.Com
(602) 821-1102

Panacea Life Sciences Holdings, Inc. Enters Into Agreement to Natural Health and Wellness Chain of Retail Locations in Tampa, Florida

GOLDEN, Colo., July 10, 2023 (GLOBE NEWSWIRE) — Panacea Life Sciences Holdings, Inc. (OTCQB: PLSH) (“Panacea” or the “Company”), a plant-based natural health ingredient and product company, today announced it has entered into agreements to acquire eight retail locations in the Tampa, Florida area, offering Kava, Kratom, VAPE and CBD products and beverages operating as Nitro Kava & Kratom, including inventory, equipment and recipes, distribution facilities and a warehouse located in Largo, Florida, generating $2.9 million of annual revenues (unaudited) for the fiscal year ended December 31, 2022.

The purchase price for the acquisition consists of no cash and the agreement to issue approximately 85,000 shares of a new class of convertible preferred stock, which is convertible into approximately 8.5 million shares of common stock to the seller. The seller will be subject restrictions on transfer of such shares and a lockup for a two year period.

Panacea plans to operate and further develop an expanding Florida chain of natural health and wellness retail stores serving high quality plant-based products such as Kava and Kratom and plans to introduce new mushroom products and Kratom Energy drinks.

The long-term objective is for Panacea to own and or operate hundreds of stores that offer Kava Kratom, CBD, mushroom and vape products.

“We are excited to finalize the acquisition of a popular retail chain and innovative distribution business as PLSH expands its footprint into the natural plant-based market segment. We believe there is a massive shift in the minds of consumers away from pharmaceutical lab-driven products toward using natural products as functional remedies to treat and heal the human body. PLSH is well positioned and on the forefront of this movement, said Leslie Buttorff, CEO. “With this acquisition we are able to capture a high value business in the natural beverage retail and wholesale market that includes brand licensing and franchising development for all of our product segments.”

Closing of the acquisition is subject to satisfaction of customary terms and conditions for a transaction of this kind, including delivery by sellers of audited financial statements for the prior two completed fiscal years for the acquisition.

About Panacea Life Sciences Holdings, Inc.

Panacea Life Sciences Holdings, Inc. (PLSH) is holding company structured to develop and facilitate manufacturing, research, product development and distribution in the high-growth, natural human and animal health & wellness market segment. Its subsidiary, Panacea Life Sciences, Inc. (PLS) is a woman-founded and led company dedicated to manufacturing, distribution, research and production of the highest-quality nutraceutical, cannabinoid, mushroom, kratom and other natural, plant-based ingredients and products. PLS operates out of a 51,000 square foot, state-of-the-art, cGMP facility in Golden Colorado. If you would like more information, please visit www.panacealife.com

Cautionary Note Regarding Forward-Looking Statements

This press release contains forward-looking statements within the meaning of the Private Securities Litigation Reform Act of 1995, including statements. Forward-looking statements involve risks and uncertainties that could cause actual results to differ materially from those projected or anticipated. These risks and uncertainties include, but are not limited to, risks arising from supply chain disruptions or our ability to obtain raw materials as well as similar problems with our vendors, our ability to fulfill purchase orders on a timely manner, our ability to fully collect money for our purchase orders, the risk of customers returning our products, impact of the pandemic including new variants on our workforce, as well as those risks and uncertainties described by us in our annual report on Form 10-K for the fiscal year ended December 31, 2022 under the heading “Risk Factors”. Any forward-looking statement made by us herein speaks only as of the date on which it is made. Factors or events that could cause our actual results to differ may emerge from time to time, and it is not possible for us to predict all of them. We undertake no obligation to publicly update any forward-looking statement, whether as a result of new information, future developments, or otherwise, except as may be required by law.

Contact:

[email protected]

800-985-0515

Panacea’s Cannabinoid Research Center at Colorado State University makes revolutionary progress in year one

Panacea Life Sciences’ Cannabinoid Research Center (CRC) at Colorado State University (CSU) celebrates its first year of operation this month. With a mission of performing research to solve important industry issues and to better understand how cannabinoids work in the body, the center has made remarkable progress in its inaugural year. The CRC, established through collaboration between CSU and Panacea Life Sciences, consists of analytical chemistry and preparative chemistry technologies crucial for detection and purification of cannabinoids. Using these technologies, the CRC is able to remove common contaminants from hemp products, purify low concentration cannabinoids, and to support clinical studies.

The Center’s activities are coordinated by Boettcher Investigator Professor Melissa Reynolds with operations led by Jamie Cuchiaro, a Ph.D. candidate who will matriculate next month! A year ago, the CRC was a concept consisting of a new laboratory in the Colorado State University’s College of Natural Sciences and equipment still packed into crates. Over the last 12 months the laboratory has been extremely productive through initial analytical research and supporting numerous clinical studies in both dogs and humans.

 

Solving Industry Issues

Cannabis sativa L., or industrial hemp, is a cannabis plant strain specifically bred to contain low concentrations of tetrahydrocannabinol (THC) — less than 0.3%. THC is the psychogenic cannabinoid that causes the high associated with marijuana use. Due to its low propensity for inebriation and large economic impact to farmers and the health and wellness industries, industrial hemp was only recently legalized in the 2018 Farm Bill. The hemp plant is a hyperaccumulator, meaning trace elements in the soil in which the plant is grown, such as heavy metals, pesticides, and others, are readily absorbed in the plant, potentially contaminating hemp oil and rendering the material unusable. Pesticide contamination is a common issue with hemp growers. Although growers may use organic farming practices, a neighboring corn field sprayed with pesticides using a crop duster may drift the pesticide over the hemp field and be enough to result in substantial pesticide contamination. Using analytical techniques, graduate student, Jamie Cuchiaro has developed a method for complete removal of commonly used pesticides to remediate contaminated hemp oil to produce a safe and usable hemp product. This work has been submitted for publication to the Journal of Cannabis Research in August of this year.

 

Sustainability and Access to Minor Cannabinoids

The Cannabis plant has an incredibly rich chemical profile containing over 500 unique chemicals identified and over 120 cannabinoids. Of the cannabinoids, the best known due to their elevated expression in the plant, are CBD and THC. CBD, a non-psychogenic cannabinoid, is becoming commonly used by the health and wellness industry primarily as an anti-inflammatory. Each of the other 118 cannabinoids are anticipated to have unique and beneficial health benefits. The issue is determining how to obtain sufficient quantities and purity of the low concentration (minor) cannabinoids as they are present at less than 1% in hemp extracts.

One solution to obtaining sufficient quantities of minor cannabinoids has been developed in a collaboration between Panacea Life Sciences and the CRC. The process of distilling crude hemp oil into CBD distillates creates a byproduct mixture of fats, waxes, starches, and other components of the hemp plant that has the consistency and appearance of road tar. Typically, this material is thrown away to enter the waste stream. As a member of Colorado’s Environmental Leadership Program, Panacea wanted to find another use of this distillate byproduct by repurposing the material. In closer examination of the byproduct, the CRC determined that there are substantial minor cannabinoids such as cannabidivarin (CBDV), Cannabichromene (CBC), Cannabicyclol (CBL), and Cannabielsoin (CBE). The technology in the center will allow the group to further study these cannabinoids to better understand how these rare cannabinoids function in the body. This application of the CRC technology not only allows for access to these low abundance cannabinoids but also provides a solution to assist Panacea in attaining its sustainability goals by decreasing waste streams.

 

Supporting Clinical Trials

Two of the most common questions facing the industrial hemp industry are, what health benefits are provided by cannabinoids, and what concentrations/doses are needed to see health improvements? Although almost all CBD companies claim that CBD heals everything from Alzheimer’s to yeast infections, there is no guidance on dosing or really any concrete evidence that CBD does in fact help improve specific health conditions. Additionally, such companies also do not assert the measurement of how much CBD gets into the body to produce the stated effect. In order for a dietary supplement or drug to have effect in the body, a specific amount needs to be absorbed into the body. Cannabinoids, when taken orally, have very low bioavailability, meaning that less than 10% of the consumed dose will be absorbed into the body. Furthermore, the variability in bioavailability from one person to another can depend on whether cannabinoids are better absorbed when taken with or without food, individual genetics, and the dose form of the cannabinoid (edible, softgel, tablet, vape, liquid tincture, etc.). Taken together, this creates a confusing situation where cannabinoids such as CBD may work for some people and not others.

To gain further insight on cannabinoid activity, Panacea and the CRC are collaborating to launch specific clinical trials in several areas. Each study is supported by determination of the level of cannabinoids in the blood stream which will greatly improve the understanding of how cannabinoids as dietary supplements may provide health benefits. The first two studies have launched this year (2022):

  1. In collaboration with Dr. Stephanie McGrath and Dr. Julie Moreno, to examine CBD effects in a translational model of Alzheimer’s disease. In this study, performed in aged dogs that have cognitive impairment very similar to human AD, not only will CBD be evaluated for ability to slow disease progression, but will be one of the first studies to correlate how much consumed CBD enters the brain.
  2. In collaboration with Dr. Larry Good, a practicing gastroenterologist in New York, Panacea and the CRC have launched an open label study evaluating CBD and CBG for effects on irritable bowel syndrome, a condition affecting over 30 million American with no proven treatment.

The studies with doctors McGrath, Moreno, and Good, illustrate additional progress of the CRC to serve as a foundation for collaboration both within CSU as well as with other physicians and institutions. Additional collaborations in progress include that of Dr. Hollis Karoly (CSU) to explore CBD effects on anxiety and to support Dr. Karoly’s work on alcohol addiction, as well as with Camille Hoffman-Shuler at CU Anschutz to study the ability of cannabinoids to improve chronic pelvic pain and vulvodynia, a large unmet medical need in women’s health.

 

Looking Ahead

The CRC is actively working on expanding collaborations to progress research on various cannabinoids with a focus on improving health and addressing unmet medical needs. Collaborations to evaluate cannabinoids’ effects on various conditions, including exercise performance and recovery, gout, and even Post Traumatic Stress Disorder (PTSD), are underway. Panacea and the CRC also plan to work on improving methods for detecting cannabinoids as well as launching clinical studies for gout, eczema, rosacea, and acne, among others.

 

The progress made in the past year by the CRC has been tremendous and the future is extremely bright. With continued teamwork and direct studies, the CRC is poised to make even more revolutionary contributions to understanding how cannabinoids influence health and refining which conditions and doses are required for positive effects. Progress of the CRC will be posted as publications are submitted or clinical studies are completed on both the Colorado State University Panacea Life Sciences Cannabinoid Research Center webpage and at panacealife.com.

 

For any questions or comments, please reach out to [email protected].

Seed to Sale CBD Company Panacea Life Sciences, Inc. (PLSH) Announces Participation at White Label World Expo in Las Vegas

Company to showcase its proprietary vegan softgel manufacturing capabilities.

GOLDEN, CO / ACCESSWIRE / May 24, 2022 / Panacea Life Sciences Holdings, Inc. (OTCQB:PLSH) a Colorado, USA-based cannabinoid research and certified GMP manufacturing company, today announced that it will be attending the White Label World Expo in Las Vegas at the Convention Center from May 25-26, 2022. Panacea will be showcasing its broad capabilities live during the Expo at Booth #5038.

Panacea Life Sciences will be highlighting its newly acquired, proprietary vegan softgel capabilities as well as the launch of a new pet treat line. While Panacea’s main focus is CBD manufacturing, the Company has the expertise and capabilities to perform contract manufacturing for the entire health and wellness industry for humans and companion animals, including cannabinoid products, nutraceuticals, and other high-end dietary supplements.

With specialties in softgel manufacturing, Panacea has the ability to produce 1.5M softgels per day and can also produce 10,000 liquid fills per day. The Company provides full-range services from R&D and custom formulation to manufacturing and fulfillment from its 51,000 square foot facility located in Golden, Colorado.

The White Label World Expo is billed as the premiere destination for thousands of global leaders, entrepreneurs, online sellers, retailers and distributors to come together with businesses, e-commerce providers and startup owners. Panacea Life Sciences is all ready to go and will be at booth #5038 on May 25th & May 26th from 10 am-5 pm.

More details about the show can be found at whitelabelexpo.com.

About Panacea Life Sciences Holdings, Inc.

Panacea Life Sciences Holdings, Inc. is a seed to sale cannabinoid manufacturer and research company that produces purposeful, natural medicine for consumers and pets. Panacea sells softgels, gummies, tinctures, sublingual tablets, cosmetics, and other topicals. If you would like more information about this topic or to learn more about Panacea and its products or our land-to-brand practices, please visit www.panacealife.com.

Cautionary Note Regarding Forward-Looking Statements

This press release contains forward-looking statements within the meaning of the Private Securities Litigation Reform Act of 1995, including statements regarding the effectiveness of CBD and other cannabinoids improving the lives of people and pets. You can identify forward-looking statements by use of the words “may,” “will,” “should,” “plans,” “explores,” “expects,” “anticipates,” “continue,” “estimate,” “project,” “intends,” and similar expressions. Forward-looking statements involve risks and uncertainties that could cause actual results to differ materially from those projected or anticipated. These risks and uncertainties include, but are not limited to, risks arising from supply chain disruptions on our ability to obtain raw materials as well as similar problems with our vendors, the impact of the pandemic including new variants on the national and global economy, the impact on the Russian invasion of Ukraine on the global economy, lack of available funding at sufficient levels to meet our working capital needs, competition from third parties; intellectual property rights of third parties; regulatory constraints, including the need for FDA approval under certain circumstances; and changes in technology and methods of marketing; as well as those risks and uncertainties described by us in our annual report on Form 10-K for the fiscal year ended December 31, 2021 under the heading “Risk Factors”. Any forward-looking statement made by us herein speaks only as of the date on which it is made. Factors or events that could cause our actual results to differ may emerge from time to time, and it is not possible for us to predict all of them. We undertake no obligation to publicly update any forward-looking statement, whether as a result of new information, future developments, or otherwise, except as may be required by law.

Contact

Nick Cavarra
[email protected]

SOURCE: Panacea Life Sciences, Inc

Panacea Life Sciences Quarterly report

UNITED STATES

SECURITIES AND EXCHANGE COMMISSION

Washington, D.C. 20549

 

FORM 10-Q

 

(Mark One)

 

 QUARTERLY REPORT PURSUANT TO SECTION 13 OR 15(d) OF THE SECURITIES EXCHANGE ACT OF 1934

 

For the quarterly period ended: March 31, 2022

 

 TRANSITION REPORT PURSUANT TO SECTION 13 OR 15(d) OF THE SECURITIES EXCHANGE ACT OF 1934

 

For the transition period from _____________ to _____________

 

Commission File Number: 001-38190

 

Panacea Life Sciences Holdings, Inc.

(Exact name of registrant as specified in its charter)

 

Nevada   27-1085858
(State or other jurisdiction of (I.R.S. Employer
incorporation or organization) Identification No.)

 

5910 S University BlvdC18-193Greenwood VillageCO 80121

(Address of principal executive offices, Zip Code)

 

800985-0515

(Registrant’s telephone number, including area code)

 

Securities registered pursuant to Section 12(b) of the Act:

 

Title of each class Trading Symbol(s) Name of each exchange on which registered
N/A N/A N/A

 

Indicate by check mark whether the registrant (1) has filed all reports required to be filed by Section 13 or 15(d) of the Exchange Act of 1934 during the past 12 months (or for such shorter period that the registrant was required to file such reports), and (2) has been subject to such filing requirements for the past 90 days. Yes ☒ No ☐

 

Indicate by check mark whether the registrant has submitted electronically, every Interactive Data File required to be submitted pursuant to Rule 405 of Regulation S-T (§ 232.405 of this chapter) during the preceding 12 months (or for such shorter period that the registrant was required to submit such files). Yes ☒ No ☐

 

Indicate by check mark whether the registrant is a large accelerated filer, an accelerated filer, a non-accelerated filer, a smaller reporting company or an emerging growth company. See the definitions of “large accelerated filer,” “accelerated filer”, “smaller reporting company” and “emerging growth company” in Rule 12b-2 of the Exchange Act.

 

Large Accelerated Filer ☐ Accelerated Filer ☐
Non-Accelerated Filer ☒ Smaller reporting company 
Emerging growth company 

 

If an emerging growth company, indicate by check mark if the registrant has elected not to use the extended transition period for complying with any new or revised financial accounting standards provided pursuant to Section 13(a) of the Exchange Act. 

 

Indicate by check mark whether the registrant is a shell company (as defined in Rule 12b-2 of the Exchange Act). Yes ☐ No ☒

 

State the number of shares outstanding of each of the issuer’s classes of common stock, as of the latest practicable date: 14,965,317 shares of common stock, par value $0.0001 per share, outstanding as May 2, 2022.

 

All share and per share numbers have been retroactively adjusted to give effect to a 1-for-28 reverse stock split effective October 25, 2021

 

 

 

 

 

TABLE OF CONTENTS

 

Page
PART I – FINANCIAL INFORMATION
Item 1. Financial Statements 3
Item 2. Management’s Discussion and Analysis of Financial Condition and Results of Operations 25
Item 3. Quantitative and Qualitative Disclosures About Market Risk 31
Item 4. Controls and Procedures 31
PART II – OTHER INFORMATION
Item 1. Legal Proceedings 32
Item 1A. Risk Factors 32
Item 2. Unregistered Sales of Equity Securities and Use of Proceeds 32
Item 3. Defaults Upon Senior Securities 32
Item 4. Mine Safety Disclosures 32
Item 5. Other Information 32
Item 6. Exhibits 33
Signatures 34

 

 

2

 

 

PART I. FINANCIAL INFORMATION

 

ITEM 1. Financial Statements.

 

Panacea Life Sciences Holdings, Inc. and Subsidiary

Consolidated Balance Sheets

 

March 31, 2022 December 31, 2021
ASSETS
CURRENT ASSETS:
Cash and cash equivalents $ 55,997 $ 19,774
Accounts receivable, net 162,618 244,496
Other receivables, related party 500,000 500,000
Inventory 4,324,787 4,264,277
Marketable securities related party 2,846,679 3,791,483
Prepaid expenses and other current assets 233,613 278,328
TOTAL CURRENT ASSETS 8,123,694 9,098,358
Operating lease right-of-use asset, net, related party 3,507,887 3,595,100
Property and equipment, net 8,543,360 8,839,982
Intangible assets, net 46,051 61,401
Goodwill 2,188,810 2,188,810
TOTAL ASSETS $ 22,409,802 $ 23,783,651
LIABILITIES AND STOCKHOLDERS’ EQUITY
CURRENT LIABILITIES:
Accounts payable and accrued expenses $ 2,151,199 $ 1,685,825
Operating lease liability, current portion, related party 1,740,594 1,624,090
Note payable-current, related party 6,923,857 6,441,866
Convertible note payable, net 642,638 220,005
Paycheck protection loan, SBA Loan 99,100 99,100
TOTAL CURRENT LIABILITIES: 11,557,388 10,070,886
Operating lease liability, long-term portion, related party 3,258,312 3,347,335
Other long-term liabilities, related party 3,413,309 3,263,028
TOTAL LIABILITIES 18,229,009 16,681,249
Commitments and contingencies
STOCKHOLDERS’ EQUITY
Series A Preferred Stock: $0.0001 Par Value, 1,000 shares designated; 0 and 350 shares issued and outstanding on March 31, 2022 and December 31, 2021 respectively.
Series B-1 Preferred: $0.0001 Par Value, 32,000,000 shares designated; 1,500,000 and 1,500,000 shares issued and outstanding on March 31, 2022 and December 31, 2021 respectively. 150 150
Series B-2 Preferred: $0.0001 Par Value, 6,000,000 shares designated; 6,000,000 and 6,000,000 shares issued and outstanding on March 31, 2022 and December 31, 2021 respectively. 600 600
Series C Preferred: $0.0001 Par Value, 1,000,000 shares designated; 1,000,000 and 1,000,000 shares issued and outstanding on March 31, 2022 and December 31, 2021 respectively. 100 100
Series C-1 Preferred: $0.0001 Par Value, 10,000 shares designated; 10,000 and 10,000 shares issued and outstanding on March 31, 2022 and December 31, 2021 respectively. 1 1
Series C-2 Preferred: $0.0001 Par Value, 10,000 shares designated; 10,000 and 10,000 shares issued and outstanding on March 31, 2022 and December 31, 2021 respectively. 1 1
Series D Preferred: $0.0001 Par Value, 10,000 shares designated; 10,000 and 10,000 shares issued and outstanding on March 31, 2022 and December 31, 2021 respectively. 1 1
Common Stock: $0.0001 Par Value, 650,000,000 shares authorized; 14,762,342 and 14,073,708 shares issued and outstanding on March 31, 2022 and December 31, 2021 respectively. 1,476 1,407
Additional paid in capital 23,725,724 23,865,155
Accumulated deficit (19,547,259 ) (16,765,013 )
TOTAL STOCKHOLDERS’ EQUITY 4,180,794 7,102,402
TOTAL LIABILITIES AND STOCKHOLDERS’ EQUITY $ 22,409,802 $ 23,783,651

 

The accompanying notes are an integral part of these unaudited condensed consolidated financial statements.

 

3

 

 

Panacea Life Sciences Holdings, Inc. and Subsidiary

Consolidated Statements of Operations

 

Three Months Ended March 31,
2022 2021
REVENUE $ 466,474 $ 512,138
COST OF SALES 366,091 329,837
GROSS PROFIT 100,383 182,301
OPERATING EXPENSES
Operating expenses 1,287,817 987,935
General and administrative expenses 460,550 286,042
TOTAL OPERATING EXPENSES 1,748,367 1,273,977
LOSS FROM OPERATIONS (1,647,984 ) (1,091,674 )
OTHER INCOME (EXPENSES)
Interest expense (501,295 ) (322,563 )
Unrealized gain (loss) on marketable securities, net (944,804 ) 1,413,749
Employer retention credit 253,791
Rental Income 58,046 95,601
Gain on extinguishment of debt 275,539
TOTAL OTHER INCOME (EXPENSE) (1,134,262 ) 1,462,326
INCOME (LOSS) BEFORE INCOME TAXES (2,782,246 ) 370,650
TAXES
NET INCOME (LOSS) $ (2,782,246 ) $ 370,650
Per-share data
Basic net income (loss) per share $ (0.19 ) $ 0.02
Diluted net income (loss) per share $ (0.19 ) $ 0.02
Weighted average number of common shares outstanding (Basic) 14,762,342 16,915,706
Weighted average number of common shares outstanding (Diluted) 14,762,342 21,897,959

 

The accompanying notes are an integral part of these unaudited condensed consolidated financial statements.

 

4

 

 

Panacea Life Sciences Holdings, Inc. and Subsidiary

Consolidated Statements of Stockholders’ Equity

 

Preferred Stock Common Stock Additional Paid-in Accumulated Total Stockholder’s
Shares Amount Shares Amount Capital Deficit Equity
Balance as of December 31, 2021 8,530,350 $ 853 14,073,708 $ 1,407 $ 23,865,155 $ (16,765,013 ) $ 7,102,402
Issuance of shares in respect of the merger 679,694 68 (68 )
Issuance of common stock for services 8,940 1 19,999 20,000
Conversion of Series A Preferred Stock to convertible debt and warrants (350 ) (159,362 ) (159,362 )
Net Income (Loss) (2,782,246 ) (2,782,246 )
Balance as of March 31, 2022 8,530,000 $ 853 14,762,342 $ 1,476 $ 23,725,724 $ (19,547,259 ) $ 4,180,794
Balance as of December 31, 2020 1,020,000 $ 102 16,915,706 $ 1,692 $ 18,689,119 $ (11,982,614 ) $ 6,708,299
Net Income 370,650 370,650
Balance as of March 31, 2021 1,020,000 $ 102 16,915,706 $ 1,692 $ 18,689,119 $ (11,611,964 ) $ 7,078,949

 

The accompanying notes are an integral part of these unaudited condensed consolidated financial statements

 

5

 

 

Panacea Life Sciences Holdings, Inc. and Subsidiary

Consolidated Statements of Cash Flows

 

For the months ended March 31,
2022 2021
Cash flows from operating activities
Net loss $ (2,782,246 ) $ 370,650
Adjustments to reconcile net loss to net cash used in operating activities
Depreciation 408,690 427,522
Unrealized gain on marketable securities 944,804 (1,413,749 )
Amortization of intangible assets 15,350 15,350
Amortization of debt discount and non-cash interest expense 263,271
Gain on forgiveness of payroll protection loan (273,300 )
Changes in operating assets and liabilities
Accounts receivable 81,878 (133,160 )
Inventory (60,510 ) (326,497 )
Prepaid expense and other assets 44,715 (13,321 )
Accounts payable and accrued expenses 533,312 436,583
Operating lease liability, net 114,694 114,694
Net cash used in operating activities (436,043 ) (795,228 )
Cash flows from investing activities
Net fixed asset acquisitions (9,725 ) (86,769 )
Net Cash provided by (used in) investing activities (9,725 ) (86,769 )
Cash flows from financing activities
Proceeds from payroll protection loan – related party 243,041
Payments of principal on notes payable (230,201 ) (115,000 )
Proceeds from Note payable-related party 712,192 767,000
Cash provided by financing activities 481,991 895,041
Net increase (decrease) in Cash and Cash Equivalents 36,223 13,044
Cash and Cash Equivalents, Beginning of Period 19,774 84,379
Cash and Cash Equivalents, End of Period $ 55,997 $ 97,423
Noncash investing and financing activity
Conversion of Preferred A shares to Note Payable 385,000
Capitalized assets purchased on account – related party $ 102,344 $ 120,170

 

The accompanying notes are an integral part of these unaudited condensed consolidated financial statements.

 

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PANACEA LIFE SCIENCES HOLDINGS, INC. AND SUBSIDIARY

NOTES TO UNAUDITED CONDENSED CONSOLIDATED FINANCIAL STATEMENTS

MARCH 31, 2021

 

NOTE 1 – NATURE OF ORGANIZATION

 

Organization and Business Description

 

PANACEA LIFE SCIENCES HOLDINGS, Inc. (the “Company”, “we”, “us”, “our”) was incorporated on January 18, 2008 in the State of Nevada. In January 2019, the Company added to the scope of its business activities, efforts to produce, market and sell products made from industrial hemp containing cannabidiol (“CBD”). On June 30, 2021 the Company entered into a Securities Exchange Agreement (the “Exchange Agreement”) with Panacea Life Sciences, Inc., (“Panacea”) a seed to sale CBD company, and the stockholders of Panacea. Pursuant to the Exchange Agreement, the former Panacea stockholders assumed majority control of the Company and all operations are now operated by Panacea, which as a result of the share exchange, became a wholly-owned subsidiary of the Company. In October 2021, the Company changed its name from Exactus Inc. to Panacea Life Sciences Holdings, Inc.

 

The Company is a GMP certified, seed-to-sale cannabinoid and nutraceutical manufacturer and research company that produces purposeful, natural pharmaceutical alternatives for consumers and pets. In addition to manufacturing raw materials from industrial hemp, we custom formulate and manufacture softgels (both bovine and vegan), gummies, tinctures, sublingual tablets, patches, K-Tape, topical pain relief and skin care products. Panacea was founded by Leslie Buttorff in 2017 as a woman-owned business, was formed to own and engage in creating disruptive healthcare and veterinary natural relief products to make a difference in the lives of humans and pets.

 

NOTE 2 – SUMMARY OF SIGNIFICANT ACCOUNTING POLICIES

 

Basis of presentation and principles of consolidation

 

The Company’s consolidated financial statements include the financial statements of Panacea Life Sciences, Inc., a wholly owned subsidiary acquired on June 30, 2021.

 

The accompanying consolidated financial statements have been prepared in accordance with generally accepted accounting principles in the United States of America and the rules and regulations of the United States Securities and Exchange Commission (the “SEC”) for interim financial information, which includes consolidated unaudited interim financial statements and present the consolidated unaudited interim financial statements of the Company and its wholly-owned subsidiary as of March 31, 2022. Accordingly, they do not include all of the information and notes required by accounting principles generally accepted in the United States of America. All intercompany transactions and balances have been eliminated. In the opinion of management, all adjustments necessary to present fairly our financial position, results of operations, stockholders’ equity and cash flows as of March 31, 2022, and 2021, and for the periods then ended, have been made. Those adjustments consist of normal and recurring adjustments. Operating results for the three ended March 31, 2022 and 2021 are not necessarily indicative of the results that may be expected for any subsequent quarters or for the year ending December 31, 2022. Certain information and note disclosures normally included in our annual financial statements prepared in accordance with generally accepted accounting principles have been condensed or omitted.

 

 

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Going concern

 

These unaudited condensed consolidated financial statements are presented on the basis that the Company will continue as a going concern. Panacea has combined with Panacea Life Sciences Holdings, Inc. (formerly Exactus), so the below items reflect the consolidated company. The going concern concept contemplates the realization of assets and satisfaction of liabilities in the normal course of business. Since our inception in later 2017, we have generated losses from operations. As of March 31, 2022, our accumulated deficit was $19.5 million, and we had $2.903 million in cash and liquid stock. As of March 31, 2022 the shares of common stock we hold in 22nd Century Group, Inc. (1,227,017 shares) ( Nasdaq: XXII) (“XXII”) was valued at approximately $2.847 million. The XXII stock is pledged to secure a $4.063 million promissory note in favor of Quintel-MC, Incorporated (“Quintel”) and a $1.624 million promissory note in favor of Leslie Buttorff, CEO of the Company. Quintel-MC, Inc. is owned by the CEO. These items are shown on the balance sheet as related party loans. The current plan with respect to the XXII stock is to hold this stock during the short-term pending XXII’s application for MRTP FDA approval. These factors raise doubt about the Company’s ability to continue as a going concern for a period of 12 months from the issuance date of this report. Management cannot provide assurance that the Company will ultimately achieve or maintain profitable operations or become cash flow positive or raise additional debt and/or equity capital. In addition, due to insufficient revenue, we will need to obtain further funding through public or private equity offerings, debt financing, collaboration arrangements or other sources in order to maintain active business operations. We currently do not have sufficient cash flow to pay our ongoing financial obligations on a consistent basis. The issuance of any additional shares of Common Stock, preferred stock or convertible securities could be substantially dilutive to our shareholders. In addition, adequate additional funding may not be available to us on acceptable terms, or at all. These unaudited condensed consolidated financial statements do not include any adjustments related to the recoverability and classification of assets or the amounts and classification of liabilities that might be necessary should the Company be unable to continue as a going concern. In November 2021, the Company closed a $1.1 million convertible note and warrants financing and received $1 million.

 

COVID-19

 

 

The COVID-19 pandemic has resulted in a global slowdown of economic activity which may reduce the future demand for a broad variety of goods and services, while also disrupting sales channels, marketing activities and supply chains. The Company’s business operations have been negatively impacted by the COVID-19 pandemic and related events. While the lockdowns and disruptions have largely ended, we cannot predict whether future variants will cause adverse consequences. However, recent supply chain disruptions and delays may hinder our ability to continue our operations and generate revenue. The impact to date has included a decline in CBD product and sales demand. Further, in 2020, the Company (Panacea) invested in personal protective equipment (PPE) materials to sell hand sanitizers, testing kits and masks, and sales of PPE products, which constituted a significant portion of our revenue during the fiscal quarter ended June 30, 2021 and prior periods. These revenues have declined as vaccines continue to be administered and mask mandates and similar requirements have been lifted or reduced in many places. Although the Company is unable to predict the full impact and duration of COVID-19 on its business, the Company is actively managing its financial expenditures in response to the current uncertainty.

 

The impact of the COVID-19 pandemic and related events, including actions taken by various government authorities in response, have increased market volatility and make the estimates and assumptions that affect the amounts reported in the financial statements and accompanying notes more difficult. As of the date of issuance of the financial statements, the Company is not aware of any specific event or circumstance that would require it to update its estimates, judgments or revise the carrying value of its assets or liabilities. These estimates may change, as new events occur and additional information is obtained, and are recognized in the condensed consolidated financial statements as soon as they become known.

 

 

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Use of Estimates

 

The Unaudited Condensed Consolidated Financial Statements have been prepared in conformity with US GAAP and required management of the Company to make estimates and assumptions in preparation of these statements. Actual results may differ significantly from those estimates. Significant estimates made by management include but are not limited to the useful life of property and equipment, incremental borrowing rate used in the calculation of right of use asset and lease liability, reserves for inventory, allowance for doubtful accounts, revenue allocations, valuation allowance on deferred tax assets, assumptions used in assessing impairment of long-term assets, assumptions used in the calculation of net realizable value of inventory and fair value of non-cash equity transactions.

 

Cash and Cash Equivalents

 

For purposes of balance sheet presentation and reporting of cash flows, the Company considers all unrestricted demand deposits, money market funds and highly liquid debt instruments with an original maturity of less than 90 days to be cash and cash equivalents. There were no cash equivalents. The Company places its cash and cash equivalents with high-quality financial institutions. At times, balances in the Company’s cash accounts may exceed the Federal Deposit Insurance Corporation (“FDIC”) limit. On March 31, 2022, the Company’s cash balances did not exceed the FDIC limit.

 

Accounts Receivable

 

Accounts receivable are generally unsecured. The Company establishes an allowance for doubtful accounts receivable based on the age of outstanding invoices and management’s evaluation of collectability. Accounts are written off after all reasonable collection efforts have been exhausted and management concludes that likelihood of collection is remote. Any future recoveries are applied against the allowance for doubtful accounts. An allowance of $10,000 was taken at the beginning of 2022 to allow for any doubtful accounts to be expensed. As of March 31, 2022 $5,850 of this allowance was expensed. The Company’s accounts receivable policy changed in 2021 to only provide larger, well-established companies with Net 30 payment terms. For all other sales they are paid by credit card or wires received before the product is shipped to the customer.

 

Inventory

 

Inventories are stated at low of cost or net realizable value. Inventories of purchased materials are valuated using a moving average method and managed by first in first out basis (FIFO). Inventories of internally manufactured materials are valuated using a standard costing method and are also managed on a FIFO basis. Production related costs that are capitalized as inventory as part of the standard cost valuation include the direct materials consumed, direct labor used, indirect labor used, and manufacturing overhead. Overhead is calculated based on specific manufacturing process and allocated on an order-by-order basis. Production variances that occur between standard cost valuation and actual costs are expensed as incurred in the income statement as part of cost of goods sold.

 

 

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Marketable securities

 

The Company’s marketable securities consists of 1,227,017 shares of XXII which are classified as available-for-sale and included in current assets as they are pledged to secure two promissory notes (see Note 2 – Going Concern). Securities are valued based on market prices for identical assets using third party certified pricing sources. Available-for-sale securities are carried at fair value with unrealized and realized gains and losses reported as a component of income (loss). Realized gains and losses, if any, are calculated on the specific identification method and are included in other income in the condensed consolidated statements of operations.

 

Fair Value Measurements

 

The Company adopted the provisions of Accounting Standard Codification (“ASC”) Topic 820, “Fair Value Measurements and Disclosures”, which defines fair value as used in numerous accounting pronouncements, establishes a framework for measuring fair value, and expands disclosure of fair value measurements. The guidance prioritizes the inputs used in measuring fair value and establishes a three-tier value hierarchy that distinguishes among the following:

 

Level 1—Valuations based on unadjusted quoted prices in active markets for identical assets or liabilities that the Company has the ability to access.
Level 2—Valuations based on quoted prices for similar assets or liabilities in active markets, quoted prices for identical or similar assets or liabilities in markets that are not active and models for which all significant inputs are observable, either directly or indirectly.
Level 3—Valuations based on inputs that are unobservable and significant to the overall fair value measurement.

 

The following table shows, by level within the fair value hierarchy, the Company’s assets and liabilities at fair value on a recurring basis as of March 31, 2022 and December 31, 2021:

 

March 31, 2022 December 31, 2021
Total Level 1 Level 2 Level 3 Total Level 1 Level 2 Level 3
Marketable securities $ 2,846,679 $ 2,846,679 $ $ 3,719,483 $ 3,719,483 $ $
Total $ 2,846,679 $ 2,846,679 $ $ $ 3,719,483 $ 3,719,483 $ $

March 31, 2022
Balance at beginning of year $ 3,791,483
Unrealized loss on marketable securities, net 944,804
Balance at end of period $ 2,846,679

As of March 31, 2022, the Company has no liabilities that are re-measured at fair value.

 

Property and Equipment

 

Property and equipment are stated at cost less accumulated depreciation. Depreciation is calculated using the straight-line method on the various asset classes over their estimated useful lives, which range from 3 to ten years when placed in service. The cost of repairs and maintenance is expensed as incurred; major replacements and improvements are capitalized. When assets are retired or disposed of, the cost and accumulated depreciation are removed from the accounts, and any resulting gains or losses are included in income in the year of disposition.

 

 

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Intangible Assets and Goodwill

 

The Company has intangible assets. Goodwill is comprised of the purchase price of business combinations in excess of the fair market value assigned at acquisition to the tangible and intangible assets acquired. Goodwill is not amortized. The Company tests goodwill for impairment on an annual basis. The Company performed its most recent goodwill impairment using a discounted cash flow analysis and found that the fair value exceeded the carrying value. It has $2.189 million of goodwill from the acquisition of the assets of Phoenix Life Sciences, Inc. (“Phoenix”) in October 2017 and intangible assets of $0.077 million as of March 31, 2022 and $0.123 million for as of December 31, 2020. In the acquisition of Phoenix, the Company acquired product formulas which is classified as an intangible asset.

  Estimated Life  
Goodwill from Phoenix Acquisition Tested Yearly for Impairment
Intangibles – Formulations 5 Years

 

March 31, 2022 December 31, 2021
Goodwill $ 2,188,810 $ 2,188,810
Intangibles – Formulations 307,001 307,001
Less accumulated amortization (260,950 ) (245,600 )
Net intangible assets $ 46,051 $ 61,401

Leases

 

The Company determines if an arrangement is a lease at inception. Contracts containing a lease are further evaluated for classification as an operating or finance lease. In determining the leases classification, the Company assesses among other criteria: (i) 75% or more of the remaining economic life of the underlying asset is a major part of the remaining economic life of that underlying asset; and (ii) 90% or more of the fair value of the underlying asset comprises substantially all of the fair value of the underlying asset. Operating leases are included in operating lease right-of-use (“ROU”) assets, other current liabilities and long-term operating lease liabilities in the Company’s consolidated balance sheets. Finance leases are included in property, plant and equipment, net, other current liabilities, and long-term finance lease liabilities in the Company’s consolidated balance sheets. ROU assets represent the right to use an underlying asset for the lease term and lease liabilities represent the Company’s obligation to make lease payments arising from the lease. For leases with terms greater than 12 months, the Company records the ROU asset and liability at commencement date based on the present value of lease payments according to their term.

 

The Company uses incremental borrowing rates based on the estimated rate of interest for collateralized borrowing over a similar term of the lease payments at commencement date. The ROU asset also includes any lease payments made and excludes lease incentives. Lease terms may include options to extend or terminate the lease when it is reasonably certain that the Company will exercise that option. Lease expenses are recognized on a straight-line basis over the lease term or the useful life of the leased asset.

 

In addition, the carrying amount of the ROU and lease liabilities are remeasured if there is a modification, a change in the lease term, a change in the in-substance fixed lease payments or a change in the assessment to purchase the underlying asset.

 

Convertible Notes Payable

 

The Company has issued convertible notes, which contain variable conversion features, whereby the outstanding principal and accrued interest automatically convert into common shares at a fixed price which may be a discount to the common stock at the time of conversion. Some of the conversion features of these notes are contingent upon future events, whereby, the holder agreed not to convert until the contingent future event has occurred.

 

 

 

 

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Revenue Recognition

 

The Company accounts for revenue in accordance with ASC Topic 606, Revenue from Contracts with Customers.

 

The Company accounts for a contract when it has been approved and committed to, each party’s rights regarding the goods or services to be transferred have been identified, the payment terms have been identified, the contract has commercial substance, and collectability is probable. Revenue is generally recognized net of allowances for returns and any taxes collected from customers and subsequently remitted to governmental authorities. However, the Company’s sales are primarily through retail stores, purchase orders or ecommerce; thus, currently contract liabilities are negligible. The Company does not have any multiple-element arrangements.

 

Some of the Company’s contract liabilities consist of advance customer payments. Contract liability results from transactions in which the Company has been paid for products by customers, but for which all revenue recognition criteria have not yet been met. Once all revenue recognition criteria have been met, the contract liabilities are recognized. The Company recorded $18,912 and $24,585 in advanced customer payments as of March 31, 2022 and December 31, 2021, respectively and these amounts are included in the balance sheet line item of accounts payable and accrued expenses.

March 31, 2022 December 31, 2021
Balance, beginning of period $ 24,585 $ 121,300
Payments received for unearned revenue 1,957 41,465
Revenue earned 7,630 138,180
Balance, end of period $ 18,912 $ 24,585

Revenue is recognized when a customer obtains control of promised goods or services and is recognized in an amount that reflects the consideration that an entity expects to receive in exchange for those goods or services. In addition, the standard requires disclosure of the nature, amount, timing, and uncertainty of revenue and cash flows arising from contracts with customers. The amount of revenue that is recorded reflects the consideration that the Company expects to receive in exchange for those goods. The Company applies the following five-step model in order to determine this amount: (i) identification of the promised goods in the contract; (ii) determination of whether the promised goods are performance obligations, including whether they are distinct in the context of the contract; (iii) measurement of the transaction price, including the constraint on variable consideration; (iv) allocation of the transaction price to the performance obligations; and (v) recognition of revenue when (or as) the Company satisfies each performance obligation.

 

Revenue related to the sale of products is recognized once goods have been sold to the customer and the performance obligation has been completed. In both contracted purchase and retail sales, we offer consumer products through our online stores. Revenue is recognized when control of the goods is transferred to the customer. This generally occurs upon our delivery to a third-party carrier or, to the customer directly. Revenue from tolling services is recognized when the performance obligation, such as processing of the material, has been completed and output material has been transferred to the customer.

 

 

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Revenue is generally recognized net of allowances for returns and any taxes collected from customers and subsequently remitted to governmental authorities. A contract liability results from transactions in which the Company has been paid for products by customers, but for which all revenue recognition criteria have not yet been met. Once all revenue recognition criteria have been met, the contract liabilities are recognized. However, the Company’s sales are primarily through retail stores, purchase orders or ecommerce; thus, currently contract liabilities are negligible. The Company does not have any multiple-element arrangements.

 

The Company also has recorded other income related to rental income it receives from leasing out space in the laboratory it occupies.

 

Shipping and Handling Costs

 

The Company accounts for shipping and handling fees in accordance with ASC 606. The amounts charged to customers for shipping products are recognized as revenues and the related freight costs of shipping products are classified in general and administrative costs as incurred. Shipping costs are included as a component of general and administrative and were $14,184 and $2,789 for the three months ended March 31, 2022 and 2021, respectively.

 

Advertising & Marketing

 

Advertising costs are expensed when incurred and are included in advertising and promotional expense in the accompanying statements of operations. Included in this category are expenses related to public relations, investor relations, new package design, website design, design of promotional materials, cost of trade shows, cost of products given away as promotional samples, and paid advertising. The Company recorded advertising costs included in general and administrative costs of $66,796 and $151,183 for the three months ended March 31, 2022 and 2021, respectively.

 

Segment Information

 

The Company follows the provisions of ASC 280-10 Segment Reporting. This standard requires that companies disclose operating segments based on the manner in which management disaggregates the Company in making internal operating decisions. Segment identification and selection is consistent with the management structure used by the Company’s chief operating decision maker to evaluate performance and make decisions regarding resource allocation, as well as the materiality of financial results consistent with that structure. Based on the Company’s management structure and method of internal reporting, the Company has one operating segment. The Company’s chief operating decision maker does not review operating results on a disaggregated basis; rather, the chief operating decision maker reviews operating results on an aggregate basis.

 

Earnings per Share

 

The Company computes basic and diluted earnings per share amounts in accordance with ASC Topic 260, “Earnings per Share”. Basic earnings per share is computed by dividing net income (loss) available to common stockholders by the weighted average number of common shares outstanding during the reporting period. Diluted earnings per share reflects the potential dilution that could occur if preferred stock converted to common stock and warrants are exercised. Preferred stock and warrants are excluded from the diluted earnings per share calculation if their effect is anti-dilutive.

 

The Business Combination on June 30, 2021 was accounted for as a recapitalization of equity structure. In October, 2021 the Company completed 1-for-28 reverse stock split. Pursuant to GAAP, the Company retrospectively recasted the weighted-average shares included within its condensed consolidated statements of operations for the three months ended March 31, 2021. The basic and diluted weighted-average Panacea ordinary shares are retroactively converted to shares of the Company’s common stock to conform to the recasted condensed consolidated statements of stockholders’ equity.

 

 

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The following financial instruments were not included in the diluted loss per share calculation for the three months ended March 31, 2022 and 2021 because their effect was anti-dilutive:

 

For the three months ended March 31,
2022 2021
Options to purchase common stock 61,446
Warrants to purchase common stock 56,377
Series B-1 Convertible Preferred 6,679
Series B-2 Convertible Preferred 26,786
Series C Convertible Preferred 2,289,220
Series C-1 Convertible Preferred 1,064,908
Series D Convertible Preferred 1,628,126
Total 5,133,541

 

 

Income Taxes

 

Income taxes are accounted for under the asset and liability method prescribed by FASB ASC Topic 740. These standards require a company to determine whether it is more likely than not that a tax position will be sustained upon examination based upon the technical merits of the position. If the more likely than not threshold is met, a company must measure the tax position to determine the amount to recognize in the financial statements. Deferred income taxes are recorded for temporary differences between financial statement carrying amounts and the tax basis of assets and liabilities. Deferred tax assets and liabilities reflect the tax rates expected to be in effect for the years in which the differences are expected to reverse. A valuation allowance is provided if it is more likely than not that some or all of the deferred tax asset will not be realized.

 

Recently Issued Accounting Standards

 

In August 2020, the Financial Accounting Standards Board (“FASB”) issued Accounting Standards Update (“ASU”) No. 2020-06, Debt with Conversion and Other Options (Subtopic 470-20) and Derivatives and Hedging-Contracts in Entity’s Own Equity (Subtopic 815-40), Accounting for Convertible Instruments and Contract’s in an Entity’s Own Equity. The ASU simplifies accounting for convertible instruments by removing major separation models required under current GAAP. Consequently, more convertible debt instruments will be reported as a single liability instrument with no separate accounting for embedded conversion features. The ASU removes certain settlement conditions that are required for equity contracts to qualify for the derivative scope exception, which will permit more equity contracts to qualify for it. The ASU simplifies the diluted net income per share calculation in certain areas. The ASU is effective for annual and interim periods beginning after December 31, 2021, and early adoption is permitted for fiscal years beginning after December 15, 2020, and interim periods within those fiscal years. The Company does not expect the adoption of ASU 2020-6 to have any material impact on its consolidated financial statements.

 

 

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In May 2021, the Financial Accounting Standards Board (“FASB”) issued ASU 2021-04 “Earnings Per Share (Topic 260), Debt—Modifications and Extinguishments (Subtopic 470-50), Compensation— Stock Compensation (Topic 718), and Derivatives and Hedging—Contracts in Entity’s Own Equity (Subtopic 815- 40) Issuer’s Accounting for Certain Modifications or Exchanges of Freestanding Equity-Classified Written Call Options” which clarifies and reduces diversity in an issuer’s accounting for modifications or exchanges of freestanding equity-classified written call options (for example, warrants) that remain equity classified after modification or exchange. An entity should measure the effect of a modification or an exchange of a freestanding equity-classified written call option that remains equity classified after modification or exchange as follows: i) for a modification or an exchange that is a part of or directly related to a modification or an exchange of an existing debt instrument or line-of-credit or revolving-debt arrangements (hereinafter, referred to as a “debt” or “debt instrument”), as the difference between the fair value of the modified or exchanged written call option and the fair value of that written call option immediately before it is modified or exchanged; ii) for all other modifications or exchanges, as the excess, if any, of the fair value of the modified or exchanged written call option over the fair value of that written call option immediately before it is modified or exchanged. The amendments in this Update are effective for all entities for fiscal years beginning after December 15, 2021, including interim periods within those fiscal years. An entity should apply the amendments prospectively to modifications or exchanges occurring on or after the effective date of the amendments. The Company is currently evaluating the impact of this standard on its consolidated financial statements.

 

The Company does not discuss recent pronouncements that are not anticipated to have an impact on or are unrelated to its financial condition, results of operations, cash flows or disclosures.

NOTE 3 – PROPERTY, EQUIPMENT, NET OF ACCUMULATED DEPRECIATION

 

Property and equipment, net including any major improvements, are recorded at historical cost. The cost of repairs and maintenance is charged against operations as incurred. Depreciation is calculated using the straight-line method over the estimated useful lives of the related assets, generally as follows:

  Estimated Life  
Computers and technological assets 3 – 5 Years
Furniture and fixtures 3 – 5 Years
Machinery and equipment 5 – 10 Years
Leasehold improvement 10 Years

Property and equipment, net consists of the following:

 

March 31, 2022 December 31, 2021
Computers and technological assets $ 3,616,765 $ 3,514,421
Furniture and fixtures 55,950 55,950
Machinery and equipment 7,531,387 7,530,787
Land 92,222 92,222
Leasehold improvements 1,508,915 1,508,915
Total 12,805,239 12,702,295
Less accumulated depreciation (4,261,879 ) (3,862,313 )
Total property and equipment, net $ 8,543,360 $ 8,839,982

Depreciation expenses for the three-month period ended March 31, 2022 and 2021 were $408,690 and $427,522 respectively.

 

 

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NOTE 4 – INVENTORY

 

Inventory consists of the following components:

 

March 31, 2022 December 31, 2021
Raw Materials $ 937,108 $ 970,393
Semi-Finished 1,552,243 1,466,763
Finished Goods 1,819,887 1,805,779
Packaging 15,549 15,549
Trading 5,793
Total $ 4,324,787 $ 4,264,277

Inventories are stated at lower of cost or net realizable value using the standard costing method for its work in process and finished goods. For its raw materials, trading goods, and packaging supplies, the Company utilizes the moving average method for costing purposes and FIFO. At this time there are no inventory reserves required.

 

NOTE 5 –OPERATING LEASE RIGHT-OF-USE ASSETS AND OPERATING LEASE LIABILITIES – RELATED PARTY

 

Right of Use

 

The Company adopted Accounting Standards Update (“ASU”) No. 2016-02, “Leases” (“ASC 842”) on January 1, 2019, the start of our 2019 fiscal year. The Company has one lease arrangement with a related party entered into on December 22, 2018 for 3-year term starting with January 1, 2019 for certain laboratory facilities, with a nine-year extension option. This lease was extended and now expires on December 31, 2030. At inception, the Company recognized a Right of Use Asset and a corresponding lease liability in the amount of $4,595,509. The Company’s lease arrangements may contain both lease and non-lease components. The Company has elected to combine and account for lease and non-lease components as a single lease component. The Company has incorporated residual value obligations in leases for which there is such occurrences. Regarding short-term leases, ASC 842-10-25-2 permits an entity to make a policy election not to apply the recognition requirements of ASC 842 to Short-term leases. The Company has elected not to apply the ASC 842 recognition criteria to any leases that qualify as Short-Term Leases.

 

The Company leases a portion of the property (formerly the Environmental Protection Agency building) in Golden, CO from J&N Real Estate, owned by the CEO, a related party with a term expiring on December 31, 2030. The lease consists of all laboratory space including testing facilities, water treatment, extraction and production. The lease of the property is based on the fair market rent and triple net lease (NNN) values competitive in the marketplace for a cGMP facility. The Company also subleases some of its laboratory space to other CBD companies. This income is presented under the Other Income line items of the statements of operations. The leases vary from short-term monthly leases to 3-year leases but are all cancellable.

 

 

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Below is a summary of our right of use assets and liabilities as of March 31, 2022.

 

March 31, 2022 December 31, 2021
Right-of-use assets $ 3,507,887 $ 3,595,100
Present value of operating lease liabilities $ 3,607,095 $ 3,692,392
Less: Long-term portion of operating lease liability (3,258,312 ) (3,347,335 )
Short-term portion of operating lease liability 348,783 345,057
Unpaid balances 1,391,811 1,279,033
Total short-term lease liability obligations $ 1,740,594 $ 1,624,090
Weighted-average remaining lease term (Ends December 31, 2030)  

8.75 years

 

9 years

Weighted-average discount rate 3.0 %

During the three months ended March 31, 2022 and 2021, we recognized approximately $114,693 respectively in operating lease costs. Operating lease costs are included in operating expenses in our consolidated statement of operations.

 

Approximate future minimum lease payments for our right of use assets over the remaining lease periods as of March 31, 2022, are as follows:

 

2022 338,333
2023 455,622
2024 460,178
2025 464,780
2026 469,427
Thereafter 1,925,123
Total undiscounted operating lease payments 3,887,908
Less: Imputed interest (506,368 )
Present value of operating lease liabilities $ 3,607,095

NOTE 6 – NOTES PAYABLE

 

Convertible Note Payable

 

On November 18, 2021, the Company entered into a Securities Purchase Agreement (“SPA”) with Lincoln Park Capital Fund, LLC (the “Purchaser”) pursuant to which the Company agreed to sell a 10% original issue discount senior convertible promissory note in the principal amount of $1,100,000 (the “Convertible Note”) and five-year warrants to purchase 785,715 shares of the Company’s common stock, par value $0.0001 per share at an exercise price of $1.40 per share (the “Warrants”) pursuant to the terms and conditions of the SPA for a total purchase price of $1,000,000.

 

The Note will be due November 18, 2022, which is one year from the issuance date. The Note initially does not bear any interest, however upon and during any event of default by the Company, the Note will accrue interest at a rate of 18% per annum. Events of default include the failure to file all required reports and other documents with the SEC pursuant to Exchange Act by January 2022, suspension of trading or quotation of the Company’s common stock on the OTCQB or a national securities exchange, and failure to reserve a sufficient number of shares for the conversion or exercise of all securities sold under the SPA. Further, upon an event of default, the holder will have the right to cause the Company to redeem the outstanding principal and accrued interest on the Note at a 125% premium.

 

 

17

 

 

The principal and accrued interest on the Note is convertible into common stock at a conversion price of $1.40 per share, subject to certain adjustments summarized as follows: (i) if an event of default has occurred prior to the maturity date, a reduction to 80% of the conversion price then in effect, (iii) anti-dilution adjustment upon certain issuances of common stock or derivative securities at a price per share that is lower than the conversion price, (iii) customary adjustments for stock splits, stock dividends and similar corporate events, and (iv) adjustment upon a public offering by the Company meeting certain delineated criteria, as summarized below.

 

Under the terms of the Note, upon a public offering by the Company of common stock, either alone or in units or with other securities pursuant to an effective registration statement resulting in gross proceeds to the Company of at least $10,000,000, and in connection with which the common stock is approved for listing listed on a national securities exchange (a “Qualified Offering”), the conversion price will be reduced to 90% of the offering price per share in the Qualified Offering, if that price is lower than the conversion price then in effect. Additionally, immediately prior to a Qualified Offering, the Company may redeem all or part of the outstanding principal and accrued interest on the Note at a 115% premium.

 

The Note also contains customary negative covenants prohibiting the Company from certain actions while the Note remains outstanding.

 

The Warrants will be exercisable for a five-year term beginning on May 18, 2022, at an exercise price of $1.40 per share, subject to certain adjustments which are substantially similar to those contained in the Note, including the Qualified Offering adjustment.

 

Each of the Note and the Warrants contain a 4.99% beneficial ownership limitation pursuant to which neither may be converted or exercised, as applicable, if and to the extent that following such conversion or exercise the holder would beneficially own more than 4.99% of the Company’s outstanding common stock, subject to increase to 9.99% upon 61 days’ prior written notice by the holder.

 

 

 

Pursuant to the SPA, the Company entered into a Registration Rights Agreement dated November 18, 2021, by and between the Company and the Purchaser, in which the Company has agreed to file a Registration Statement on Form S-1 with the SEC following request by the Purchaser at any time following the 180-day period after the initial closing.

 

The Company calculated the fair value of the Warrants using the Black Scholes method as $877,261 and recorded their fair value along with the $100,000 original issue discount and relates issuance costs of $20,249 as a debt discount which will be amortized using the straight-line method over the one year note period. Amortization of the debt discount for the year ended December 31, 2021 amounted to $117,515. The loan balance, net of discount was $220,005 as of December 31, 2021.

 

On March 3, 2022, the Company entered into an Exchange Agreement (the “Agreement”) with an institutional investor (the “Investor”) pursuant to which the Company agreed to issue a 10% original issue discount senior convertible promissory note in the principal amount of $385,000 (the “Second Note”) and five-year warrants to purchase 275,000 shares of the Company’s common stock, par value $0.0001 per share at an exercise price of $1.40 per share (the “Warrants”) in exchange for 350 shares of the Company’s Series A Convertible Preferred Stock (“Series A”). The Second Note matures on March 3, 2023. The Agreement was entered into after the Investor exercised the most favored nations rights contained in Section 7(b) of the Company’s Certificate of Designation of Preferences, Rights and Limitations of the Series A in connection with the consummation of a private placement with the Purchaser on November 18, 2021. The warrant fair value of $190,638 and the original issue discount of $35,000 were treated as a discount to the Second Note and will be amortized over the term of the Second Note. Amortization of the debt discount for the three months ended March 31, 2022, was $17,309 and was recorded as interest expense. The debt discount balance at March 31, 2022, was $208,283.

 

 

18

 

 

Paycheck Protection Program Funding U.S. Small Business Administration Loan

 

On May 28, 2020 , the Company received a secured, 30-year, Economic Injury Disaster Loan in the amount of $99,100 from the U.S. Small Business Administration. The loan carries interest at a rate of 3.75% per year, requires monthly payments of principal and interest, and matures in 30 years. Installment payments, including principal and interest, of $483 monthly, will begin 12 months from the date of the promissory Note. The SBA loan is secured by a security interest in the Company’s tangible and intangible assets. The loan proceeds are to be used as working capital to alleviate economic injury caused by the Covid-19 disaster occurring in the month of January 31, 2020 and continuing thereafter. As of March 31, 2022 the current principal balance of this note amounted to $99,100 and accrued interest was approximately $2,047.

 

Regarding Panacea Life Sciences, Inc.’s (PLS) Small Business Administration (SBA) loans, PLS received the PPP first draw loan in the amount of $273,300.00 on April 29, 2020. All funds were used to cover payroll expenses. The first draw loan, including any accrued interest, was officially forgiven by the SBA and the respective lending bank, FirstBank, on March 3, 2021. On January 28, 2021, PLS received the PPP second draw loan in the amount of $243,041.00; the second draw loan was forgiven on June 28, 2021.

 

PLS’s accounting treatment of the PPP loans and forgiveness follows best practice from the AICPA and accounted for the loan as a financial liability in accordance with FASB ASC 470 and accrue interest in accordance with the interest method under FASB ASC 835-30.

 

The aforementioned forgiveness of the first draw loan was recorded in the Company’s consolidated statement of operations as gain on extinguishment of debt.

 

Employer Retention Credit

 

The Company received an employer retention credit from the federal government of $253,791 in 2021.

 

Notes payable – related party and other liability

 

As part of the Exchange Agreement certain loan balances (“Quintel Loans”) from Quintel-MC Incorporated, an affiliate of the Company’s CEO, (“Quintel”) and historical interest owed of $1,932,358 were combined into a new promissory note with the principal amount of $4.062 million (“Quintel Note”). The Quintel Note bears annual interest at 12% and was secured by a pledge of certain XXII common stock owned by Panacea (See Note 2 Going concern).

 

On June 30, 2021, the Company issued its CEO, Ms. Buttorff, a 10% promissory note in the amount of $1,624,000 (the “Buttorff Note”). The Buttorff Note was secured by a pledge of certain XXII common stock owned by the Company (See Note 2 Going concern). This demand note replaced a prior working capital note that the Company had issued on January 1, 2021. On July 1, 2021, the Company issued Ms. Buttorff a 10%, $million line of credit note at 10% annual rate which Ms. Buttorff has increased that expired in January 2022, which Ms. Buttorff has extended (see Note 6 – Notes Payable – Buttorff Note). In January, 2022, the Buttorff line of credit was increased to $1.5 million and is now due on January 31, 2023. To date the balance due is $1,175,459.

 

On June 30, 2021 the $7 million of convertible debt (“XXII Debt”) was retired in exchange for a portion of the Needle Rock Farm ($2.2 million), $500,000 was converted to common stock and J&N Real Estate Company assumed a $4.3 million loan.

 

 

19

 

 

During October 2019, the Company issued a short-term promissory note to an officer of Exactus, for an aggregate principal amount of $55,556The note originally became due and payable between October 18, 2019 and December 16, 2019 and bore interest at a rate of twelve 12% per annum prior to the maturity date, and 18% per annum if unpaid following the maturity date. The current interest rate is 18%. The note is an unsecured obligation of the Company. The note carry a 10% original issue discount of $5,556 which has been amortized and recorded in interest expense on the accompanying consolidated statements of operations. As of December 31, 2021, the principal balance under this note was paid off.

 

 

 

March 31, 2022 December 31, 2021
Quintel Note $ 4,062,713 $ 4,062,713
CEO Note 2,861,144 2,379,153
Total related party notes $ 6,923,857 $ 6,441,866

Other long-term liabilities, related party

 

The Company has recorded a related party liability (“Fixed Asset Loan”) in the amounts of $2,899,919 and $2,749,638 as of March 31, 2022 and December 31, 2021, respectively, relating to SAP software and support fees which were paid by an affiliate company of the CEO. The balance bears interest of 6% and the maturity date has not yet been determined.

 

In 2020, the Company recorded an additional related party liability in the amount of $513,390 in respect to certain building improvements, due to J&N Real Estate Company (a company owned by the CEO) (“J&N Building Loan”). This balance bears no interest, and the maturity date has not yet been determined.

 

 

March 31, 2022 December 31, 2021
Other long-term liabilities, related party
Fixed Asset Loan $ 2,899,919 $ 2,749,638
J&N Building Loan 513,390 513,390
Total $ 3,413,309 $ 3,263,028

 

NOTE 7 – STOCKHOLDERS’ EQUITY

 

Common stock

 

The Company’s authorized common stock consists of 650,000,000 shares with a par value of $0.0001 per share.

 

During the three months ended March 31, 2022, the Company issued 679,694 shares of common stock in respect of the share exchange effected in 2021. In addition, 8,940 shares of common stock were issued to a service provider for a platform license for the year ended December 31, 2022.

 

 

20

 

 

Common stock options

 

Stock Option Plan

 

On June 30, 2021 the Company’s stockholders approved the 2021 Equity Incentive Plan (the “2021 Plan”). The 2021 Plan provided for the issuance of 4,049,409 incentive awards in the form of non-qualified and incentive stock options, restricted stock awards, restricted stock unit awards, warrants and preferred stock. The awards may be granted by the Company’s Board of Directors to its employees, directors and officers and to consultants, agents, advisors and independent contractors who provide services to the Company or to a subsidiary of the Company. The exercise price for stock options must not be less than the fair market value of the underlying shares on the date of grant. The incentive awards shall either be fully vested and exercisable from the date of grant or shall vest and become exercisable in such installments as the Board of Directors or Compensation Committee may specify. Stock options expire no later than ten years from the date of grant. Unless sooner terminated, the Plan shall terminate in 10 years.

 

Previously the Company had adopted the 2018 Equity Incentive Plan (the “2018 Plan”). The 2018 Plan provides for the issuance of incentive awards in the form of non-qualified and incentive stock options, stock appreciation rights, restricted stock awards, and restricted stock unit awards. The awards may be granted by the Company’s Board of Directors to its employees, directors and officers and to consultants, agents, advisors and independent contractors who provide services to the Company or to a subsidiary of the Company. The exercise price for stock options must not be less than the fair market value of the underlying shares on the date of grant. The incentive awards shall either be fully vested and exercisable from the date of grant or shall vest and become exercisable in such installments as the Board or Compensation Committee may specify. Stock options expire no later than ten years from the date of grant. The aggregate number of shares of common stock which may be issued pursuant to the Plan is 4,049,409 unless sooner terminated, the Plan shall terminate in 10 years. This plan had 196,491 fully vested options outstanding at the time of the share exchange. There have been no options granted under this plan subsequent to the share exchange.

 

Stock Options

 

A summary of the stock option activity is presented below:

 

Options Outstanding as of March 31, 2022
 

Number of

Shares Subject

to Options

Weighted

Average

Exercise

Price Per

Share

Weighted

Average

Remaining

Contractual

Life (in years)

Aggregate
Intrinsic
Value
Balance on December 31, 2021 196,491 $ 3.51 3.20 $
Options granted
Options exercised
Options canceled / expired
Balance at March 31, 2022 196,491 $ 3.51 2.95 $
Vested and exercisable at March 31, 2022 196,491 $ 3.51 2.95 $

Stock Warrants

 

On March 3, 2022, the Company entered in an Exchange Agreement with an institutional investor pursuant to which the Company issued a 10% original issue discount senior convertible promissory note in the principal amount of $385,000 (the “Note”) and five-year warrants to purchase 275,000 shares of the Company’s common stock, par value $0.0001 per share at an exercise price of $1.40 per share in exchange for 350 shares of the Company’s Series A Convertible Preferred Stock.

 

 

21

 

 

As of March 31, 2022, the Company also had outstanding warrants to purchase an aggregate of 56,377 shares of common stock. These warrants were previously issued by the Company prior to the exchange agreement.

 

The Company’s outstanding warrants as of March 31, 2022 are summarized as follows, and all were exercisable at that date.

 

Warrants Outstanding as of March 31, 2022
 

Number of

Shares Subject

to Warrants

Weighted

Average

Exercise

Price Per

Share

Weighted

Average

Remaining

Contractual

Life (in years)

Aggregate
Intrinsic
Value
Balance on December 31, 2021 56,377 $ 13.64 2.01
Options granted 275,000
Options exercised
Options canceled / expired
Balance at March 31, 2022 331,377 $ 3.48 4.39 $
Vested and exercisable at March 31, 2022 331,377 $ 3.48 4.39 $

As of March 31, 2022, the outstanding warrants have no intrinsic value.

 

Restricted Stock

 

A summary of the restricted stock activity is presented below:

 

Restricted Stock Common Stock
Balance at December 31, 2021 107,993
Balance at March 31, 2022 107,993

As of March 31, 2022, there were no unamortized or unvested stock-based compensation costs related to restricted share arrangements.

 

Preferred Stock

 

The Company’s authorized preferred stock consists of 50,000,000 shares with a par value of $0.0001.

 

On March 3, 2022, the Company entered into an Exchange Agreement with the Investor pursuant to which the company agreed to issue the Note in the principal amount of $385,000 and the Warrants in exchange for 350 shares of the Company’s Series A Convertible Preferred Stock. On April 19, 2022, the Company filed a Withdrawal of Designation of the Series A Convertible Preferred Stock with the Secretary of State and the State of Nevada.

 

 

22

 

 

NOTE 8 – COMMITMENTS AND CONTINGENCIES

 

Legal Matters

 

In the ordinary course of business, the Company enters into agreements with third parties that include indemnification provisions which, in its judgment, are normal and customary for companies in the Company’s industry sector. These agreements are typically with business partners, and suppliers. Pursuant to these agreements, the Company generally agrees to indemnify, hold harmless, and reimburse indemnified parties for losses suffered or incurred by the indemnified parties with respect to the Company’s products, use of such products, or other actions taken or omitted by us. The maximum potential number of future payments the Company could be required to make under these indemnification provisions is unlimited. The Company has not incurred material costs to defend lawsuits or settle claims related to these indemnification provisions. As a result, the estimated fair value of liabilities relating to these provisions is minimal. Accordingly, the Company has no liabilities recorded for these provisions as of March 31, 2022.

 

 

 

Concentrations

 

The Company has no contingencies, material commitments, or purchase obligations or sales obligations.

 

On the revenue side, in the three months ended March 31, 2022, we have a concentration of two customers. One is a customer who purchased PPE items and represents 22% of revenue. The other is a tolling partner who represents 17% of revenue. In the three months ended March 31, 2021, there was one customer who represented 25% of revenue and another that represented 11% of revenue.

 

The other concentration is in the accounts receivable category, where three customer accounts for 66% of the accounts receivable. One of the three customer contracts is unique in that we produced all of the products for them to sell, and they pay Panacea as the items are sold in the ecommerce marketplace. Thus, until their inventory is depleted, we will have accounts receivable. This customer receivable is 45% of the 66%.

 

NOTE 9 – RELATED PARTY TRANSACTIONS

 

Notes Payable and Accrued Interest – Related Parties

 

 

 

For information on related party loans to the Company and other related party transactions, see Notes 5 and 6, Operating Lease and Notes Payable.

 

 

23

 

 

The accrued interest and interest expenses recorded for related party loans are shown below.

 

March 31, 2022 December 31, 2021
Accrued Interest
Related party loan-Quintel $ 380,616 $ 249,939
Related party loan-CEO loan 130,724 86,060
Related party loan – Line of credit 59,370 29,235

 

Three months ended
March 31, 2022
Three months ended

March 31, 2021

Interest Expense
Related party loan-Quintel $ 130,678 $ 280,539
Related party loan-CEO loan 29,652 18,736
Related party loan – Line of Credit 30,135

Other

 

The Company continues to hold 1,227,017 shares of XXII stock which is available for sale. On August 25, 2021 70,000 shares were sold and the proceeds from the sale was $230,296. XXII recently moved from the NYSE to NASDAQ. As of March 31, 2022 XXII is a common shareholder of the Company.

 

NOTE 11– SUBSEQUENT EVENTS

 

On April 19, 2022, the Company filed a Withdrawal of Designation of the Series A with the Secretary of State and the State of Nevada.

 

In the second quarter we established a Scientific Advisory Board (“SAB”) consisting of seven members. These members were provided restricted stock. Since the legalization of industrial hemp extracts through the 2018 Agriculture Improvement Act, more commonly known as the Farm Bill, cannabinoids have exploded into the dietary supplement and food space. Marketers of cannabidiol (“CBD”), claim CBD products cure everything from arthritis to yeast infections with no substantial data to support such claims. Since its inception, the Company has committed to providing scientific and clinical data to better understand the impact of cannabinoids on human and animal health and to educate customers on how to use these products. Assembling a SAB consisting of experts in various scientific and medical specialties enhances the Company’s ability to design and evaluate clinical studies as well as provide guidance on product development. The SAB will be a critical element in assisting the Company to develop products with purpose. Currently, the Company has launched two analytical chemistry projects focused on isolation of minor cannabinoids and pesticide remediation, clinical animal studies to evaluate analgesia in dairy cattle and evaluation of CBD in canine age-related dementia. The latter is a translational model to understand the potential of CBD in slowing down or regressing Alzheimer’s Disease. The SAB has also reviewed human clinical studies to measure bioavailability of a variety of the Company’s products, CBD and Cannabigerol (“CBG”) in anxiety, CBG effects to support the digestive system as a potential supplement for those with irritable bowel syndrome and is collaborating with CU Anschutz on CBD and CBG effects in female patients diagnosed with chronic pelvic pain.

 

24

 

 

ITEM 2. MANAGEMENT’S DISCUSSION AND ANALYSIS OF FINANCIAL CONDITION AND RESULTS OF OPERATIONS.

 

Business Overview

 

The Company is a Nevada corporation organized in 2008. The Company has pursued opportunities in Cannabidiol, which we refer to as “CBD”, since December 2018 when we expanded our focus to pursue opportunities in hemp-derived CBD. Effective October 25, 2021, we changed our name to Panacea Life Sciences Holdings, Inc. To that end, on June 30, 2021 we entered into the Exchange Agreement with Panacea and the Panacea stockholders and as a result became a seed-to-sale CBD company. The former Panacea stockholders have assumed majority control of the Company, and all our operations are now operated through Panacea which because of the share exchange became a wholly-owned subsidiary of the Company. Leslie Buttorff, who became the Company’s Chief Executive Officer and a director upon the closing of the share exchange, also became our principal stockholder through common stock and Convertible Preferred Stock issued to her and entities she controls.

 

Panacea, the Company’s subsidiary after the share exchange, which was founded by Leslie Buttorff in 2017 as a woman-owned business, attracted a $14 million investment from 22nd Century Group, Inc., or XXII, a plant biotechnology company which also has a focus on CBD products and technology, during 2019. XXII has retained a 15% stake in the Company following the share exchange. Through Panacea, we are dedicated to developing and producing the highest-quality, most medically relevant, legal, hemp-derived cannabinoid products for consumers and pets. Beginning at a farm Panacea has the option to own a parcel of the farm located at Needle Rock, Colorado and leases laboratory space within a 51,000 square foot, state-of-the-art, cGMP, extraction, manufacturing, testing and fulfillment center located in Golden, Colorado, Panacea operates in every segment of the CBD product value chain. From cultivation to finished goods, Panacea ensures its products with stringent testing protocols employed at every stage of the supply chain. Panacea endeavors to offer pure natural remedies within product lines for every aspect of life: PANA Health®, PANA Beauty®, PANA Sport®, PANA Pet®, PANA Pure® and PANA Life®

 

In the first quarter of 2022 we obtained additional registration on two more of our six brands and our mark, so we now have registered trademarks on all of our brands.

 

Currently Panacea sells over 60 different product SKUs of CBD and CBG products. In addition, we offer “white label” licensing to retail businesses and contract manufacturing services to smaller CBD companies and softgel manufacturing to nutraceutical companies.

 

We were also engaged by a third-party company to develop various formulations for pet products and human products.

 

We believe that our competitive advantages are derived from being vertically integrated that allows for extraction, enrichment and manufacturing under a cGMP quality environment: 1) Using pharmaceutical formulation methods to optimize the delivery of various hemp products, 2) Developing both full spectrum and THC-free products, 3) Hemp supply, and 4) utilize Good Manufacturing Practice to produce goods that are safe and quality products that deliver consistent dosing. The ability to produce both full spectrum products (those that contain <0.3%) and THC-free products allows us to optimize dosage and delivery to various human conditions. Removal of the THC from products is a difficult and expensive process, but we believe this is essential for specific patient populations; such as, athletes where testing positive for THC would lead to disqualification, first responders who would be terminated for testing positive for THC, and in animal products where even a small amount of THC can lead to toxicity and potential lethality. Industrial hemp extracts are found to have particular application as neuroprotectants, for example in limiting neurological damage and increasing speed of recovery with traumatic brain injury. The cannabinoids have also been reported to treat human disease conditions where currently multiple pharmacologicals are needed to address, e.g., Post Traumatic Stress Disorder (PTSD), or where there is no current cure such as Alzheimer’s, Parkinson’s Disease, and age-related dementia, to name a few.

 

Although numerous reports describe cannabis/hemp extract health benefits the industry lacks sufficient clinical data and quality control to provide patient benefit. We are combining human and pet clinical studies with Good Manufacturing Process manufacturing to generate a panel of products. Our products are formulated with delivery methods for health benefits including an intellectual property portfolio enabling development of topical creams, sublinguals, oral soft gel capsules, patches, and sprays. Our products are derived from organic practices industrial hemp grown in Colorado.

 

 

 

 

25

 

 

We believe a multitude (hundreds) of companies, large and small, have launched or intend to launch retail brands and white label products containing cannabinoids like CBD, including retail and seed-to-sale companies that are larger and better capitalized than we are and/or which offer products similar to ours with a larger geographic scope of operations and a market presence. Many of these are dependent upon third parties to provide raw material inventory for sale. We believe this makes many of the participants in the industry vulnerable to shortages, quality issues, reliability, and pricing variability. Our industry relationships may allow us to build an efficient supply chain that will put us among the few companies that maintain a competitive pricing and supply advantage. The CBD-based consumer product industry is highly fragmented with numerous companies. There are also large, well-funded companies that currently do not offer hemp-based consumer products including large agribusiness companies but may do so in the future and become significant competitors. Our goal is to be a leader in wholesale and retail sales channels for end-products, such as nutraceuticals, supplements and pet and farm products. As government regulation of CBD and related products becomes more lenient in certain jurisdictions, and other barriers to entry decline, we anticipate experiencing an increase in competition and an intensifying competitive environment, including potentially the introduction of new seed-to-sale companies and/or the expansion of operations by current competitors. Further, numerous other factors are expected to be critical to our ability to be and remain competitive in our business and goals, including product quality and prices, brand strength, production and distribution capabilities and geographic scope of operations and market presence. Additionally, market conditions can shift demand for CBD products, such as competitive pricing, the effects of inflation, regulatory changes and economic or geopolitical turmoil.

 

Our Industrial Hemp Supply

 

 

In 2019, Panacea acquired Needle Rock Farms (NRF) in Crawford, Colorado. Our 2020 hemp crop was grown at NeedleRock Farms. Also, in December, 2019 XXII made a $14 million investment in Panacea which consisted of $7 million in preferred stock and $7 million in convertible debt. XXII also was to provide an additional $10 million in funding at a later point in time. On June 30, 2021 Panacea and XXII agreed to dissolve the agreement and agreed on the following: the preferred stock was converted to common stock; a $4.3 million loan was secured against the laboratory space owned by J&N Real Estate, LLC (owned by Panacea’s CEO), the NRF and equipment would be transferred to XXII in exchange for a reduction of $2.2 million in convertible debt, 10 acres of the farm would be sub platted to Panacea, $500,000 in hemp would be delivered from the 2021 crop yield, and a 15-year agreement for hemp supply would be finalized after the deal was completed. In 2021 XXII was the grower at NRF and achieved USDA Organic certification for the farm. As of the date of this Report, XXII has not delivered the $500,000 of hemp to Panacea, nor have we closed on the 10 acres. However, we also have the 2020 NRF crop and several hemp tolling contracts in which the output of crude and or distillate is shared with the growers to process.

 

Partnership with Universities

 

The grand opening of the Panacea Life Sciences Cannabinoid Research Center at Colorado State University was held on October 19, 2021. The first studies at the center are underway for isolation of rare cannabinoids, examining cannabidiol’s effects on Inflammatory Bowel Disease (IBS), canine and human dementia, as well as supporting research into chronic pelvic pain. We have also signed an agreement with the Colorado School of Mines in the area of developing hemp-based sustainability products.

 

Company Information Technology Infrastructure

 

The ERPCannabis system is based on an SAP architecture and was used to develop the base installation. All financial, human resource, payroll, procurement, production planning and materials management business processes are represented in this system. In addition, the system is linked to our e-Commerce website www.panacealife.com. This system allows us to update product costing and determine inventory levels which will be critical as the company expands. In addition, sophisticated financial and payroll processing are inherent in the solution; thus, offering investors detailed accounting results related to company investments. We plan to expand on the use of this infrastructure for acquisitions and service offerings.

 

Results of Operations

 

Set forth below is the discussion of the results of operations of the Company for the three months ended March 31, 2022 compared to the three months ended March 31, 2021. The information which follows relates to the operations of Panacea which under applicable accounting rules are treated as the operation of the Company.

 

 

 

 

26

 

 

Three Months Ended March 31, 2022 and 2021

 

Net Revenues

 

We are principally engaged in the business of producing and selling products made from industrial hemp. Revenue consists of sales of our six category of brand products, white label and contract manufacturing sales to other CBD companies, raw material sales (distillate and isolate), tolling products, and leasing space. We also have revenue from the sale of our Personal Protection Equipment (PPE) inventory and non-CBD nutraceutical companies.

 

Our revenues for the three months ended March 31, 2022, decreased by $45,664, or 9%, to $466,474 as compared to $512,138 for the three months ended March 31, 2021. The decrease in sales in 2022 was due primarily to fewer white label customers.

 

Cost of Sales

 

Cost of sales for the three months ended March 31, 2022, increased by $36,254 or 11% to $366,091 as compared to $329,837 for the three months ended March 31, 2021. The increase in cost of sales was due primarily to increased raw material costs. The primary components of cost of sales include the cost of manufacturing the CBD products.

 

Operating Expenses

 

Operating expenses for the three months ended March 31, 2022, increased by $474,390, or 37%, to $1,748,367 as compared to $1,273,977 for the three months ended March 31, 2021. This is due to increases in both operating expenses and general and administrative expenses.

 

 

Operating expenses for the three months ended March 31, 2022, increased by $299,882, or 30%, to $1.288 million as compared to $0.988 million during the three months ended March 31, 2021. The increase in production related operating expenses is primarily due to increased salary and labor costs and increased storage costs.

 

General and administrative expenses for the three months ended March 31, 2022, increased by $174,508, or 59%, to $0.456 million as compared to $0.286 million during the three months ended March 31, 2021. The increase in general and administrative costs is primarily due to increased legal and audit costs as part of becoming a publicly traded company as well as a one-time fee paid for entrance into the Brazil market.

 

Other income (expense)

 

Other income for the three months ended March 31, 2022, decreased by $2,596,589 or 178% to ($1,134,262) as compared to 1,462,326 for the three months ended March 31, 2021. The decrease in other income is primarily due to the unrealized loss of marketable securities held.

 

 

Liquidity and Capital Resources

 

Cash flows from operating activities

 

The largest source of operating cash is from our customers. A large majority of our customers purchase CBD on-line, so credit card payments are collected and paid within 1-2 business days. Other white label and contract manufacturing customers pay before the products are released. Some larger customers have either net 10-, 2%- or 30-day net terms. Net cash used in operating activities was $436,043 and $795,228 for three months ended March 31 for 2022 and 2021, respectively. Approximately $2.1 million of our $2.8 million net loss in 2022 was non-cash.

 

Cash flows from investing activities

 

Cash outlay for the acquisition of fixed assets comprised the majority of this category and were $0.010 million and $0.087 million for the three months ended March 31, 2022 and 2021, respectively.

 

 

 

 

27

 

 

Cash flows from financing activities

 

Net cash provided by financing activities for the three months ended March 31, 2022 was $0.482 million. For the same period in 2021 the financing was $0.895 million. In both years the primary financing was cash provided by Company’s CEO. In 2021, there was a cash payment received of $0.243 from the paycheck loan program.

 

 

On March 31, 2022, we had $2.903 million in cash and liquid stock of XXII. The Chief Executive Officer of the Company holds the XXII shares pursuant to the pledge agreement and has the power at any time to permit the Company to sell the shares to provide working capital. In August 2021, 70,000 shares were sold for working capital. Panacea has borrowed substantial sums from Leslie Buttorff, our Chief Executive Officer, to meet its working capital obligations. On March 31, 2022 Panacea issued an affiliate of Ms. Buttorff a 12% demand promissory note for $4.063 million and issued Ms. Buttorff a 10% demand promissory note for $1.624 million secured by a pledge of certain XXII common stock owned by Panacea. On July 1, 2021, the Company issued Ms. Buttorff a $1 million line of credit note at 10% annual rate which Ms. Buttorff has increased that expired in January 2022, which Ms. Buttorff has extended to January, 2023 and increased the line of credit to $1.5 million.

 

We do not have sufficient cash resources to sustain our operations for the next 12 months, particularly if the large sales agreements and purchase orders we have do not result in the revenue anticipated. We may be dependent on obtaining financing from one or more debt or equity offerings or further loans from Ms. Buttorff assuming she agrees to advance further funds.

 

These unaudited condensed consolidated financial statements are presented on the basis that the Company will continue as a going concern. The going concern concept contemplates the realization of assets and satisfaction of liabilities in the normal course of business. No adjustment has been made to the carrying amount and classification of the Company’s assets and the carrying amount of its liabilities based on the going concern uncertainty. These factors raise substantial doubt about the Company’s ability to continue as a going concern for a period of 12 months from the issuance date of this report. Management cannot provide assurance that the Company will ultimately achieve profitable operations or become cash flow positive or raise additional debt and/or equity capital. In addition, due to insufficient revenue, we will need to obtain further funding through public or private equity offerings, debt financing, collaboration arrangements or other sources in order to maintain active business operations. We currently do not have sufficient cash flow to pay our ongoing financial obligations on a consistent basis. The issuance of any additional shares of common stock, preferred stock or convertible securities could be substantially dilutive to our stockholders. In addition, adequate additional funding may not be available to us on acceptable terms, or at all. If we are unable to raise capital, we will be forced to borrow additional sums from our Chief Executive Officer or delay, reduce or eliminate our research and development programs, we may not be able to continue as a going concern, and we may be forced to discontinue operations. These unaudited condensed consolidated financial statements do not include any adjustments related to the recoverability and classification of assets or the amounts and classification of liabilities that might be necessary should the Company be unable to continue as a going concern.

 

Off Balance Sheet Arrangements

 

As of March 31, 2022, we had no material off-balance sheet arrangements.

 

 

 

 

28

 

 

Potential Impacts of the COVID-19 Pandemic on Our Business Operations

 

As disclosed in Note 2, the COVID-19 pandemic has had a notable impact on general economic conditions, including but not limited to the temporary closures of many businesses, “shelter in place” and other governmental regulations, reduced business and consumer spending due to both job losses and reduced investing activity, among many other effects attributable to the COVID-19 pandemic. Presently we do not know whether future variants will have an adverse effect on our operations.

 

Various variants may extend throughout 2023.

 

Potential Impacts of Certain Current and Proposed Regulations on Our Business and Operations

 

Recently, a bill titled the Cannabis Administration and Opportunity Act, put forward by Senate Majority leader Chuck Schumer, D-NY, would amend the definition of a dietary supplement to remove the prohibition on marketing CBD as a dietary supplement. Management sees the bill, if enacted, as an opportunity for the FDA to accelerate their decision to classify CBD products as a dietary supplement. This would be a significant step for hemp/CBD companies as it would open the door to new selling opportunities, such as getting into retail stores, who have largely been hesitant to welcome CBD in their doors without a clear position from the FDA.

 

Many people are increasingly turning to CBD products for several reasons: CBD is non-psychoactive, so it does not produce a “high” like THC, there are few known contraindications, the properties of different cannabinoids can positively affect a wide range of ailments, and cannabinoids work directly and indirectly with the body’s endocannabinoid system to create balance known as homeostasis. As demand increases, we believe the FDA must provide more clarity about CBD’s legalization, and this bill is a promising first step.

 

For now, many companies that produce hemp-derived CBD products including Panacea undertake to abide by the same regulations as any other dietary supplements like ingredient filings, good manufacturing practices (GMP), and labeling and marketing provisions. Panacea will continue to sell CBD and other hemp-derived products while still awaiting a clear path from the FDA about how CBD products can be marketed and used.

 

Cautionary Statement Regarding Forward-Looking Statements

 

This quarterly report on Form 10-Q (this “Report”) contains forward-looking statements within the meaning of the Private Securities Litigation Reform Act of 1995, including statements about our new operations in the hemp industry through Panacea, our expected revenue growth, our human resources following our recent acquisition of Panacea, proposed federal legislation and its potential impact on the CBD industry, our business relationship with XXII, our plans to raise capital, and our liquidity. Words such as “expects,” “anticipates,” “plans,” “believes,” “seeks,” “estimates,” “could,” “would,” “may,” “intends,” “targets” and similar expressions or variations of such words are intended to identify forward-looking statements but are not the exclusive means of identifying forward-looking statements in this Report. The identification of certain statements as “forward-looking” is not intended to mean that other statements not specifically identified are not forward-looking. All statements other than statements about historical facts are statements that could be deemed forward-looking statements, including, but not limited to, statements that relate to our future revenue, product development, customer demand, market acceptance, growth rate, competitiveness, gross margins, and expenditures.

 

Although forward-looking statements in this Report reflect the good faith judgment of our management, such statements can only be based on facts and factors currently known by us. Further information on the risks and uncertainties affecting our business is contained in our filings with the SEC, including this Form 10-Q and our Annual Report on Form 10-K for the fiscal year ended December 31, 2021. We undertake no obligation to publicly update or revise any forward-looking statements, whether as the result of new information, future events or otherwise. Such risks, uncertainties and changes in condition, significance, value, and effect could cause our actual results to differ materially from those expressed herein and in ways not readily foreseeable. Readers are urged not to place undue reliance on these forward-looking statements, which speak only as of the date of this Report and are based on information currently and reasonably known to us. We undertake no obligation to revise or update any forward-looking statements to reflect any event or circumstance that may arise after the date of this Report, other than as required by law. Readers are urged to carefully review and consider the various disclosures made in this Report, which attempt to advise interested parties of the risks and factors that may affect our business, financial condition, results of operations and prospects.

 

 

29

 

 

Critical Accounting Estimates and New Accounting Pronouncements

 

New Accounting Pronouncements

 

See Note 2, SUMMARY OF SIGNIFICANT ACCOUNTING POLICIES to the unaudited condensed consolidated financial statements contained in Part I, Item 1 of this amendment No. 1 to the Quarterly Report on Form 10-Q.

 

Critical Accounting Estimates

 

The discussion and analysis of the Company’s financial condition and results of operations is based upon the Company’s condensed consolidated financial statements, which have been prepared in accordance with US GAAP. The preparation of the Company’s condensed consolidated financial statements requires its management to make estimates and judgments that affect the reported amounts of assets, liabilities, revenue and expenses and related disclosures. The Company’s management bases its estimates, assumptions and judgments on historical experience and various other factors that are believed to be reasonable under the circumstances, the results of which form the basis for making judgments about the carrying values of assets and liabilities that are not readily apparent from other sources. Different assumptions and judgments would change the estimates used in the preparation of the Company’s condensed consolidated financial statements which, in turn, could change the results from those reported. In addition, actual results may differ from these estimates and such differences could be material to the Company’s financial position and results of operations.

 

Critical accounting estimates are those that the Company’s management considers the most important to the portrayal of the Company’s financial condition and results of operations because they require management’s most difficult, subjective or complex judgments, often as a result of the need to make estimates about the effect of matters that are inherently uncertain. The Company’s critical accounting estimates in relation to its condensed consolidated financial statements include those related to:

 

Goodwill and intangible assets
Fair value of marketable securities
Incremental Borrowing Rate used Right of Use Asset Calculations
Business combinations

 

Goodwill and Indefinite-Lived Intangibles

 

We allocate the cost of acquired companies to the identifiable tangible and intangible assets acquired and liabilities assumed, with the remaining amount classified as goodwill. The identification and valuation of these intangible assets and the determination of the estimated useful lives at the time of acquisition, as well as the completion of impairment tests, require significant management judgments and estimates. These estimates are made based on, among other factors, review of projected future operating results and business plans, economic projections, anticipated highest and best use of future cash flows and the cost of capital. The use of alternative estimates and assumptions could increase or decrease the estimated fair value of goodwill and other intangible assets, and potentially result in a different impact to our results of operations. Further, changes in business strategy and/or market conditions may significantly impact these judgments and thereby impact the fair value of these assets, which could result in an impairment of the goodwill or intangible assets.

 

Goodwill is not amortized but is tested for impairment annually and whenever events or circumstances change that indicate impairment may have occurred. We tested goodwill for impairment and determined there was no impairment and found not impairment charge based on the excess of a reporting unit’s carrying amount over our fair value.

 

Fair value of marketable securities

 

Marketable securities are recorded at fair value using the quoted market prices and changes in fair value are recorded as net realized gains or losses in comprehensive income. We monitor these investments for impairment and make appropriate reductions in carrying values as necessary.

 

Incremental Borrowing Rate used Right of Use Asset Calculations

 

We determine if a contract is a lease or contains a lease at the inception of the contract and reassess that conclusion if the contract is modified. All leases are assessed for classification as an operating lease or a finance lease. Operating lease right-of-use, or ROU, assets are included in non-current other assets on our consolidated balance sheet. Operating lease liabilities are separated into a current portion, included within other accrued liabilities on our consolidated balance sheet, and a non-current portion, included within other long-term liabilities on our consolidated balance sheet. We do not have any finance lease ROU assets or liabilities. ROU assets represent our right to use an underlying asset for the lease term and lease liabilities represent our obligation to make lease payments arising from the lease. We do not obtain and control the right to use the identified asset until the lease commencement date.

 

 

 

 

 

 

30

 

 

Our lease liabilities are recognized at the applicable lease commencement date based on the present value of the lease payments required to be paid over the lease term. Because the interest rate implicit in the lease is not readily determinable, we generally use our incremental borrowing rate to discount the lease payments to present value. The estimated incremental borrowing rate is derived from information available at the lease commencement date. We factor in publicly available data for instruments with similar characteristics when calculating our incremental borrowing rates. Our ROU assets are also recognized at the applicable lease commencement date. The ROU asset equals the carrying amount of the related lease liability, adjusted for any lease payments made prior to lease commencement and lease incentives provided by the lessor. Variable lease payments are expensed as incurred and do not factor into the measurement of the applicable ROU asset or lease liability.

 

Business Combinations

 

We have applied significant estimates and judgments in order to determine the fair value of the identified assets acquired, liabilities assumed and goodwill recognized in connection with our business combinations to ensure the value of the assets and liabilities acquired are recognized at fair value as of the acquisition date. In measuring the fair value, we utilize valuation techniques consistent with the market approach, income approach, or cost approach.

 

The valuation of the identifiable assets and liabilities includes assumptions made in performing the valuation, such as projected revenue, weighted average cost of capital, discount rates, estimated useful lives, and other relevant assessments. These assessments can be significantly affected by our estimates, judgments, and assumptions. If actual results are not consistent with our estimates, judgments, or assumptions, or if additional or new information arises in the future that affects our fair value estimates, then adjustments to our initial fair value estimates may have a material impact to our purchase accounting or our results of operations. If actual results are not consistent with our estimates, judgments, or assumptions, or if additional or new information arises in the future, beyond our one-year measurement period, that affects our fair value estimates, then adjustments to our initial fair value estimates may have a material impact to our results of operations.

 

ITEM 3. QUANTITATIVE AND QUALITATIVE DISCLOSURES ABOUT MARKET RISK.

 

A smaller reporting company is not required to provide the information required by this Item.

 

ITEM 4. CONTROLS AND PROCEDURES.

 

 

Evaluation of Disclosure Controls and Procedures

 

Our management carried out an evaluation, with the participation of our Principal Executive Officer (who also now serves as our Principal Financial Officer), required by Rule 13a-15 or 15d-15 of the Securities Exchange Act of 1934 (the “Exchange Act”) of the effectiveness of our disclosure controls and procedures as defined in Rule 13a-15(e) or 15d-15(e) under the Exchange Act. Based on their evaluation, our Principal Executive Officer (who also now serves as our Principal Financial Officer) concluded that our disclosure controls and procedures are effective as of the end of the period covered by this report to ensure that information required to be disclosed by us in the reports that we file or submit under the Exchange Act is recorded, processed, summarized and reported within the time periods specified in the SEC’s rules and forms and is accumulated and communicated to our management, including our Principal Executive Officer and Principal Financial Officer, as appropriate to allow timely decisions regarding required disclosure.

 

Changes in Internal Control Over Financial Reporting

 

 

For the year-ended December 31, 2021, our Principal Executive Officer (who also now serves as our Principal Financial Officer) concluded that our disclosure controls and procedures were ineffective as of the end of that period. Since then, the Company has implemented three primary types of accounting controls that fall into categories of detection, preventive and corrective controls. These allow us to maintain effective controls for our financial reports. Using our ERP SAP system many accounting controls are already configured such as segregation of duties, independent user IDs and passwords and bank reconciliations. Other trial balance checks are completed within the system. In addition, monthly inventory and asset reconciliations are completed. Standard Operating Procedures are used throughout the organization, not only in the financial areas, but in all areas to maintain our GMP certifications for manufacturing. As a result, we believe that we have remediated the underlying issues.

 

Except as noted above, there were no changes in our internal control over financial reporting as defined in Rule 13a-15(f) or 15d-15(f) under the Exchange Act that occurred during the period covered by this report that have materially affected, or are reasonably likely to materially affect, our internal control over financial reporting.

 

 

 

 

 

31

 

 

PART II—OTHER INFORMATION

 

ITEM 1. LEGAL PROCEEDINGS.

 

From time–to-time, we may become involved in legal proceedings arising in the ordinary course of business. We are unable to predict the outcome of any such matters or the ultimate legal and financial liability, and at this time cannot reasonably estimate the possible loss or gain or range of loss/gain and accordingly have not accrued a related liability.

 

ITEM 1A. RISK FACTORS.

 

Not applicable.

 

ITEM 2. UNREGISTERED SALES OF EQUITY SECURITIES OR USE OF PROCEEDS.

 

During the three months ended March 31, 2022, the Company Issued 123,334 shares of the Company’s common stock to the former Chief Strategy Officer of the Company in connection with the cashless exercise of stock options, as well as 447 shares the Company owed the former Chief Strategy Officer for inadvertently issuing less shares of common stock than the amount indicated on the Subscription Agreement dated January 18, 2019. The issuance of the shares was exempt from registration pursuant to Section 4(a)(2) of the Securities Act of 1933 and Rule 506(b) promulgated thereunder.

 

 

ITEM 3. DEFAULTS UPON SENIOR SECURITIES.

 

None.

 

ITEM 4. MINE SAFETY DISCLOSURES.

 

Not applicable.

 

ITEM 5. OTHER INFORMATION.

 

None.

 

 

32

 

 

ITEM 6. EXHIBITS.

 

Incorporated by Reference Filed or Furnished
Exhibit # Exhibit Description Form Date Number Herewith
3.1 Amended Articles of Incorporation 8-K 7/7/21 3.1
3.1(a) Certificate of Amendment to its Amended and Restated Articles of Incorporation – name change and reverse stock split 8-K 10/29/21 3.1
3.2 Amended Bylaws 8-K 7/7/21 3.2
3.3 Certificate of Designation for Series A Preferred Stock 8-K 2/18/21 4.1
3.4 Certificate of Designation for Series B-1 Preferred Stock 8-K 3/4/16 3.1
3.5 Certificate of Designation for Series B-2 Preferred Stock 8-K/A 2/17/16 3.2
3.6 Certificate of Designation for Series C Preferred Stock 10-Q 8/23/21 3.7
3.7 Certificate of Designation for Series C-1 Preferred Stock 10-Q 8/23/21 3.8
3.8 Certificate of Designation for Series C-2 Preferred Stock 8-K 10/29/21 3.2
3.9 Certificate of Designation for Series D Preferred Stock 10-Q 8/23/21 3.9
3.10 Certificate of Withdrawal for Series A 10-K/A 4/29/22 3.10
10.1 Amended and Restated 2021 Equity Incentive Plan* 10-K 3/31/22 10.2
10.2 Form of Exchange Agreement** 8-K 3/4/22 10.1
10.3 Form of Original Issue Discount Senior Convertible Promissory Note 8-K 3/4/22 10.2
10.4 Form of Warrant 8-K 3/4/22 10.3
10.5 Form of Registration Rights Agreement** 8-K 3/4/22 10.4
31.1 Certification of Principal Executive Officer and Principal Financial Officer (302) Filed
32.1 Certification of Principal Executive and Principal Financial Officer (906) Furnished***
101.INS Inline XBRL Instance Document – the instance document does not appear in the Interactive Data File because its XBRL tags are embedded within the Inline XBRL document
101.SCH Inline XBRL Taxonomy Extension Schema Document Filed
101.CAL Inline XBRL Taxonomy Extension Calculation Linkbase Document Filed
101.DEF Inline XBRL Taxonomy Extension Definition Linkbase Document Filed
101.LAB Inline XBRL Taxonomy Extension Label Linkbase Document Filed
101.PRE Inline XBRL Taxonomy Extension Presentation Linkbase Document Filed
104 Cover Page Interactive Data File (formatted as Inline XBRL and contained in Exhibit 101)

 

* Management contract or compensatory plan or arrangement.

** Exhibits and/or Schedules have been omitted. The Company hereby agrees to furnish to the Securities and Exchange Commission upon request any omitted information.

*** This exhibit is being furnished rather than filed and shall not be deemed incorporated by reference into any filing, in accordance with Item 601 of Regulation S-K.

+Portions of this exhibit have been omitted as permitted by the rules of the SEC. The information excluded is both (i) not material and (ii) would be competitively harmful if publicly disclosed. The Company undertakes to submit a marked copy of this exhibit for review by the SEC Staff, to the extent it has not been previously provided, and provide supplemental materials to the SEC Staff promptly upon request.

 

Copies of this report (including the financial statements) and any of the exhibits referred to above will be furnished at no cost to our shareholders who make a written request to Panacea Life Sciences Holdings, Inc., at the address on the cover page of this report, Attention: Corporate Secretary.

 

 

33

 

 

SIGNATURES

 

Pursuant to the requirements of the Securities Exchange Act of 1934, the registrant has duly caused this report to be signed on its behalf by the undersigned thereunto duly authorized.

 

  Panacea Life Sciences Holdings, Inc.
   
May 13, 2022 /s/ Leslie Buttorff
Leslie Buttorff
Chief Executive Officer

 

SEC Filing

Panacea Life Sciences Adds Vegan Softgel Manufacturing Capabilities to Meet the Growing Demand for Clean, Natural Alternatives to Animal Derivatives

GOLDEN, CO / ACCESSWIRE / May 12, 2022 / Panacea Life Sciences, Inc. (OTCQB:PLSH), (“Panacea” or the “Company”), a Colorado, USA-based cannabinoid research and certified GMP manufacturing company is pleased to introduce their new vegan softgel manufacturing capabilities for Panacea CBD products and private label and nutraceutical partners.

Panacea Life Sciences, Inc, Wednesday, May 11, 2022, Press release picture

Using proprietary technology and two plus years of research and development, Panacea has successfully mass-produced vegan softgels. As an alternative to using bovine (an animal byproduct), vegan softgels are made from plant-based ingredients which provides a cleaner, more natural, and animal-free product. Panacea’s vegan softgel option is made from tapioca starch derived from the root of the cassava plant and is non-GMO Project verified. The capability of a vegan softgel option is an ideal way to expand a manufacturer’s product portfolio. In addition, the vegan softgel formulation provides superior stability which exceeds that of animal (bovine) gelatin and satisfies the vegetarian and vegan requirements of a large consumer base.

With two softgel lines that are able to produce over 1 million softgels per day (in a multitude of sizes), Panacea Life Sciences has proprietarily engineered equipment which manufactures vegan softgels more efficiently, and in turn, makes it more cost effective for clients. Compared to other delivery forms, vegan softgels have many favorable features:

“Panacea vegan softgels meet many clean label standards requested by Panacea customers and helps our contract manufacturing customers create product differentiation in the highly competitive CBD and Nutraceutical markets” comments Nick Cavarra, Panacea’s EVP of Sales and Marketing.

Panacea Life Sciences, Inc. will be attending the White Label World Expo in Las Vegas on May 25th and 26th. Find them at booth #5083 or visit panacealife.com for more information.

About Panacea Life Sciences Holdings, Inc.

Panacea Life Sciences Holdings, Inc. is a seed to sale cannabinoid manufacturer and research company that produces purposeful, natural medicine for consumers and pets. Panacea sells softgels, gummies, tinctures, sublingual tablets, cosmetics, and other topicals. If you would like more information about this topic or to learn more about Panacea and its products or our land-to-brand practices, please visit www.panacealife.com.

Cautionary Note Regarding Forward-Looking Statements

This press release contains forward-looking statements within the meaning of the Private Securities Litigation Reform Act of 1995, including statements regarding the effectiveness of CBD and other cannabinoids improving the lives of people and pets. You can identify forward-looking statements by use of the words “may,” “will,” “should,” “plans,” “explores,” “expects,” “anticipates,” “continue,” “estimate,” “project,” “intends,” and similar expressions. Forward-looking statements involve risks and uncertainties that could cause actual results to differ materially from those projected or anticipated. These risks and uncertainties include, but are not limited to, risks arising from supply chain disruptions on our ability to obtain raw materials as well as similar problems with our vendors, the impact of the pandemic including new variants on the national and global economy, the impact on the Russian invasion of Ukraine on the global economy, lack of available funding at sufficient levels to meet our working capital needs, competition from third parties; intellectual property rights of third parties; regulatory constraints, including the need for FDA approval under certain circumstances; and changes in technology and methods of marketing; as well as those risks and uncertainties described by us in our annual report on Form 10-K for the fiscal year ended December 31, 2021 under the heading “Risk Factors”. Any forward-looking statement made by us herein speaks only as of the date on which it is made. Factors or events that could cause our actual results to differ may emerge from time to time, and it is not possible for us to predict all of them. We undertake no obligation to publicly update any forward-looking statement, whether as a result of new information, future developments, or otherwise, except as may be required by law.

Contact:

Nick Cavarra
[email protected]

SOURCE: Panacea Life Sciences Holdings, Inc.

Panacea Life Sciences Current Report

 

UNITED STATES

SECURITIES AND EXCHANGE COMMISSION

Washington, DC 20549

 

Form 8-K

 

CURRENT REPORT

Pursuant to Section 13 or 15(d) of the Securities Exchange Act of 1934

 

Date of Report (Date of earliest event reported): May 3, 2022

 

PANACEA LIFE SCIENCES HOLDINGS, INC.

(Exact name of the registrant as specified in its charter)

 

Nevada 001-38190 27-1085858
(State or other jurisdiction of (Commission (IRS Employer
of incorporation) File Number) Identification No.)

 

5910 South University BlvdC18-193

Greenwood VillageCO 80121

 

(Address of principal executive offices) (Zip code)

 

Registrant’s telephone number, including area code: 1-800985-0515

 

Check the appropriate box below if the Form 8-K filing is intended to simultaneously satisfy the filing obligation of the Registrant under any of the following provisions (see General Instruction A.2 below):

 

Written communications pursuant to Rule 425 under the Securities Act (17 CFR 230.425).
Soliciting material pursuant to Rule 14a-12 under the Exchange Act (17 CFR 240.14a-12).
Pre-commencement communications pursuant to Rule 14d-2(b) under the Exchange Act (17 CFR 240.14d-2(b)).
Pre-commencement communications pursuant to Rule 13e-4(c) under the Exchange Act (17 CFR 240.13e-4(c)).

 

Securities registered pursuant to Section 12(b) of the Act:

 

Title of each class Trading symbol(s) Name of exchange on which registered
N/A N/A N/A

 

Indicate by check mark whether the registrant is an emerging growth company as defined in Rule 405 of the Securities Act of 1933 (§230.405 of this chapter) or Rule 12b-2 of the Securities Exchange Act of 1934 (§240.12b-2 of this chapter).

 

Emerging growth company 

 

If an emerging growth company, indicate by check mark if the registrant has elected not to use the extended transition period for complying with any new or revised financial accounting standards provided pursuant to Section 13(a) of the Exchange Act. ☐

 

 

 

 

 

Item 7.01. Regulation FD Disclosure.

 

On May 3, 2022, Ms. Leslie Buttorff, Chief Executive Officer of Panacea Life Sciences Holdings, Inc. made a presentation to certain members of the investment community. A copy of such presentation is being furnished herewith as Exhibit 99.1 to this report.

 

The information in this Item 7.01 of this report, including the information in the presentation attached as Exhibit 99.1 to this report, is furnished and shall not be deemed “filed” for the purposes of Section 18 of the Securities Exchange Act of 1934 (the “Exchange Act”) or otherwise subject to the liabilities of that section. Furthermore, the information in Item 7.01 of this report, including the information in the presentation attached as Exhibit 99.1 to this report, shall not be deemed to be incorporated by reference in the filings of the registrant under the Securities Act of 1933, or the Exchange Act.

 

Item 9.01 Financial Statements and Exhibits

 

(d) Exhibits.

 

Exhibit No. Exhibit
99.1 Investor Presentation
104 Cover Page Interactive Data File (embedded within the Inline XBRL document)

 

 

 

SIGNATURES

 

Pursuant to the requirements of the Securities Exchange Act of 1934, the registrant has duly caused this report to be signed on behalf of the undersigned hereunto duly authorized.

 

Panacea Life Sciences Holdings, Inc.
By: /s/ Leslie Buttorff
Date: May 3, 2022 Name: Leslie Buttorff
Title: Chief Executive Officer
SEC Filing

Panacea Life Sciences Holdings, Inc. Announces Participation in Investor Summit Group’s Q2 In-Person Conference

GOLDEN, CO / ACCESSWIRE / May 3, 2022 / Panacea Life Sciences Holdings, Inc. (OTCQB:PLSH) is pleased to announce that Leslie Buttorff will be in attendance at The Q2 Investor Summit Group – In-Person. Panacea Life Sciences Holdings’ Chief Executive Officer, Leslie Buttorff, will discuss the company’s roadmap for growth in the next 1-2 years.

Event: The Q2 Investor Summit Group
Date: May 3-4, 2022
Location: The Westin New York Grand Central
212 E 42nd St, New York, NY 10017
Presentation: May 3rd at 1:15PM ET
View webcast presentation: https://newsroom.panacealife.com

About Panacea Life Sciences Holdings, Inc.

Panacea Life Sciences Holdings, Inc. (OTCQB:PLSH) is a fully integrated FDA, cGMP certified, seed-to-sale cannabinoid product focused company. We research, develop, manufacture and commercialize raw materials derived from industrial hemp and custom formulate, manufacture and distribute softgels (both bovine and vegan), gummies, tinctures, sublingual tablets, patches, K-Tape, topical pain relief and skin care products as our base business. We have expanded our research and development preclinical and clinical programs, with a focus on nutraceutical and purposeful, natural pharmaceutical alternatives for humans and companion animals. We research, produce, and distribute products both domestically and internationally that target and treat major categories of medical conditions: pain, cancer, psychological, epilepsy, gastrointestinal, autoimmune, neurological, and sleep disorders and support these product through clinical research and studies. These categories include conditions that affect hundreds of millions of patients and animals worldwide.Our vision is to become the leading research and manufacturing cannabinoid and nutraceutical company (top 10 in terms of revenue and brand) in the U.S.

For further information:

Panacea Life Sciences Holdings, Inc.
Leslie Buttorff
3034340215
[email protected]

About the Investor Summit Group

The Investor Summit Group (formerly MicroCap Conference) is an exclusive, independent conference dedicated to connecting smallcap and microcap companies with qualified investors. The Q2 Investor Summit Group will take place in-person, featuring 65+ companies and over 300 investors comprising institutional investors, family offices, and high net worth investors. Sectors Participating: Biotech, Communication Services, Consumer, Energy, Energy/Tech, Financial, Healthcare, Industrials, Materials, Real Estate, Technology, and Tech/Crypt. [email protected]

SOURCE: Panacea Life Sciences, Inc

Panacea Life Sciences Establishes Scientific Advisory Board Dedicated to Cannabinoid Science Research to Support Clinical Strategy and Product Development

GOLDEN, CO / ACCESSWIRE / April 28, 2022 / Panacea Life Sciences, Inc. (OTCQB:PLSH), (“Panacea” or the “Company”), a Colorado, USA-based cannabinoid research and certified GMP manufacturing company is pleased to announce the formation of its Scientific Advisory Board (“SAB”) comprised of six carefully selected key opinion leaders and/or subject matter experts. This strategic group will serve multiple purposes for Panacea, including providing external and objective guidance on cannabinoid products, studies, and proposed directions.

As the company makes their push toward producing more purposeful, biomedical cannabinoid medicine products for both humans and pets, the SAB will help Panacea’s scientific efforts by assisting in study design, product and formula validation, participation in workshops, meetings, and panels, and more. To ensure a well-rounded team, Panacea sought input from experts from local universities as well as in a variety of areas of studies: skincare, veterinary, chemical and biological engineering, agronomy, and medical.

Graphical user interface, text, application, TeamsDescription automatically generated

The members of the Panacea Life Sciences Scientific Advisory Board are:

Paul Dean, M.D. – Dermatologist

Dr. Dean earned his medical degree in 1968 from the University of California in San Francisco. After a 1-year residency in Internal Medicine, Dr. Dean joined the Centers for Disease Control where he trained epidemiology. His role at the CDC enabled him to participate in numerous public health undertakings and epidemic research studies. These experiences prompted him to complete the educational program at UCLA School of Public Health, where he received his master’s degree in public health. After achieving board certification from the American Board of Dermatology in 1976, Dr. Dean began his clinical dermatology practice in La Mesa, where he has served patients ever since. In addition to performing general dermatology services for more than 25 years, Dr. Dean has also been actively involved in the development of skin care products. His SkinResource.MD line, formulated to prevent, control, and reverse the signs of aging, was established in 2007. In 2019, he launched VitaFit, a skincare line dedicated to the needs of amputees and diabetics. Most recently, Dr. Dean has started to work with CBD skin care products that he feels will bring even better results to his patients.

Larry Good, M.D. – Gastroenterologist

Dr. Larry Good has been a practicing gastroenterologist since 1978. Dr. Good graduated Colgate University Magna Cum Laude in 1969 and received his M.D. with Alpha Omega Alpha status from the Medical University of South Carolina in Charleston, SC in 1973. He served a medical residency from 1973-76 and was Chief Medical Resident in 1976. Dr. Good has served as the Director of Liver Diseases at Nassau County Medical Center and was for many years Chief, Division of Gastroenterology, Department of Medicine at South Nassau Communities Hospital. From 2014 to 2016, Dr. Good has given hundreds of lectures in his field and has authored numerous papers and abstracts. His recent clinical research activities involve the microbiome, inflammatory bowel disease, irritable bowel syndrome and the application of orally administered gamma globulin to patients with acute and chronic gastro-intestinal disorders. Dr. Good founded Good Pharmaceutical Development Co., LLC, in 2014. He is their CEO and is developing a topical product for treating neuropathic pain. This includes cannabinoid and currently available generic FDA approved products in novel preparations. In May 2016, Dr. Good was named to the Steering Committee of the Lambert Center for Hemp and Marijuana Research at Thomas Jefferson University in Philadelphia. Dr. Good has authored and co-authored pivotal studies in peer reviewed journals regarding medical application of cannabinoids. He has also been very active in CME programs for cannabinoid education. Dr. Good delivered the keynote address on the endocannabinoid system at the 2019 annual meeting of the NYS Pain Society and has been invited to Chair the Controversies in Pain Management Panel at the 2020 meeting. Most recently, Dr. Good has engineered the development of PainTx and brought this unique, high concentration topical cream successfully to market and continues to expand new products including CBD and CBDa combinations for safe and effective pain relief.

Janice Knox, M.D.- General Practitioner

Dr. Knox spent 32 years as a board-certified anesthesiologist before becoming an Endocannabinolist and Cannabinoid medicine specialist. As a cofounder of the American Cannabinoid Clinics, Dr Janice resonates the importance to understand the pharmacology of cannabis and the intricate physiology of the endocannabinoid system and create better products and services because of that understanding. She firmly believes that clinical applications of cannabis and other botanicals will disrupt the way healthcare is practiced today. Dr. Knox is the CEO of the AC Group Inc., Oregon representative of the DFCR, and board member of the American Academy of Cannabinoid Medicine and Association of Cannabis Specialists.

Stephanie McGrath, D.V.M. – Small Animal Veterinarian

Dr. McGrath is an Associate Professor in the Clinical Sciences Department and head of the Neurology Service at Colorado State University’s College of Veterinary Medicine and Biomedical Sciences. She is board-certified in veterinary neurology and, for the past 15 years, has been working in the highly specialized field of medical and surgical neurology. Dr. McGrath’s research has been dedicated to finding novel treatments for canine epilepsy, canine brain tumors, cognitive dysfunction, and canine inflammatory central nervous system diseases. For the past six years, her research efforts have been primarily focused on cannabis, both in a laboratory setting and with clinical trials utilizing client-owned animals with naturally occurring diseases. Her groundbreaking cannabis research and expertise is highly regarded and internationally recognized. She has been successful in generating and utilizing pre-clinical data to perform clinical trials in a variety of naturally occurring canine and feline diseases, most of which serve as a strong translational model for humans. Most recently, Dr. McGrath was granted the 2020 Zoetis Award for Research Excellence, honoring her impactful, innovative, and successful research program.

Nathan Morris, M.D. – General Practitioner

Nathan Morris is the Chief Medical Officer of Atrium Innovations Pro Brands. He resides in Monument, CO where he has a multidisciplinary functional medicine practice, Good Medicine, which focuses on making the complex simple. Dr. Morris is certified by the Institute for Functional Medicine and has practiced root cause medicine for well over a decade. He is actively involved in the evolution of PureGenomics®, which he envisioned and co-created with Kelly Heim, Ph.D. He is also a partner with MBN Systems, which supports the implementation of systems-based medical training in medical schools and residencies. He also co-hosts the podcast Good Medicine on the Go where he explores personalization, technology, and practice implementation strategies. His most recent season explored the history, mechanism of action, and clinical application of cannabis. Dr. Morris is excited about the future of medicine as he helps create the future of personalization and its evolution as it empowers patients to understand their uniqueness and strengths.

Melissa Reynolds, Ph.D. – Analytical Chemist, Head of CRC

Melissa Reynolds, Ph.D., serves as the Director of the Panacea Life Sciences Cannabinoid Research Center and the Faculty Director for Research Cores in the Office of the Vice President for Research at Colorado State University. She is also a professor in Chemistry and Biomedical Engineering at Colorado State University. She received a B.S. In Chemistry from Washington State University and a PH.D. from the University of Michigan and worked for a translational biomedical device company before joining CSU in 2009. Her research interests are in improving medical device technologies to improve patient outcomes. Her group is highly multidisciplinary and collaborative, working in the areas of metal organic frameworks as biocatalysts, antibacterial materials and biosensors. She has been recognized as an emerging investigator by the Journal of Materials Chemistry, a Webb-Waring Biomedical Research Early Career Award, and has received an NSF CAREER Award and a Monfort Award. The group’s research on metal organic frameworks received a 2013 TechConnect National Innovation Award. Her research has been funded by NSF, NIH, DOD, Boettcher Foundation, state funding, and corporate funding. In addition to her research, Reynolds loves the classroom and was named 2011 Educator of the Year by the Colorado Bioscience Association. She continues to actively engage with industry and serves as the executive editor for the SurFACTS, the Surfaces in Biomaterials newsletter.

Meeting quarterly, Panacea intends to discuss direction, data, new studies or collaborations and more. Commenting on the newly formed Scientific Advisory Board, Panacea’s own Chief Scientific Officer, Dr. James Baumgartner said: “Panacea’s focus on research and science are at the cornerstone of what differentiates us from most others in the industry. Assembling this quality Scientific Advisory Board brings hundreds of years of medical expertise and research experience to this emerging market which allows us to develop natural, purposeful products to consumers that are truly backed by science.”

About Panacea Life Sciences Holdings, Inc.

Panacea Life Sciences Holdings, Inc. is a seed to sale cannabinoid manufacturer and research company that produces purposeful, natural medicine for consumers and pets. Panacea sells softgels, gummies, tinctures, sublingual tablets, cosmetics, and other topicals. If you would like more information about this topic or to learn more about Panacea and its products or our land-to-brand practices, please visit www.panacealife.com.

Cautionary Note Regarding Forward-Looking Statements

This press release contains forward-looking statements within the meaning of the Private Securities Litigation Reform Act of 1995, including statements regarding the effectiveness of CBD and other cannabinoids improving the lives of people and pets. You can identify forward-looking statements by use of the words “may,” “will,” “should,” “plans,” “explores,” “expects,” “anticipates,” “continue,” “estimate,” “project,” “intends,” and similar expressions. Forward-looking statements involve risks and uncertainties that could cause actual results to differ materially from those projected or anticipated. These risks and uncertainties include, but are not limited to, risks arising from supply chain disruptions on our ability to obtain raw materials as well as similar problems with our vendors, the impact of the pandemic including new variants on the national and global economy, the impact on the Russian invasion of Ukraine on the global economy, lack of available funding at sufficient levels to meet our working capital needs, competition from third parties; intellectual property rights of third parties; regulatory constraints, including the need for FDA approval under certain circumstances; and changes in technology and methods of marketing; as well as those risks and uncertainties described by us in our annual report on Form 10-K for the fiscal year ended December 31, 2021 under the heading “Risk Factors”. Any forward-looking statement made by us herein speaks only as of the date on which it is made. Factors or events that could cause our actual results to differ may emerge from time to time, and it is not possible for us to predict all of them. We undertake no obligation to publicly update any forward-looking statement, whether as a result of new information, future developments, or otherwise, except as may be required by law.

Contact:
Nick Cavarra
[email protected]

SOURCE: Panacea Life Sciences, Inc

Panacea Life Signs Exclusive Manufacturing Agreement with Good Pharmaceutical Development Co.

GOLDEN, CO / ACCESSWIRE / April 21, 2022 / Panacea Life Sciences, Inc. (OTCQB:PLSH), (“Panacea” or the “Company”), a Colorado, USA-based cannabinoid research and certified GMP manufacturing company has signed an exclusive product manufacturing agreement with Good Pharmaceutical Development Co. (Good Pharma) to produce their proprietary, highly concentrated line of Remei (formerly known as PainTX) CBD products for chronic pain.

Panacea Life Sciences, Inc, Thursday, April 21, 2022, Press release picture

Good Pharma has developed a proprietary, patented delivery system that has been demonstrated to effectively deliver high concentrations of hemp-derived CBD to areas of pain without detectable levels of CBD in the serum. Thousands of patients have been successfully treated with this unique product which contains 2200mg of CBD per ounce, making it the highest concentration available in a topical CBD cream.

Good Pharma was seeking a “full-service” CBD manufacturing operation that can provide premium CBD raw materials, manufacturing, R&D, and fulfillment services all under one roof. Panacea is but only a handful of CBD companies with the operational capacity and expertise to meet their needs in the industry.

The new Remei line of products will utilize Panacea’s PANA Pure® CBD to upgrade and improve the efficacy and quality of their products, as well as Panacea’s manufacturing and distribution services to increase sales and improve operational efficiencies.

“I’m delighted to commence the new phase of product development and manufacturing of our award winning chronic pain relief cream with Panacea Life Sciences,” said Dr. Larry Good, MD, founder and CEO of Good Pharmaceutical Development Co. “Panacea is years ahead in their industry knowledge and expertise in the CBD formulation space, and we felt very strongly that their management team and science-based operations would propel Remei to new heights.”

About Good Pharmaceutical Development Co, LLC.
Good Pharmaceutical Development Co, LLC, was founded in 2015 with the mission to create topical non-systemic alternatives for the treatment of chronic pain. Our Board Members, Larry I. Good, MD, Mike Ferguson, and S. Andaz, MD have lifetimes of clinical experience, clinical and basic science research, and pharmaceutical development experience.

About Panacea Life Sciences Holdings, Inc.
Panacea Life Sciences Holdings, Inc. is a seed to sale cannabinoid manufacturer and research company that produces purposeful, natural medicine for consumers and pets. Panacea sells softgels, gummies, tinctures, sublingual tablets, cosmetics, and other topicals. If you would like more information about this topic or to learn more about Panacea and its products or our land-to-brand practices, please visit www.panacealife.com.

Cautionary Note Regarding Forward-Looking Statements
This press release contains forward-looking statements within the meaning of the Private Securities Litigation Reform Act of 1995, including statements regarding the effectiveness of CBD and other cannabinoids improving the lives of people and pets. You can identify forward-looking statements by use of the words “may,” “will,” “should,” “plans,” “explores,” “expects,” “anticipates,” “continue,” “estimate,” “project,” “intends,” and similar expressions. Forward-looking statements involve risks and uncertainties that could cause actual results to differ materially from those projected or anticipated. These risks and uncertainties include, but are not limited to, risks arising from supply chain disruptions on our ability to obtain raw materials as well as similar problems with our vendors, the impact of the pandemic including new variants on the national and global economy, the impact on the Russian invasion of Ukraine on the global economy, lack of available funding at sufficient levels to meet our working capital needs, competition from third parties; intellectual property rights of third parties; regulatory constraints, including the need for FDA approval under certain circumstances; and changes in technology and methods of marketing; as well as those risks and uncertainties described by us in our annual report on Form 10-K for the fiscal year ended December 31, 2021 under the heading “Risk Factors”. Any forward-looking statement made by us herein speaks only as of the date on which it is made. Factors or events that could cause our actual results to differ may emerge from time to time, and it is not possible for us to predict all of them. We undertake no obligation to publicly update any forward-looking statement, whether as a result of new information, future developments, or otherwise, except as may be required by law.

CONTACT:
Nick Cavarra
[email protected]

SOURCE: Panacea Life Sciences, Inc

Panacea Life Sciences, Inc. Launches Innovative New CBD Horse Paste

GOLDEN, CO / ACCESSWIRE / April 12, 2022 / Panacea Life Sciences, Inc. (OTCQB:PLSH), (“Panacea” or the “Company”), a Colorado, USA-based cannabinoid research and certified GMP manufacturing company providing natural, non-habit-forming health and wellness products for people and pets, announces the launch of their new Calmolyte CBD Horse Paste.

According to Grand View Research’s CBD Pet Market Size & Growth Report, 2021-2028, “The global CBD pet market size was valued at $125.00 million in 2020 and is expected to expand at a compound annual growth rate of 58.9% from 2021 to 2028.” While a majority of the pet CBD products are made for dogs and cats, Panacea saw the opportunity to help the equine segment as well while capitalizing on the rapid growth of the market.

“We have spent a year in product development working with veterinarians and our partners at Colorado State University to develop an effective, naturally calming product for horse owners,” comments James Baumgartner, Panacea’s Chief Science Officer.

The new PANA Pet® Calmolyte Horse Paste is designed to provide relief for the everyday stresses and/or injuries that come up for horses. Whether it is a young horse in training, a new trailer ride or boarding facility, or a nagging injury, Calmolyte may help to bring stress levels and inflammation down naturally.

Panacea’s Director of Research and Development, Doug Grego, commented, “We wanted to formulate a product that would allow us the flexibility to include different vitamins and minerals while carrying a significant dosage of CBD isolate.”

This innovative CBD paste contains ingredients like B vitamins and beneficial minerals that help encourage water consumption and replenish electrolytes lost by a hardworking horse, as well as L-Tryptophan, Ginger Root, and Valerian Root, all known for their calming effects. There is also 1000mg of CBD and Magnolia extract, which both have anti-inflammatory and antioxidative properties to aid in body aches and pains. The thoughtful and well-rounded balance of ingredients help keep horses healthy and happy.

Panacea provides several pet CBD products ranging from softgels and oil drops to creams and tablets, suitable for dogs, cats, horses and small pets. The other PANA categories include a wide variety of organic, powerful, and purposeful human cannabinoid products which can be viewed and purchased at panacealife.com.

About Panacea Life Sciences Holdings, Inc.

Panacea Life Sciences Holdings, Inc. is a seed to sale cannabinoid manufacturer and research company that produces purposeful, natural medicine for consumers and pets. Panacea sells softgels, gummies, tinctures, sublingual tablets, cosmetics, and other topicals. If you would like more information about this topic or to learn more about Panacea and its products or our land-to-brand practices, please visit www.panacealife.com.

Cautionary Note Regarding Forward-Looking Statements

This press release contains forward-looking statements within the meaning of the Private Securities Litigation Reform Act of 1995, including statements regarding the effectiveness of CBD and other cannabinoids improving the lives of people and pets. You can identify forward-looking statements by use of the words “may,” “will,” “should,” “plans,” “explores,” “expects,” “anticipates,” “continue,” “estimate,” “project,” “intends,” and similar expressions. Forward-looking statements involve risks and uncertainties that could cause actual results to differ materially from those projected or anticipated. These risks and uncertainties include, but are not limited to, risks arising from supply chain disruptions on our ability to obtain raw materials as well as similar problems with our vendors, the impact of the pandemic including new variants on the national and global economy, the impact on the Russian invasion of Ukraine on the global economy, lack of available funding at sufficient levels to meet our working capital needs, competition from third parties; intellectual property rights of third parties; regulatory constraints, including the need for FDA approval under certain circumstances; and changes in technology and methods of marketing; as well as those risks and uncertainties described by us in our annual report on Form 10-K for the fiscal year ended December 31, 2021 under the heading “Risk Factors”. Any forward-looking statement made by us herein speaks only as of the date on which it is made. Factors or events that could cause our actual results to differ may emerge from time to time, and it is not possible for us to predict all of them. We undertake no obligation to publicly update any forward-looking statement, whether as a result of new information, future developments, or otherwise, except as may be required by law.

Contact:

Nick Cavarra
[email protected]

SOURCE: Panacea Life Sciences, Inc.

Panacea Life Sciences, Inc. Partners with European CBD Market Leader, Chanelle McCoy Health for US Launch

GOLDEN, CO / ACCESSWIRE / March 15, 2022 / Panacea Life Sciences, Inc. (OTCQB:PLSH), (the “Company”), a cGMP certified, vertically integrated premium CBD and cannabinoid company, announces a new commercial partnership with Chanelle McCoy Health (“CMH”), a premium CBD pharmaceutical company, based out of the UK and Ireland. Since Chanelle McCoy Health launched its own CBD brand Pureis®, it has taken the UK market by storm. This exciting new partnership with Panacea has the potential to provide the U.S. market with access to a safer, higher quality, and more efficacious portfolio of certified CBD products that are backed by clinical studies. Chanelle McCoy Health’s dominant brand, supported by governmental authorities including the European Food Safety Authorities (“EFSA”), is differentiated as the first pioneering CBD food supplement backed by formal safety and efficacy clinical studies.

Panacea Life Sciences, Inc, Tuesday, March 15, 2022, Press release picture

Both companies are fully aligned and complimentary across multiple facets of their company visions including their core values of providing the end consumer with products that are safe, efficacious, and of consistently high quality, at competitive market prices. The mutual mission of the alliance is to be recognized across the United States as the premium provider of science-based CBD products, specifically a portfolio of Ultra Pure CBD (0% THC, with no psychoactive effects) products to those segments of the consumer market seeking to eliminate their exposure to THC in CBD products.

Chanelle McCoy Health and Panacea have joined forces to bring together their expertise to launch this new Ultra Pure CBD product in the U.S. The CBD oil products are set poles apart from any potential competitors in that the Ultra Pure formula is manufactured by means of a validated proprietary process that consistently produces product with undetectable THC levels. It is the very first CBD food supplement to be formally backed by safety clinical studies and to use FDA registered raw materials. Pureis® was launched by pharmaceutical trailblazers Lady Chanelle McCoy and Caroline Glynn when they noticed numerous misleading and poor-quality products on the market; at that juncture, the components of their vision began to crystallize with a view to bringing a safe, certified product to the consumer. Their expertise allowed them to carry out clinical safety studies and navigate through complex regulatory landscapes, so much so, they are the very first company to appear on the UK authority list of CBD food supplements that can be legally sold in the UK market.

Commenting on the partnership, Chanelle McCoy Health founders Lady Chanelle McCoy and Caroline Glynn B.Sc., MSc., L.L.M were quoted as saying: “Our company ethos has been about elevating CBD above social stigma by providing products that are backed by clinical studies. Where others chose to invest in expensive marketing campaigns, we chose to focus on advancing the science and research behind CBD through conducting many clinical studies. This investment has been rewarded by the regulatory advancements we have made with the regulators in Europe and the UK. We hope to continue the same journey in the U.S. with our latest collaboration with Panacea. We both share similar values and strive to deliver CBD products that consumers can trust.”

As safety and purity are top priorities for each company’s products, Chanelle McCoy Health backs their Pureis®/CBD products with long-term clinical studies. One such study aimed to provide information on the possible health hazards likely to arise from repeated exposure to their Ultra Pure CBD over a prolonged period of time. With various parameters assessed and a controlled sample of subjects, it was determined Pureis® CBD is suitable and well-tolerated for consumer use. Additionally, the tests demonstrated that Pureis® CBD does not have any mutagenic effects.

Chanelle McCoy Health chose to collaborate with Panacea because of Panacea’s dedication to science and knowledge surrounding cannabinoid products. The ultimate goal is to expand each company’s footprint globally.

James Baumgartner, Panacea’s Chief Science Officer, comments, “Panacea is very excited about the partnership with Chanelle McCoy Health. Their approach to education and commitment to science aligns perfectly with Panacea’s mission to advance our understanding on how cannabinoids impact human and pet health. Pureis’s Ultra Pure CBD will allow for the manufacturing of products that truly have no detectable THC amounts, giving those in a controlled substance testing environment access to the multiple health benefits provided by CBD.”

Bank of America Merrill Lynch has estimated the global consumer market for CBD is set to reach a value of around $39 billion by 2032. Chanelle McCoy Health is leaps ahead of those competitors vying for consumers’ attention since the high-growth space is now calling for much more regulated and superior safety practices and requiring more trustworthy and efficacious product lines on both sides of the Atlantic.

Panacea recently established a presence in Brazil’s cannabis market by partnering with MyPharma2Go. Both partnerships are a testament to Panacea Life Sciences’ strategic execution of their vision to expand their network globally, solidifying their presence as one of the fastest-growing cannabinoid companies.

These 0% THC CBD products will be launched in the U.S. through Panacea as soon as Spring of 2022.

About Chanelle McCoy Health & Pureis®

Lady Chanelle McCoy and partner Caroline Glynn worked together for over a decade in Chanelle Pharma, now Ireland’s largest indigenous pharma company, where they developed the medical business, achieving 2,500+ product licenses and penetrating 96 global markets. They founded Chanelle McCoy Health and later launched the brand Pureis® Ultra Pure CBD driven by their strong belief in CBD’s healing properties and desire to bring a high-quality product to the market supported by clinical trials. The Company has authorization from the UK regulatory body to remain on the market as a CBD food supplement. The company has also received a validated application by the European Union (EU) for authorization of CBD as a food ingredient.

About Panacea Life Sciences Holdings, Inc.

Panacea Life Sciences Holdings, Inc. is a woman-owned, vertically integrated cannabinoid manufacturer and research company that produces purposeful formulations for consumers and pets. Panacea sells an array of products including softgels, gummies, tinctures, sublingual tablets, skin care, and pain management topicals. If you would like more information about this topic or to learn more about Panacea and its products or our land-to-brand practices, please visit www.panacealife.com.

Forward-Looking Statements:

This press release contains forward-looking statements within the meaning of the Private Securities Litigation Reform Act of 1995, including statements regarding our agreement with Chanelle McCoy Health and the timing concerning the launch of their products. You can identify forward-looking statements by use of the words “may,” “will,” “should,” “plans,” “explores,” “expects,” “anticipates,” “continue,” “estimate,” “project,” “intends,” and similar expressions. Forward-looking statements involve risks and uncertainties that could cause actual results to differ materially from those projected or anticipated. These risks and uncertainties include, but are not limited to, the appeal of Pureis® to American consumers, risks arising from supply chain disruptions on our ability to obtain raw materials as well as similar problems with our vendors, the impact of the pandemic including new variants on the national and global economy, lack of available funding at sufficient levels to meet our working capital needs, competition from third parties; intellectual property rights of third parties; regulatory constraints, including the need for FDA approval under certain circumstances; and changes in technology and methods of marketing; as well as those risks and uncertainties described by us in our quarterly report on Form 10-Q for the fiscal quarter ended June 30, 2021 under the heading “Risk Factors”. Any forward-looking statement made by us herein speaks only as of the date on which it is made. Factors or events that could cause our actual results to differ may emerge from time to time, and it is not possible for us to predict all of them. We undertake no obligation to publicly update any forward-looking statement, whether as a result of new information, future developments, or otherwise, except as may be required by law.

Contact:

Nick Cavarra
[email protected]

SOURCE: Panacea Life Sciences, Inc.