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MyMD Announces U.S. Drug Enforcement Administration (DEA) Determines Supera-CBD is not a Controlled Substance or Listed Chemical - DEA scientific review concludes Supera-CBD will not be classified as a regulated chemical

Key Takeaway: MyMD Pharmaceuticals announced that the U.S. Drug Enforcement Administration (DEA) has determined that Supera-CBD is not a controlled substance or listed chemical. This decision allows for unhindered drug development without the regulatory burden of scheduling. Supera-CBD is a synthetic cannabidiol analog believed to be 8000 times more potent as a CB2 agonist than traditional CBD. The company aims to explore its potential therapeutic benefits, including anti-inflammatory effects and applications in managing addiction and chronic pain.

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POSITIVE FACTORS

  • The DEA has ruled Supera-CBD is not a controlled substance, aiding in development.
  • Supera-CBD has shown potential to manage addiction, anxiety, and chronic pain.
  • The product candidate retains safety and tolerability without intoxicating effects.
  • Partnership with Johns Hopkins Medicine for preclinical pain studies enhances credibility.

Full Press Release Details

Announces U.S. Drug Enforcement Administration (DEA) Determines
Supera-CBD is not a Controlled Substance or
DEA scientific review concludes Supera-CBD will not be classified as a
regulated chemical or require scheduling during development
MD - March 2, 2023 - MyMD Pharmaceuticals, Inc. (Nasdaq: MYMD) ("MyMD" or "the
Company"), a clinical stage biopharmaceutical company developing groundbreaking therapies for the treatment of serious and debilitating
autoimmune and inflammatory diseases, today announced that the U.S. Drug Enforcement Administration (DEA) has conducted a scientific
review and determined that investigational cannabinoid Supera-CBD is not currently considered a controlled substance or listed
chemical. The scientific review of the chemical structure of Supera-CBD was conducted in accordance with the Controlled Substances Act
(CSA) and its governing regulations.
all FDA-approved cannabinoid products are considered controlled substances, with the exception of Epidiolex, and although plant-derived
cannabidiol (CBD) is unscheduled, its use by military and federal civilian employees currently is prohibited without a valid prescription.
This decision by the DEA is tremendous news for Supera-CBD and we are very pleased that our product candidate will not require DEA scheduling
during development," said Christopher Chapman, MD, President, Director, and Chief Medical Officer at MyMD Pharmaceuticals. "We
look forward to studying Supera-CBD's potential to improve upon the benefits of CBD while retaining its safety and tolerability
without intoxicating effects."
is a tremendous benefit to be able to conduct drug development without the burden of dealing with a scheduled product." said Dr.
Jack Henningfield, Vice President, Research, Health Policy, and Abuse Liability at Pinney Associates, Inc. "We look forward to
continuing our support of MyMD Pharmaceuticals as Supera-CBD advances through development."
is a synthetic, non-toxic cannabidiol (CBD) analog that is an 8000-times more potent CB2 agonist than plant-based CBD. In addition to
its potential role in managing addiction, anxiety, chronic pain and seizures, Supera-CBD has also been shown in preclinical studies to
have anti-inflammatory effects. Supera-CBD is a unique synthetic analog of CBD whose structure has been modified to be CB2-receptor selective.
Studies to investigate Supera-CBD's binding and affinity to CB1 and CB2 receptors show that the compound had very low affinity
to CB1 and had a four-fold increase in binding to the CB2 receptor in comparison to CBD. Supera-CBD has completed genotoxicity studies
and the company has initiated preclinical pain studies in partnership with Johns Hopkins Medicine.
MyMD Pharmaceuticals
Pharmaceuticals, Inc. (Nasdaq: MYMD), is a clinical stage biopharma company developing groundbreaking therapies for the treatment of
serious and debilitating autoimmune and inflammatory diseases. MyMD's lead clinical candidate, MYMD-1 , is an orally available
next-generation TNF-alpha inhibitor with the potential to transform the way that TNF-alpha based diseases are treated. MYMD-1 , with
its small molecule design, improved safety profile and ability to cross the blood brain barrier, has the promise to provide meaningful
therapeutic solutions to patients not served by current TNF-alpha inhibitors and as a potential therapy for CNS-based inflammatory and
autoimmune diseases. MYMD-1 has demonstrated the potential to slow the aging process and extend healthy lifespan. The company is evaluating
MYMD-1 in Phase 2 studies for sarcopenia/frailty, a result of the aging process, as well as early-stage trials for rheumatoid arthritis
(RA), with the potential to expand into other applications. MyMD's second therapeutic candidate is Supera-CBD, a novel, synthetic,
non-toxic cannabidiol (CBD) analog that is 8000 times more potent a CB2 agonist (activator) than plant-based CBD. In addition to its
potential role in managing addiction, anxiety, chronic pain and seizures, Supera-CBD has also been shown to have anti-inflammatory effects.
For more information, visit www.mymd.com.
Statement Regarding Forward-Looking Statements
press release may contain forward-looking statements. These forward-looking statements involve known and unknown risks, uncertainties
and other factors which may cause actual results, performance or achievements to be materially different from any expected future results,
performance, or achievements. Forward-looking statements speak only as of the date they are made and none of MyMD nor its affiliates
assume any duty to update forward-looking statements. Words such as "anticipate," "believe," "could,"
"estimate," "expect," "may," "plan," "will," "would'' and
other similar expressions are intended to identify these forward-looking statements. Important factors that could cause actual results
to differ materially from those indicated by such forward-looking statements include, without limitation: the timing of, and MyMD's
ability to, obtain and maintain regulatory approvals for clinical trials of MyMD's pharmaceutical candidates; the timing and results
of MyMD's planned clinical trials for its pharmaceutical candidates; the amount of funds MyMD requires for its pharmaceutical candidates;
increased levels of competition; changes in political, economic or regulatory conditions generally and in the markets in which MyMD operates;
MyMD's ability to retain and attract senior management and other key employees; MyMD's ability to quickly and effectively
respond to new technological developments; MyMD's ability to protect its trade secrets or other proprietary rights, operate without
infringing upon the proprietary rights of others and prevent others from infringing on MyMD's proprietary rights; and the impact
of the ongoing COVID-19 pandemic on MyMD's results of operations, business plan and the global economy. A discussion of these and
other factors with respect to MyMD is set forth in the Company's Annual Report on Form 10-K for the year ended December 31, 2021,
filed by MyMD on March 31, 2022, as may be supplemented or amended by the Company's Quarterly Reports on Form 10-Q. Forward-looking
statements speak only as of the date they are made and MyMD disclaims any intention or obligation to revise any forward-looking statements,
whether as a result of new information, future events or otherwise.

Frequently Asked Questions

What did the DEA conclude about Supera-CBD?

The DEA determined that Supera-CBD is not a controlled substance.

Is Supera-CBD classified as a regulated chemical?

No, Supera-CBD will not be classified as a regulated chemical during development.

What are the potential benefits of Supera-CBD?

Supera-CBD may help manage addiction, anxiety, chronic pain, seizures, and has anti-inflammatory effects.

How potent is Supera-CBD compared to plant-based CBD?

Supera-CBD is 8000 times more potent as a CB2 agonist than plant-based CBD.

What is MyMD Pharmaceuticals focusing on?

MyMD Pharmaceuticals develops therapies for autoimmune and inflammatory diseases.

Last updated: Mar 2, 2023