FSD Pharma Presenting Two Scientific Posters on Preclinical Toxicology and Efficacy Data of Lucid-21-302 (Lucid-MS) at Americas Committee for Treatment and Research in Multiple Sclerosis (ACTRIMS) 2023 Forum
FSD Pharma (NASDAQ: HUGE) has released a new corporate video aimed at providing insights into its innovative efforts to assist those suffering from Multiple Sclerosis (MS). The company will present at the ACTRIMS 2023 Forum from February 23-25 in San Diego, showcasing its candidate drug Lucid-21-302, which has received Health Canada's approval for a Phase 1 clinical trial. A recent Morningstar report indicates that HUGE has outperformed its peers and is rated 4 stars, with a fair value of CDN$4.58. The report also shows strong bullish sentiment across various timeframes. FSD has also engaged Independent Trading Group for market-making services.
- New corporate video enhances public awareness of FSD Pharma's innovations for MS.
- Attendance at ACTRIMS 2023 Forum to discuss promising drug candidate Lucid-21-302.
- Receipt of No Objection Letter from Health Canada for Phase 1 clinical trial approval.
- Morningstar report highlights HUGE's outperformance and undervalued status.
- Bullish sentiment reported across short, intermediate, and long-term forecasts.
- None.
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FSD Pharma releases new corporate video providing insight on the Company’s innovation to help millions of people suffering from Multiple Sclerosis - Morningstar releases research coverage on HUGE, noting outperformance of peers in recent months and undervalued quantitative valuation
Represented by Dr.
Lucid-MS, a neuroprotective compound with a unique mechanism of action for the treatment of MS, is a patented New Chemical Entity that has shown in preclinical models to prevent myelin degradation (demyelination), a known cause of MS and other neurogenerative diseases characterized by damage to the myelin sheath surrounding nerve fibers in the central nervous system.
The second presentation, “Treatment with Lucid-21-302 Stabilizes Myelin During Cuprizone-Induced Myelin Intoxication and Reduces Myelin and Axon Injury in Experimental Autoimmune Encephalomyelitis,” covers efficacy of Lucid-MS in preclinical research, which demonstrated myelin-protective and neuroprotective effects in immune and non-immune-based models of MS.
Both presentations will occur during the Poster Two Session of ACTRIMS from
Both presentations will be available on the
“ACTRIMS provides us with an opportunity to interact with an esteemed community of leaders pushing the boundaries of Multiple Sclerosis research,” said
Separately, Morningstar has released a research report with coverage of
- HUGE has outperformed its Biotechnology & Drugs peers over the last three months and over the past year.
- HUGE is rated 4 stars out of 5 stars.
- HUGE’s Quantitative Valuation shows Undervalued
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HUGE’s Fair Value of
CDN or$4.58 USD as of$3.48 Feb. 14, 2023 . - Short-Term Sentiment shows Strong Bullish Evidence
- Intermediate-Term Sentiment shows Very Strong Bullish Evidence
- Long-Term Sentiment shows Bullish Evidence
The complete report is available exclusively to Morningstar subscribers.
The Company has retained
FSD has agreed to issue common share purchase warrants to purchase 500,000 shares of the Company. The warrants will expire 13 months after the vesting criteria has been met with an exercise price ranging from
About
Forward Looking Information
This press release contains forward-looking statements and forward-looking information (collectively, "forward-looking statements") within the meaning of applicable securities laws. Any statements that are contained in this press release that are not statements of historical fact may be deemed to be forward-looking statements. Forward-looking statements are often identified by terms such as “plans”, “expects”, “expected”, “scheduled”, “estimates”, “intends”, “anticipates”, “hopes”, “planned” or “believes”, or variations of such words and phrases, or states that certain actions, events or results “may”, “could”, “would”, “might”, “potentially” or “will” be taken, occur or be achieved. More particularly, and without limitation, this press release contains forward-looking statements contained in this press release include statements concerning the future of
Since forward-looking statements relate to future events and conditions, by their very nature they require making assumptions and involve inherent risks and uncertainties. The Company cautions that although it believes the expectations and material factors and assumptions reflected in these forward-looking statements are reasonable as of the date hereof, there can be no assurance that these expectations, factors and assumptions will prove to be correct and these risks and uncertainties give rise to the possibility that actual results may differ materially from the expectations set out in the forward-looking statements. These forward-looking statements are not guarantees of future performance and are subject to a number of known and unknown risks and uncertainties including, but not limited to: the fact that the drug development efforts of both Lucid and FSD BioSciences are at a very early stage; the fact that preclinical drug development is uncertain, and the drug product candidates of Lucid and FSD BioSciences may never advance to clinical trials; the fact that results of preclinical studies and early-stage clinical trials may not be predictive of the results of later stage clinical trials; the uncertain outcome, cost, and timing of product development activities, preclinical studies and clinical trials of Lucid and FSD BioSciences; the uncertain clinical development process, including the risk that clinical trials may not have an effective design or generate positive results; the potential inability to obtain or maintain regulatory approval of the drug product candidates of Lucid and FSD BioSciences; the introduction of competing drugs that are safer, more effective or less expensive than, or otherwise superior to, the drug product candidates of Lucid and FSD BioSciences; the initiation, conduct, and completion of preclinical studies and clinical trials may be delayed, adversely affected, or impacted by COVID-19 related issues; the potential inability to obtain adequate financing; the potential inability to obtain or maintain intellectual property protection for the drug product candidates of Lucid and FSD BioSciences; and other risks. Accordingly, readers should not place undue reliance on the forward-looking statements contained in this press release, which speak only as of the date of this press release.
Further information regarding factors that may cause actual results to differ materially are included in the Company’s annual and other reports filed from time to time with the Canadian Securities Administrators on SEDAR (www.sedar.com) and with the
Neither the Canadian Securities Exchange nor its regulation services provider accept responsibility for the adequacy or accuracy of this release.
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Email: Zsaeed@fsdpharma.com
Telephone: (416) 854-8884
Investor Relations:
Email: ir@fsdpharma.com, info@fsdpharma.com
Website: www.fsdpharma.com
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