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FSD Pharma Announces Filing of Year-End 2022 Results TORONTO--(BUSINESS WIRE)

Key Takeaway: FSD Pharma Inc. has announced the filing of its Annual Report on Form 20-F for the year ending December 31, 2022, including financial results and management analysis. The company is focused on the development of several drug candidates aimed at treating neurodegenerative and inflammatory disorders. However, the document highlights the inherent risks and uncertainties in drug development, emphasizing that current projects are in early stages and may face significant obstacles.

Market Sentiment Analysis

POSITIVE FACTORS

  • FSD Pharma reported the filing of its Annual Report for year-end 2022.
  • The company is actively developing multiple drug candidates for serious medical conditions.
  • The educational nature of the report allows for increased transparency with investors.

CONCERNS & RISKS

  • FSD Pharma's drug candidates are at very early stages of development, posing significant uncertainty.
  • There is potential for delays in clinical trials and other development activities.
  • There is no guarantee that drug candidates will obtain regulatory approval or succeed in clinical outcomes.

Full Press Release Details

FSD Pharma Announces Filing of Year-End 2022 Results

TORONTO--(BUSINESS WIRE)--March 31, 2023--FSD Pharma Inc. (NASDAQ: HUGE) (CSE: HUGE) (FRA: 0K9A) ("FSD Pharma" or the "Company"), a biopharmaceutical company dedicated to building a portfolio of innovative assets and biotech
solutions for the treatment of challenging neurodegenerative, inflammatory and metabolic disorders, today announced the filing of its Annual Report on Form 20-F for the year ended December 31, 2022, audited financial results for the fourth
quarter and full year then ended and accompanying management discussion and analysis.
These filings are available for review under the Company's SEDAR profile at www.sedar.com and the Company's EDGAR profile at www.sec.gov.
FSD Pharma Inc. is a biotechnology company with three drug candidates in different stages of development. FSD BioSciences, Inc., a wholly owned subsidiary, is focused on pharmaceutical research and development of its lead compound, FSD201, a
proprietary ultra-micronized PEA formulation, for the treatment of inflammatory diseases. Lucid Psychss Inc., a wholly owned subsidiary, is focused on the research and development of its lead compounds, Lucid-Psych and Lucid-MS. Lucid-Psych is
a molecular compound identified for the potential treatment of mental health disorders, and expanding this category, the Company is investigating other products addressing acute medical needs due to the abuse of drugs such as alcohol. Lucid-MS
is a molecular compound identified for the potential treatment of neurodegenerative disorders.
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 FSD Pharma Inc. and are based on certain assumptions that FSD Pharma has
made in respect thereof as of the date of this press release. FSD Pharma cannot give any assurance that such forward-looking statements will prove to have been correct.
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 U.S. Securities and Exchange Commission on EDGAR (www.sec.gov), including the Company's Annual Report on Form 20-F for the fiscal year ended December 31, 2021, under the heading "Risk Factors." This list of risk factors should not be
construed as exhaustive. Readers are cautioned that events or circumstances could cause results to differ materially from those predicted, forecasted or projected. The forward-looking statements contained in this document speak only as of the
date of this document. FSD Pharma does not undertake any obligation to publicly update or revise any forward-looking statements or information contained herein, except as required by applicable laws. The forward-looking statements contained in
this document are expressly qualified by this cautionary statement.
Neither the Canadian Securities Exchange nor its regulation services provider accept responsibility for the adequacy or accuracy of this release.

Contacts

Zeeshan Saeed, Founder, President and Executive Co-Chairman of the Board, FSD Pharma Inc.
Telephone: (416) 854-8884

Frequently Asked Questions

What did FSD Pharma announce on March 31, 2023?

FSD Pharma announced the filing of its Year-End 2022 results and Annual Report.

What are FSD Pharma's main focus areas?

FSD Pharma focuses on neurodegenerative, inflammatory, and metabolic disorders.

What drug candidates does FSD Pharma have?

FSD Pharma has three drug candidates at various development stages.

Where can FSD Pharma's financial reports be accessed?

Financial reports are available on SEDAR and EDGAR profiles.

What potential issues affect FSD Pharma's forecasts?

Risks include uncertainties in drug development and regulatory approvals.

Last updated: Mar 31, 2023