Announces Oversubscribed Private Placement of U.S. $150 Million
- Proposed private placement of 348,837,210 common shares at U.S.$0.43 per share.
- Expected gross proceeds of U.S.$150,000,000 before fees and expenses.
- Offering represents a 17% premium to the 10-day volume weighted average trading price on NYSE American.
- Led by Deep Track Capital with participation from RA Capital Management, Avidity Partners, and other institutional investors.
- Proceeds to be used for Phase 3 drug development activities for CYB003 and general corporate purposes.
- CYB003 is a deuterated psilocybin analog for potential treatment of Major Depressive Disorder.
- If approved by FDA, CYB003 would be the first adjunctive psychedelic-based therapeutic for MDD.
- None.
Insights
The announcement of Cybin Inc.'s private placement of common shares at a premium is a significant financial event that underscores investor confidence in the company's potential. The premium price of U.S.$0.43 per common share suggests a strong demand for the stock, indicating positive market sentiment towards Cybin's prospects. The expected aggregate gross proceeds of U.S.$150 million will bolster the company's balance sheet, providing ample funds for the advancement of its Phase 3 drug development activities for CYB003, as well as for working capital and other corporate purposes.
Such capital inflow is critical for a clinical-stage biopharmaceutical company, as the costs associated with bringing a new drug to market are substantial. The involvement of reputable institutional investors like Deep Track Capital and RA Capital Management indicates a level of due diligence that may reassure smaller investors. However, it's important for stakeholders to consider the potential dilution of existing shares due to the increase in the number of common shares. This dilution could affect the stock's value in the short term, although the long-term benefits of successful drug development could offset this impact.
The development of CYB003 as a proprietary deuterated psilocybin analog for the treatment of Major Depressive Disorder (MDD) represents a novel approach in the mental healthcare field. The potential FDA approval of CYB003 as the first adjunctive psychedelic-based therapeutic for MDD could be a game-changer. This is because current treatments for MDD often have limitations, including delayed onset of therapeutic effects and side effects that can reduce patient adherence.
If CYB003 demonstrates efficacy and safety in Phase 3 trials, Cybin Inc. could capture a significant share of the mental health treatment market. The drug's unique mechanism of action, which involves modifying psilocybin's molecular structure to potentially offer better pharmacokinetics, could mean a more favorable safety profile and improved patient outcomes compared to existing treatments. However, the success of this venture hinges on clinical trial results and regulatory approval, which are inherently uncertain in the biopharmaceutical industry.
The mental health treatment market is rapidly evolving, with a growing acceptance of psychedelic-based therapies. Cybin Inc.'s strategic positioning in this sector, particularly with CYB003's advancement to Phase 3 clinical trials, could place the company at the forefront of this emerging industry. The financial backing from institutional investors through the private placement reflects a broader trend of increasing investment in biotech firms focusing on innovative treatments for mental health disorders.
Market analysis indicates a rising demand for new therapeutic options, especially for conditions like MDD, which affect millions globally. The successful development and commercialization of CYB003 could therefore meet a significant unmet medical need, potentially leading to substantial revenue growth for Cybin. It's essential for stakeholders to monitor the competitive landscape and regulatory developments, as these factors will heavily influence the company's market potential and the stock's performance in the long run.
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The oversubscribed Private Placement is being led by Deep Track Capital and includes participation from RA Capital Management, Avidity Partners, Acorn Bioventures, Altium Capital, Logos Capital, Octagon Capital, Rosalind Advisors, Sphera Healthcare and other institutional investors.
The net proceeds of the Private Placement are expected to be used for certain Phase 3 drug development activities for CYB003, working capital and general corporate purposes. CYB003, is a proprietary deuterated psilocybin analog in development for the potential treatment of Major Depressive Disorder (“MDD”). If approved by the
Bloom Burton Securities Inc. is acting as the Lead Agent for the Private Placement, which also includes Haywood Securities Inc. The Private Placement is expected to close on or about March 19, 2024, subject to all necessary regulatory and stock exchange approvals, including the approval of the Cboe Canada and the NYSE American LLC.
In
No securities regulatory authority has either approved or disapproved of the contents of this news release. This news release shall not constitute an offer to sell or the solicitation of an offer to buy nor shall there be any sale of the securities in
About Cybin
Cybin is a clinical-stage biopharmaceutical company on a mission to create safe and effective psychedelic-based therapeutics to address the large unmet need for new and innovative treatment options for people who suffer from mental health conditions.
Cybin’s goal of revolutionizing mental healthcare is supported by a network of world-class partners and internationally recognized scientists aimed at progressing proprietary drug discovery platforms, innovative drug delivery systems, and novel formulation approaches and treatment regimens. The Company is currently developing CYB003, a proprietary deuterated psilocybin analog for the treatment of major depressive disorder and CYB004, a proprietary deuterated DMT molecule for generalized anxiety disorder and has a research pipeline of investigational psychedelic-based compounds.
Headquartered in
Cautionary Notes and Forward-Looking Statements
Certain statements in this news release relating to the Company are forward-looking statements and are prospective in nature. Forward-looking statements are not based on historical facts, but rather on current expectations and projections about future events and are therefore subject to risks and uncertainties which could cause actual results to differ materially from the future results expressed or implied by the forward-looking statements. These statements generally can be identified by the use of forward-looking words such as “may”, “should”, “could”, “intend”, “estimate”, “plan”, “anticipate”, “expect”, “believe” or “continue”, or the negative thereof or similar variations. Forward-looking statements in this news release include statements regarding the sale of any Common Shares pursuant to the Private Placement, the closing of the Private Placement, the use of the net proceeds from the Private Placement, and the Company’s plans to engineer proprietary drug discovery platforms, innovative drug delivery systems, novel formulation approaches and treatment regimens for mental health conditions.
These forward-looking statements are based on reasonable assumptions and estimates of management of the Company at the time such statements were made. Actual future results may differ materially as forward-looking statements involve known and unknown risks, uncertainties, and other factors which may cause the actual results, performance, or achievements of the Company to materially differ from any future results, performance, or achievements expressed or implied by such forward-looking statements. Such factors, among other things, include: fluctuations in general macroeconomic conditions; fluctuations in securities markets; expectations regarding the size of the psychedelics market; the ability of the Company to successfully achieve its business objectives; plans for growth; political, social and environmental uncertainties; employee relations; the presence of laws and regulations that may impose restrictions in the markets where the Company operates; implications of disease outbreaks on the Company's operations; and the risk factors set out in each of the Company's management's discussion and analysis for the three and nine month periods ended December 31, 2023, and the Company’s annual information form for the year ended March 31, 2023, which are available under the Company's profile on www.sedarplus.com and with the
Cybin makes no medical, treatment or health benefit claims about Cybin’s proposed products. The FDA, Health Canada or other similar regulatory authorities have not evaluated claims regarding psilocybin, psychedelic tryptamine, tryptamine derivatives or other psychedelic compounds. The efficacy of such products has not been confirmed by approved research. There is no assurance that the use of psilocybin, psychedelic tryptamine, tryptamine derivatives or other psychedelic compounds can diagnose, treat, cure or prevent any disease or condition. Rigorous scientific research and clinical trials are needed. Cybin has not conducted clinical trials for the use of its proposed products. Any references to quality, consistency, efficacy and safety of potential products do not imply that Cybin verified such in clinical trials or that Cybin will complete such trials. If Cybin cannot obtain the approvals or research necessary to commercialize its business, it may have a material adverse effect on Cybin’s performance and operations.
Neither the Cboe Canada nor the NYSE American LLC stock exchange have approved or disapproved the contents of this news release and are not responsible for the adequacy and accuracy of the contents herein.
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Investors & Media:
Gabriel Fahel
Chief Legal Officer
Cybin Inc.
1-866-292-4601
irteam@cybin.com – or – media@cybin.com
Source: Cybin Inc.
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