Cybin Provides 2021 Year End Summary
Cybin Inc. (NYSE American:CYBN) provided a year-end summary highlighting significant milestones achieved in 2021. The company expanded its workforce from 5 to over 55 employees globally and partnered with nearly 50 organizations, conducting over 90 preclinical studies. Major achievements included FDA approvals for clinical trials, promising data for CYB003 and CYB004, and a successful capital raise of $70M, totaling over $120M since inception. Cybin aims to initiate four first-in-human clinical studies in 2022, focusing on mental health treatments.
- Expanded workforce from 5 to over 55 employees.
- Conducted over 90 preclinical studies and numerous patent filings.
- Raised nearly $70M in capital, totaling over $120M since inception.
- FDA approvals for pivotal clinical trials targeting mental health disorders.
- Promising preclinical data for CYB003 and CYB004.
- None.
"2021 was an exciting year for
2021 Business Highlights:
-
Awarded Notice of Allowance from
U.S. Patent and Trademark Office for CYB004 (deuterated psychedelic tryptamine) for the treatment of anxiety disorders; -
Confirmed Scientific Advice Meeting with
UK Medical and Healthcare Products Regulatory Agency for lead candidate CYB003 for the treatment of major depressive disorder and alcohol use disorder; - Announced FDA Investigational New Drug and Institutional Review Board Approvals for a co-funded investigator-initiated Phase 2 clinical trial evaluating psychedelic-assisted psychotherapy to treat frontline clinicians experiencing COVID-related distress utilizing the EMBARK psychedelic facilitator training program;
-
Awarded Grant for
Psychedelic Treatment Clinic toLenox Hill Hospital to benefit underserved communities.Lenox Hill Hospital , part ofNorthwell Health is the largest healthcare system inNew York State ; -
Announced Positive CYB003 Data demonstrating significant advantages over oral psilocybin for the treatment of mental health disorders. The Company’s deuterated psilocybin analog from its CYB003 program demonstrated a
50% reduction in variability compared to oral psilocybin, a50% reduction in dose compared to oral psilocybin, a50% shorter time to onset when compared to oral psilocybin and nearly double brain penetration when compared to oral psilocybin; -
Granted a Schedule I Manufacturing License from the
U.S. Drug Enforcement Agency for the Company’sBoston -area research lab that is expected to allow the Company to expand its internal research and development capabilities; - Received Approval from FDA for its Investigational New Drug Application to proceed with a Company-sponsored feasibility study using the Kernel Flow quantitative neuroimaging technology to measure ketamine’s psychedelic effect on cerebral cortex hemodynamics;
-
Launched the EMBARK Psychedelic Facilitator Training Program in collaboration with the
University of Washington in preparation for the first clinical trial of psilocybin-assisted psychotherapy to address COVID-19 related distress in frontline healthcare professionals; - Completed 74 In-Vitro and In-Vivo Evaluations of the Company’s expanding portfolio of psychedelic compounds being designed for potential therapeutic applications for several mental health conditions. To date, more than 50 novel compounds have been evaluated;
- Signed Drug Development Agreement with Catalent which employs around 15,000 people, including approximately 2,400 scientists and technicians, at more than 45 facilities;
-
Retained Former FDA Psychiatry Division Director Dr.
Thomas Laughren as aClinical Advisory Board Member; -
Expanded Operations into
Europe and announced the appointment of Dr.Amir Inamdar as Chief Medical Officer for its European Operations; -
Became the
First Psychedelic Company to list on the NYSE American; -
Raised Nearly
through a bought-deal offering and overnight market financing taking the total capital raise since the company’s inception to over$70M ;$120M - Initiated Next Phase of Company’s Digital Therapeutics Platformwhich will better enable the evaluation of patient outcomes through a highly secure, patient-centered data analytics platform for better pre- and post-psychedelic treatments;
-
Commenced Scale-Up of the Company’s European Operations and Research Activities with various academic and clinical research organizations, including the transfer of its intellectual property assets to its recently formed wholly-owned
Ireland subsidiary; - Announced Alcohol Use Disorder and Anxiety Disorders as New Target Indications alongside the Company’s previously announced major depressive disorder target indications;
- Expanded patent portfolio to cover, among other things, novel psychedelic compounds, integration of delivery platforms, methods of use in psychiatric indications, drug discovery pipeline of modified and novel ergolines, tryptamines and phenethylamines;
-
Entered into
Exclusive Research and Development Collaboration agreement withTMS NeuroHealth Centers Inc. , a wholly-owned subsidiary ofGreenbrook TMS Inc. (TSX:GTMS) (NASDAQ:GBNH), which operates 129 outpatient mental health service centers inthe United States .
About
Cautionary Notes and Forward-Looking Statements
Certain statements in this press release constitute forward-looking information. All statements other than statements of historical fact contained in this press release, including, without limitation, statements regarding Cybin’s future, strategy, plans, objectives, goals and targets, and any statements preceded by, followed by or that include the words “believe”, “expect”, “aim”, “intend”, “plan”, “continue”, “will”, “may”, “would”, “anticipate”, “estimate”, “forecast”, “predict”, “project”, “seek”, “should” or similar expressions or the negative thereof, are forward-looking statements. Forward-looking statements in this news release include statements regarding the Company’s proprietary drug discovery platforms, innovative drug delivery systems, novel formulation approaches and treatment regimens to potentially treat psychiatric disorders.
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: implications of the COVID-19 pandemic on the Company’s operations; 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; and the risk factors set out in the Company's management's discussion and analysis for the period ended
Neither the
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Investor & Media:
Vice President, Investor Relations
leah@cybin.com
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