Psilocybin
Cybin Inches Closer to FDA Submission, Increases Losses in Q1
Toronto-based Cybin Inc. (NYSE: CYBN) (NEO: CYBN) increased its losses for its first fiscal quarter of 2023 to C$14.5 million, up from C$13.1 million a…
Toronto-based Cybin Inc. (NYSE: CYBN) (NEO: CYBN) increased its losses for its first fiscal quarter of 2023 to C$14.5 million, up from C$13.1 million a year prior, but company leadership remained bullish that it’s on the right path to gain federal approval in the U.S. for its psychedelic mental health treatments.
Cybin continued investing in research, development, and clinical studies of synthetic psychedelics designed to combat depression and anxiety, including variations of psilocybin and dimethyltryptamine (DMT). Cybin anticipates delivering data on its synthetic version of psilocybin, CYB003, to the U.S. Food and Drug Administration for consideration in the fourth quarter of 2023.
The company also closed an $8.25 million marketed public offering in Q1 to help fund further R&D.
While Cybin’s operating expenses for the quarter hit C$12.7 million, its cash flows were just C$3.5 million, an imbalance that’s unlikely to be resolved until the company can bring at least one new drug to market.
On that front, Cybin this past quarter:
- Launched clinical dosing for CYB003, its synthetic psilocybin, in its sixth batch of patient testing of up to 12 milligrams, which thus far has “shown to have a favorable safety and tolerability profile” with “no serious adverse events.”
- Continued with phase 1 of clinical trials for Cybin’s DMT substitute, CYB004, which is aimed at treating general anxiety disorder. So far, the drug has been found to deliver a psychedelic high within 2 minutes that peaks after 12 minutes, which Cybin is trying to extend to 45-60 minutes. Initial results are expected later this year.
- Announced a new partnership with Worldwide Clinical Trials to further support its psychedelic trials and studies.
- Launched a new psychedelic training program called Embark for health care professionals interested in conducting larger-scale psychedelic studies. So far about 1,500 individuals have registered.
The post Cybin Inches Closer to FDA Submission, Increases Losses in Q1 appeared first on Green Market Report.
psilocybin dmt dimethyltryptamine psychedelic synthetic psychedelics depression anxiety psychedelics investing fund cybin fda research
-
Psychedelics1 week agoCybin Announces Publication of Research Manuscript in the Journal of Medicinal Chemistry
-
Psilocybin1 week agoCalifornia advances bill for psychedelics centers
-
Psilocybin5 days agoPassover Perspectives: Psychedelics, Moses, and the Burning Bush
-
Psychedelics1 week agoRevive Therapeutics Announces FDA Acceptance of Meeting Request for Long COVID Diagnostic Product
-
Psychedelics1 week agoPsychedelics Can Offer More Than Therapy On Its Own
-
Psychedelics4 days agoAlgernon NeuroScience and the Centre for Human Drug Research to Present DMT Phase 1 Stroke Clinical Data at the Interdisciplinary Conference on Psychedelic Research June 6 – 8th, 2024
-
Psychedelics5 days ago
Revive Therapeutics Announces Type C Meeting Request Granted by FDA for Clinical Study of Bucillamine to Treat Long COVID
-
Psychedelics5 days agoSilo Pharma Announces Positive Results for Intranasal PTSD Treatment