CYB-004 is under clinical development by Cybin and currently in Phase I for Social Anxiety Disorder (SAD/Social Phobia). According to GlobalData, Phase I drugs for Social Anxiety Disorder (SAD/Social Phobia) does not have sufficient historical data to build an indication benchmark PTSR for Phase I. GlobalData uses proprietary data and analytics to create drugs-specific PTSR and LoA in the CYB-004 LoA Report. Buy the report here.
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GlobalData tracks drug-specific phase transition and likelihood of approval scores, in addition to indication benchmarks based off 18 years of historical drug development data. Attributes of the drug, company and its clinical trials play a fundamental role in drug-specific PTSR and likelihood of approval.
CYB-004 overview
CYB-004 is under development for the treatment of social anxiety disorder and generalized anxiety disorder. It is administered through inhalation route, intravenous bolus and intravenous route. The drug candidate is a deuterated forms of DMT and 5-MeO-DMT. It is a deuterated tryptamine and acts by targeting 5-hydroxytryptamine receptor 2A.
Cybin overview
Cybin is a clinical-stage biopharmaceutical company that develops psychedelic drugs to treat mental health conditions. The company’s pipeline products include CYB003, CYB004 and CYB005. Its CYB003 is a deuterated psiloCybin analog that treats major depressive disorder and alcohol use disorder; CYB004 is a deuterated dimethyltryptamine that treats generalized anxiety disorder. Cybin’s CYB005 is a phenethylamine derivative that treats neuroinflammation. The company works in partnership with Clinilabs Drug Development Corporation, the University of Washington and Greenbrook TMS. The company operates in Canada and the US. Cybin is headquartered in Toronto, Ontario, Canada.
For a complete picture of CYB-004’s drug-specific PTSR and LoA scores, buy the report here.
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GlobalData, the leading provider of industry intelligence, provided the underlying data, research, and analysis used to produce this article.
GlobalData’s Likelihood of Approval analytics tool dynamically assesses and predicts how likely a drug will move to the next stage in clinical development (PTSR), as well as how likely the drug will be approved (LoA). This is based on a combination of machine learning and a proprietary algorithm to process data points from various databases found on GlobalData’s Pharmaceutical Intelligence Center.
