OD-07656 is under clinical development by Odyssey Therapeutics and currently in Phase I for Crohn’s Disease (Regional Enteritis). According to GlobalData, Phase I drugs for Crohn’s Disease (Regional Enteritis) have an 81% phase transition success rate (PTSR) indication benchmark for progressing into Phase II. GlobalData’s report assesses how OD-07656’s drug-specific PTSR and Likelihood of Approval (LoA) scores compare to the indication benchmarks. 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.
OD-07656 overview
Drug candidates are under development for the treatment of inflammatory and autoimmune diseases like Crohn's disease, ulcerative colitis, Blau syndrome and spondyloarthritis. It acts by targeting interleukin 1 receptor associated kinase 4 (IRAK4). It is administered through oral route.
Odyssey Therapeutics overview
Odyssey Therapeutics is a Pharmaceuticals and Healthcare company that provides immunomodulators and oncology drugs. The Company is Headquartered in San Francisco, California, The U.S.
For a complete picture of OD-07656’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.
