OD-07656 is under clinical development by Odyssey Therapeutics and currently in Phase I for Spondyloarthritis (Spondyloarthropathy). According to GlobalData, Phase I drugs for Spondyloarthritis (Spondyloarthropathy) 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 OD-07656 LoA Report. Buy the report here.
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
OD-07656 is under development for the treatment of crohn disease, ulcerative colitis, blau syndrome, inflammatory bowel diseases, spondyloarthritis. The drug candidate is formulated as capsule administered through oral route and is acts by targeting RIPK2.
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’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.
