OCE-205 is under clinical development by Ocelot Bio and currently in Phase I for Ascites. According to GlobalData, Phase I drugs for Ascites have an 86% phase transition success rate (PTSR) indication benchmark for progressing into Phase II. GlobalData’s report assesses how OCE-205’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.
OCE-205 overview
OCE-205 is under development for the treatment of hepatorenal syndrome with acute kidney injury (HRS-AKI) and ascites. The drug candidate is a peptide therapeutic. It is administered through intravenous route as solution. It acts by targeting vasopressin V1a receptor.
Ocelot Bio overview
Ocelot Bio is a clinical-stage biopharmaceutical company focused on the development of therapeutics for patients with liver disease. Ocelot Bio is headquartered in San Diego, California, the US.
For a complete picture of OCE-205’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.
