Canocapavir is under clinical development by Shanghai Zhimeng Biopharma and currently in Phase I for Hepatitis B. According to GlobalData, Phase I drugs for Hepatitis B have a 71% phase transition success rate (PTSR) indication benchmark for progressing into Phase II. GlobalData’s report assesses how Canocapavir’s drug-specific PTSR and Likelihood of Approval (LoA) scores compare to the indication benchmarks. 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.
Canocapavir overview
Canocapavir (ZMH-1505R) is under development for the treatment of chronic Hepatitis B. It is administered by oral route. The drug candidate is a pyrazole-oxazolidinone compound and a novel chemical entity. It acts by inhibiting capsid protein.
Shanghai Zhimeng Biopharma overview
Shanghai Zhimeng Biopharma, Inc., is a biotech company with focus on discovering and developing innovative therapies for treating chronic hepatitis B virus infection and neurological diseases. The company is headquartered in China.
For a complete picture of Canocapavir’s drug-specific PTSR and LoA scores, buy the report here.
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