ABI-5366 is under clinical development by Assembly Biosciences and currently in Phase I for Genital Herpes. According to GlobalData, Phase I drugs for Genital Herpes have a 59% phase transition success rate (PTSR) indication benchmark for progressing into Phase II. GlobalData’s report assesses how ABI-5366’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.
ABI-5366 overview
ABI-5366 is under development for the treatment of recurrent genital herpes. The drug candidate is a long-acting herpes simplex virus (HSV) helicase-primase inhibitor. It is administered through oral route as a tablet.
Assembly Biosciences overview
Assembly Biosciences (Assembly) is a biotechnology company that develops, discovers and commercializes small molecule therapies. The company develops therapies for the treatment of viral diseases. Its pipeline products include ABI-5366- HSV-2 Long Acting Helicase Inhibitor. It also offers HBV/HDV Entry Inhibitor, Interferon- a Receptor Against, ABI-H3733 and ABI-4334 among others. The company owns and operates in New York, Indiana and California, the US. Assembly is headquartered in South San Francisco, the US.
For a complete picture of ABI-5366’s drug-specific PTSR and LoA scores, buy the report here.
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