SR-604 is under clinical development by Equilibra Bioscience and currently in Phase I for Hemophilia B (Factor IX Deficiency). According to GlobalData, Phase I drugs for Hemophilia B (Factor IX Deficiency) have a 97% phase transition success rate (PTSR) indication benchmark for progressing into Phase II. GlobalData’s report assesses how SR-604’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.

SR-604 overview

SR-604 is under development for the treatment of hemophilia A and hemophilia B. It is administered through subcutaneous route.

Equilibra Bioscience overview

Equilibra Bioscience, a biotechnology company which focuses on developing and commercializing novel therapeutics for the treatment of diseases that are caused by dysregulated metabolism. The company is headquartered in Naples, Florida, the US.

For a complete picture of SR-604’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.