JWK-004 is under clinical development by Chengdu Genevector Biotechnology 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 JWK-004’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.
JWK-004 overview
JWK-004 is under development for the treatment of hemophilia B. The therapeutic candidate comprises adeno-associated viral (AAV) vector delivering the gene responsible for the treatment of hemophilia B. It acts by targeting coagulation factor IX. It is administered through intravenous route.
Chengdu Genevector Biotechnology overview
Chengdu Genevector Biotechnology (Genevector) is a healthcare service provider which provides gene therapy solutions for multiple diseases. Genevector is headquartered in Chengdu, Sichuan, China.
For a complete picture of JWK-004’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.
