VTX-3232 is under clinical development by Ventyx Biosciences and currently in Phase II for Parkinson’s Disease. According to GlobalData, Phase II drugs for Parkinson’s Disease have a 41% phase transition success rate (PTSR) indication benchmark for progressing into Phase III. GlobalData’s report assesses how VTX-3232’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.
VTX-3232 overview
VTX-3232 is under development for the treatment of neuroinflammation diseases including Parkinson's disease, obesity, multiple sclerosis and atherosclerotic cardiovascular disease. They acts by targeting NACHT, LRR and PYD domains-containing protein 3 (NLRP3). It is administered through oral route.
Ventyx Biosciences overview
Ventyx Biosciences is a clinical stage biopharmaceutical company focused on developing oral medicines for patients suffering with autoimmune and inflammatory disorders. The company is headquartered in San Diego, California, the US.
For a complete picture of VTX-3232’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.
