Vepafestinib is under clinical development by Helsinn Healthcare and currently in Phase II for Solid Tumor. According to GlobalData, Phase II drugs for Solid Tumor have a 37% phase transition success rate (PTSR) indication benchmark for progressing into Phase III. GlobalData’s report assesses how Vepafestinib’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.
Vepafestinib overview
Vepafestinib is under development for the treatment solid tumors with RET mutations and non-small cell lung cancer. It is administered through oral route. The drug candidate acts by targeting proto-oncogene tyrosine-protein kinase receptor RET.
The drug candidate was under development for the treatment of papillary and medullary thyroid cancer.
Helsinn Healthcare overview
Helsinn Healthcare, a subsidiary of 3B Future Holding SA, is a pharmaceutical company that provides therapies for cancer and chronic diseases.
For a complete picture of Vepafestinib’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.
