PV-001 is under clinical development by Posvax and currently in Phase I for Human Papillomavirus Infections. According to GlobalData, Phase I drugs for Human Papillomavirus Infections have an 87% phase transition success rate (PTSR) indication benchmark for progressing into Phase II. GlobalData’s report assesses how PV-001’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.
PV-001 overview
PV-001 is under development for the prevention of human papillomavirus infections with human papillomavirus (HPV) types 6, 11, 16, 18, 31, 33, 45, 52 and 58. It is administered by parenteral route. It is a virus-like particle (VLP) based vaccine.
It was also under development for the treatment of human papillomavirus associated cancer.
For a complete picture of PV-001’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.
