FKPC-101 is under clinical development by CellVax Therapeutics and currently in Phase II for Metastatic Prostate Cancer. According to GlobalData, Phase II drugs for Metastatic Prostate Cancer have a 32% phase transition success rate (PTSR) indication benchmark for progressing into Phase III. GlobalData’s report assesses how FKPC-101’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.
FKPC-101 overview
FK-PC101 is under development for the treatment of metastatic prostate cancer. The therapeutic candidate comprises irradiated autologous tumor cells which are administered through intradermal route. The drug candidate is being developed based on a proprietary autologous tumor cell-based cancer immuno-therapy platform.
CellVax Therapeutics overview
CellVax Therapeutics developing proprietary cell-based cancer immunotherapy candidate FK-PC101, for the treatment of prostate cancer patients.
For a complete picture of FKPC-101’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.
