CLV-100 is under clinical development by Cytopeutics and currently in Phase II for Graft Versus Host Disease (GVHD). According to GlobalData, Phase II drugs for Graft Versus Host Disease (GVHD) have a 48% phase transition success rate (PTSR) indication benchmark for progressing into Phase III. GlobalData’s report assesses how CLV-100’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.
CLV-100 overview
CLV-100 is under development for the treatment of acute graft versus host disease. It is administered through intravenous, intramuscular, intraarticular and intracoronary route. It was under development for cerebral artery infarction, wounds, chronic critical limb ischemia, osteoarthritis of knee and ischemic dilated cardiomyopathy.
It was also under development for the treatment of COVID-19 infection complicated by acute respiratory distress syndrome and periodontitis.
For a complete picture of CLV-100’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.
