CK-0045 is under clinical development by CytoKi Pharma and currently in Phase I for Obesity. According to GlobalData, Phase I drugs for Obesity have a 59% phase transition success rate (PTSR) indication benchmark for progressing into Phase II. GlobalData’s report assesses how CK-0045’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.
CK-0045 overview
CytoKi Pharma overview
CytoKi Pharma is a clinical-stage biotechnology company that develops protein drugs for epithelial injury such as inflammatory bowel disease (IBD). The company’s lead drug candidate Interleukin-22 (IL-22) treats a broad range of diseases involving the gut-brain-liver axis such as type-2 diabetes, obesity and non-alcoholic fatty liver disease (NAFLD). Its funding partners include ND Capital, Lundbeck Foundation, Seventure Partners and Ysios Capital Partner. Cytoki Pharma is headquartered in Copenhagen, Denmark.
For a complete picture of CK-0045’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.
