Imdatifan is under clinical development by NiKang Therapeutics and currently in Phase II for Metastatic Renal Cell Carcinoma. According to GlobalData, Phase II drugs for Metastatic Renal Cell Carcinoma have a 40% phase transition success rate (PTSR) indication benchmark for progressing into Phase III. GlobalData’s report assesses how Imdatifan’s drug-specific PTSR and Likelihood of Approval (LoA) scores compare to the indication benchmarks. Buy the report here.
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.
Imdatifan overview
NKT-2152 under development for the treatment of advanced metastatic clear cell renal cell carcinoma and hepatocellular carcinoma. It acts by targeting hypoxia-inducible factor 2alpha (HIF-2alpha). It is administered through oral route.
NiKang Therapeutics overview
NiKang Therapeutics is developing small molecule drugs for cancer. The company is headquartered in Wilmington, Delaware, the US.
For a complete picture of Imdatifan’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.
