ZX-4081 is under clinical development by Hangzhou Zenshine Pharmaceuticals and currently in Phase I for Ovarian Cancer. According to GlobalData, Phase I drugs for Ovarian Cancer have a 73% phase transition success rate (PTSR) indication benchmark for progressing into Phase II. GlobalData’s report assesses how ZX-4081’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.
ZX-4081 overview
ZX-4081 is under development for the treatment of solid tumors including breast cancer, urothelial cancer, ovarian cancer, melanoma, non-small cell lung cancer, renal cell carcinoma, head and neck squamous cell cancer, colorectal cancer and hepatocellular carcinoma, inflammation and unspecified indication. The therapeutic candidate act by inhibiting phosphoinositide 3 kinase catalytic gamma polypeptide (PI3Kgamma). It is administered through oral route.
For a complete picture of ZX-4081’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.
