XBH-25 is under clinical development by GV20 Therapeutics and currently in Phase I for Endometrial Cancer. According to GlobalData, Phase I drugs for Endometrial Cancer have an 81% phase transition success rate (PTSR) indication benchmark for progressing into Phase II. GlobalData’s report assesses how XBH-25’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.
XBH-25 overview
XHB-25 is under development for the treatment of advanced or refractory solid tumor malignancies, bladder urothelial carcinoma, bile duct cancer (cholangiocarcinoma), adenocarcinoma of the colon or rectum, endometrial carcinoma, head and neck squamous cell carcinoma, cutaneous melanoma, non-small cell lung cancer. It is administered through intravenous route and is being developed based on GV20 genomics and GV20 artificial intelligence (AI) platform. It acts by targeting IGSF8 (Immunoglobulin Superfamily Member 8).
GV20 Therapeutics overview
GV20 Therapeutics develops novel cancer immunology drugs and antibody therapeutics utilizing functional genomics and artificial intelligence platform to exploit vulnerabilities in cancer biology. GV20 Therapeutics is headquartered in Cambridge, Massachusetts, the US.
For a complete picture of XBH-25’s drug-specific PTSR and LoA scores, buy the report here.
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