NX-1607 is under clinical development by Nurix Therapeutics and currently in Phase I for Solid Tumor. According to GlobalData, Phase I drugs for Solid Tumor have a 54% phase transition success rate (PTSR) indication benchmark for progressing into Phase II. GlobalData’s report assesses how NX-1607’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.
NX-1607 is under development for the treatment of solid tumors including melanoma, epithelial ovarian cancer, gastric cancer, head and neck squamous cell carcinoma, non-small cell lung cancer, metastatic castration resistant prostate cancer, diffuse large b-cell lymphoma with Richter transformation, cervical cancer, metastatic colorectal cancer, fallopian tube cancer, peritoneal cancer, metastatic urothelial cancer, malignant pleural mesothelioma and adenocarcinoma of the gastroesophageal junction. It is administered by oral route. It act by targeting casitas B lineage lymphoma proto-oncogene b (CBL-b). The drug candidate is developed based on DEligase platform.
For a complete picture of NX-1607’s drug-specific PTSR and LoA scores, buy the report here.