Taletrectinib adipate is under clinical development by AnHeart 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 Taletrectinib adipate’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.
Taletrectinib adipate overview
Taletrectinib (DS-6051b/AB-106) is under development for the treatment of relapsed or refractory solid tumors including k-RAS wild-type colorectal cancer, neuroendocrine tumors, non-small-cell lung carcinoma (NSCLC), primary CNS tumors, brain metastases and pulmonary large-cell neuroendocrine carcinoma (LCNEC). It is administered orally as a capsule. The drug candidate targets tyrosine kinases ROS1 and NTRKs type 1, 2, 3.
AnHeart Therapeutics overview
AnHeart Therapeutics, a subsidiary of AnHeart Therapeutics Hangzhou Co Ltd, is a clinical stage biopharmaceutical company that focuses on oncology drugs to address unmet medical needs and underserved markets. AnHeart Therapeutics is headquartered in New York City, New York, the US.
For a complete picture of Taletrectinib adipate’s drug-specific PTSR and LoA scores, buy the report here.