TNG-462 is under clinical development by Tango Therapeutics and currently in Phase II for Malignant Mesothelioma. According to GlobalData, Phase II drugs for Malignant Mesothelioma have a 42% phase transition success rate (PTSR) indication benchmark for progressing into Phase III. GlobalData’s report assesses how TNG-462’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.
TNG-462 is under development for the treatment of solid tumors with MTAP (methylthioadenosine phosphorylase) deletion include non-small cell lung cancer, squamous non-small cell lung cancer, mesothelioma. The drug candidate is a next-generation protein arginine methyl transferase 5 (PRMT5) inhibitor. It is administered through oral route.
It was also under development for malignant peripheral nerve sheath tumor (MPNST) and cholangiocarcinoma.
Tango Therapeutics overview
Tango Therapeutics is a biotechnology company that discovers and develops novel drug targets for the treatment of cancer. The company is investigating TNG908, a synthetic lethal small molecule inhibitor of protein arginine methyltransferase 5 (PRMT5) against methylthioadenosine phosphorylase (MTAP) deleted cancers. It also develops PRMT5 TNG462 for MTAP-deleted tumors; CoREST TNG260 for STK11-mutant cancers; USP1 TNG348 for BRCA1 and BRCA2-mutant and HRD+ cancers. It works in collaboration with Gilead Sciences to discover, develop, and commercialize cancer therapies. Tango Therapeutics is headquartered in Boston, Massachusetts, the US.
For a complete picture of TNG-462’s drug-specific PTSR and LoA scores, buy the report here.