Anti-GPRC5D CAR T-cell Therapy is under clinical development by Protheragen and currently in Phase I for Relapsed Multiple Myeloma. According to GlobalData, Phase I drugs for Relapsed Multiple Myeloma have a 78% phase transition success rate (PTSR) indication benchmark for progressing into Phase II. GlobalData’s report assesses how Anti-GPRC5D CAR T-cell Therapy’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.
Anti-GPRC5D CAR T-cell Therapy overview
Protheragen discovers and develops therapies to treat cancers. The company is investing CD3XCD20 bsAb, an antibody therapy for the treatment of lymphomas; MUC1-Ab targeting acute myelocytic leukemia; LAG3-Ab and OX40-Ab to treat cancers; P75NEURO, against neurological diseases; P11 for the treatment of type 2 diabetes; and TT-173 against surgical bleeding and trauma. It is also developing therapies to treat nonalcoholic steatohepatitis, hepatitis B, epilepsy, Alzheimer’s disease and Psoriasis. Protheragen’s proprietary cyclic peptide information technology enables discovery of peptide therapeutics. The company provides project collection, transfer, collaboration and fundraising services. It operates in China. Protheragen is headquartered in New York, the US.
For a complete picture of Anti-GPRC5D CAR T-cell Therapy’s drug-specific PTSR and LoA scores, buy the report here.