PRT-543 is under clinical development by Prelude Therapeutics and currently in Phase I for Refractory Acute Myeloid Leukemia. According to GlobalData, Phase I drugs for Refractory Acute Myeloid Leukemia have a 68% phase transition success rate (PTSR) indication benchmark for progressing into Phase II. GlobalData’s report assesses how PRT-543’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.
PRT-543 is under development for the treatment of relapsed/refractory solid tumors like HRD+ high grade serous ovarian cancer, breast cancer, head and neck cancer bladder cancer, small cell lung cancer and hematological malignancies like diffuse large B-cell lymphoma, mantle cell lymphoma, myelodysplastic syndrome, refractory acute myeloid leukemia, chronic myelomonocytic leukemia and myelofibrosis. The drug candidate is administered through oral route. It acts by targeting the protein arginine N methyltransferase 5 (PRMT5).
Prelude Therapeutics overview
Prelude Therapeutics (Prelude) is a clinical-stage precision oncology company developing innovative drug candidates targeting critical cancer cell pathways. The company product pipeline includes PRT1419, a potent, selective inhibitor of MCL1, PRT2527, a potent and highly selective CDK9 inhibitor and PRT3645, a next-generation CDK4/6 inhibitor. Prelude others pipeline includes PRT3789 a first-in-class SMARCA2/BRM protein degraded. It also carries out clinical trials. The company serves throughout the US . Prelude is headquartered in Wilmington, Delaware, the United States.
For a complete picture of PRT-543’s drug-specific PTSR and LoA scores, buy the report here.