PMBCT-01 is under clinical development by PeproMene Bio and currently in Phase I for Marginal Zone B-cell Lymphoma. According to GlobalData, Phase I drugs for Marginal Zone B-cell Lymphoma have an 82% phase transition success rate (PTSR) indication benchmark for progressing into Phase II. GlobalData’s report assesses how PMBCT-01’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.
PMBCT-01 overview
PMBCT-01 is under development for the treatment of B-cell non-Hodgkin lymphoma including Burkitt lymphoma, mantle cell lymphoma and relapsed or refractory B-cell acute lymphoblastic lymphoma (r/r B-ALL) including primary mediastinal large B-cell lymphoma (PMBCL), transformed follicular lymphoma (tFL), and transformed marginal zone lymphoma (tMZL). The therapeutic candidate consists of lentiviral vector comprises of T-cells expressing chimeric antigen receptor (CAR) engineered to express an anti-BAFFR antibody derived single chain fragment (scFv). It acts by targeting TNFRSF13C expressing cells. It is administered through parenteral route.
PeproMene Bio overview
PeproMene Bio., is a developer of novel immune-oncology therapies. The company is headquartered in United States.
For a complete picture of PMBCT-01’s drug-specific PTSR and LoA scores, buy the report here.
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