XYF-19 is under clinical development by Xi’An Yufan Biotechnology and currently in Phase I for Chronic Lymphocytic Leukemia (CLL). According to GlobalData, Phase I drugs for Chronic Lymphocytic Leukemia (CLL) have a 69% phase transition success rate (PTSR) indication benchmark for progressing into Phase II. GlobalData’s report assesses how XYF-19’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.
XYF-19 overview
XYF-19 is under development for the treatment of relapsed/refractory B cell hematological malignancies including B cell acute lymphoblastic leukemia (B-ALL), chronic lymphocytic leukemia (CLL), follicular lymphoma, marginal zone B-cell lymphoma, Waldenstrom macroglobulinemia, hairy cell leukemia, diffuse large B-Cell lymphoma, Burkitt lymphoma and mantle cell lymphoma. It is administered through intravenous route. The therapeutic candidate comprises of autologous T-cells genetically transduced with a lentiviral vector to express chimeric antigen receptors (CAR) targeting cells expressing CD19. The CAR-T cells are electroporated with CRISPR guide RNA to disrupt expression of endogenous HPK1.
For a complete picture of XYF-19’s drug-specific PTSR and LoA scores, buy the report here.
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