Gene Therapy to Target CD19 for Acute Lymphocytic Leukemia and Follicular lymphoma is under clinical development by Shenzhen BinDeBio and currently in Phase II for Follicular Lymphoma. According to GlobalData, Phase II drugs for Follicular Lymphoma have a 43% phase transition success rate (PTSR) indication benchmark for progressing into Phase III. GlobalData’s report assesses how Gene Therapy to Target CD19 for Acute Lymphocytic Leukemia and Follicular lymphoma’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.
Gene Therapy to Target CD19 for Acute Lymphocytic Leukemia and Follicular lymphoma overview
Gene therapy is under development for the treatment of relapsed or refractory B-cell acute lymphocytic leukemia and follicular lymphoma. It is administered through intravenous route.The therapeutic candidate constitutes chimeric antigen receptor (CAR) T cells which act by targeting CD19 TCR-zeta/4-1BB lentiviral vector. The drug candidate is developed by using CAR-T technology.
For a complete picture of Gene Therapy to Target CD19 for Acute Lymphocytic Leukemia and Follicular lymphoma’s drug-specific PTSR and LoA scores, buy the report here.
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GlobalData’s Likelihood of Approval analytics tool dynamically assesses and predicts how likely a drug will move to the next stage in clinical development (PTSR), as well as how likely the drug will be approved (LoA). This is based on a combination of machine learning and a proprietary algorithm to process data points from various databases found on GlobalData’s Pharmaceutical Intelligence Center.
