Gene Therapy to Target CD19 for Hematological Tumors is under clinical development by Chengdu USino Technology Biology and currently in Phase I for Hematological Tumor. According to GlobalData, Phase I drugs for Hematological Tumor does not have sufficient historical data to build an indication benchmark PTSR for Phase I. GlobalData uses proprietary data and analytics to create drugs-specific PTSR and LoA in the Gene Therapy to Target CD19 for Hematological Tumors LoA Report. 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 Hematological Tumors overview
Gene therapy is under development for the treatment of relapsed/refractory hematologic malignancies, including CD19 positive B-cell acute lymphoblastic leukemia (B-ALL), B-cell chronic lymphoblastic leukemia (B-CLL), and B-cell lymphoma. It is administered through parenteral route. The therapeutic candidate (CAR-NK) comprises genetically modified cord blood derived T cells from healthy donor, expressing chimeric antigen receptors (CAR) targeting cells expressing CD19 (universal anti-CD19 CAR-modified AT19 cells).
For a complete picture of Gene Therapy to Target CD19 for Hematological Tumors’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.
