CD19 and CD22 Targeted CAR-T Therapy is under clinical development by Chongqing Precision Biotech and currently in Phase II for Unspecified B-Cell Lymphomas. According to GlobalData, Phase II drugs for Unspecified B-Cell Lymphomas does not have sufficient historical data to build an indication benchmark PTSR for Phase II. GlobalData uses proprietary data and analytics to create drugs-specific PTSR and LoA in the CD19 and CD22 Targeted CAR-T Therapy 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.
CD19 and CD22 Targeted CAR-T Therapy overview
Gene therapy is under development for the treatment of relapsed and refractory B-cell lymphoma, B-cell leukemia and acute lymphocytic leukemia (ALL). It is administered through the intravenous route. The therapeutic candidate comprises of T-cells genetically modified to express chimeric antigen receptor (CAR) that acts by targeting cells expressing CD19 and CD22.
For a complete picture of CD19 and CD22 Targeted CAR-T Therapy’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.
