Anti-CD19-CAR is under clinical development by Kecellitics Biotech and currently in Phase I for B-Cell Leukemia. According to GlobalData, Phase I drugs for B-Cell Leukemia have a 71% phase transition success rate (PTSR) indication benchmark for progressing into Phase II. GlobalData’s report assesses how Anti-CD19-CAR’s drug-specific PTSR and Likelihood of Approval (LoA) scores compare to the indication benchmarks. Buy the report here.
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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.
Anti-CD19-CAR overview
Gene therapy is under development for the treatment of B-cell acute lymphocytic leukemia and B-cell leukemia. The therapeutic candidate comprises of autologous T cells expressing chimeric antigen receptor targeting CD19. It acts by targeting B lymphocyte antigen CD19. It is administered through parenteral route.
It was also under development for the treatment of B-cell non-Hodgkin lymphoma.
For a complete picture of Anti-CD19-CAR’s drug-specific PTSR and LoA scores, buy the report here.
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GlobalData, the leading provider of industry intelligence, provided the underlying data, research, and analysis used to produce this article.
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.
