CD19 Targeted CAR-T Therapy is under clinical development by Chongqing Precision Biotech and currently in Phase I for Dermatomyositis. According to GlobalData, Phase I drugs for Dermatomyositis have a 91% phase transition success rate (PTSR) indication benchmark for progressing into Phase II. GlobalData’s report assesses how CD19 Targeted CAR-T Therapy’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.
CD19 Targeted CAR-T Therapy overview
The therapeutic candidate is under development for the treatment of refractory systemic lupus erythematosus, systemic scleroderma, Sjogren's syndrome, dermatomyositis and anti-neutrophil cytoplasmic antibody associated vasculitis (ANCA-AAV), including granulomatosis with polyangiitis (GPA), or microscopic vasculitis (MPA), or eosinophilic granulomatosis with polyangiitis (EGPA). It comprises of T-cells genetically engineered to express chimeric antigen receptors (CAR) targeting cell expressing CD19 and is administered through intravenous route.
For a complete picture of CD19 Targeted CAR-T Therapy’s drug-specific PTSR and LoA scores, buy the report here.
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