Senl-h19 is under clinical development by Hebei Senlang Biotechnology and currently in Phase II for B-Cell Acute Lymphocytic Leukemia (B-Cell Acute Lymphoblastic Leukaemia). According to GlobalData, Phase II drugs for B-Cell Acute Lymphocytic Leukemia (B-Cell Acute Lymphoblastic Leukaemia) have a 57% phase transition success rate (PTSR) indication benchmark for progressing into Phase III. GlobalData’s report assesses how Senl-h19’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 is under development for the treatment of relapsed and refractory acute lymphocytic leukemia (ALL). It is administered through parenteral route. The therapeutic candidate constitutes T cells modified to express chimeric antigen receptors (CAR) targeting cells expressing CD19.
Hebei Senlang Biotechnology overview
Hebei Senlang Biotechnology is a pharamaceutial and healthcare company which is involved in using bio technology for treatment of immune cells. The company is headquartered in Dongguan, Hebei, China.
For a complete picture of Senl-h19’s drug-specific PTSR and LoA scores, buy the report here.