Gene Therapy for Leukemias is under clinical development by HighPass Bio and currently in Phase I for Chronic Myelocytic Leukemia (CML, Chronic Myeloid Leukemia). According to GlobalData, Phase I drugs for Chronic Myelocytic Leukemia (CML, Chronic Myeloid Leukemia) have a 69% phase transition success rate (PTSR) indication benchmark for progressing into Phase II. GlobalData’s report assesses how Gene Therapy for Leukemias’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 for Leukemias overview
Gene therapy is under development for the treatment of acute leukaemia such as relapsed and refractory acute myeloid leukemia (AML), acute lymphoid leukemia (ALL) and chronic myeloid leukemia (CML) after allogeneic hematopoietic stem cell transplantation. The therapy comprises of T-cells genetically modified by lentiviral transduction to express TCR targeting the leukemia-associated minor H antigen, HA-1 and is administered as an intravenous infusion. It is based on Streptamer technology.
For a complete picture of Gene Therapy for Leukemias’s drug-specific PTSR and LoA scores, buy the report here.