Anitocabtagene autoleucel is under clinical development by Arcellx and currently in Phase II for Refractory Multiple Myeloma. According to GlobalData, Phase II drugs for Refractory Multiple Myeloma have a 35% phase transition success rate (PTSR) indication benchmark for progressing into Phase III. GlobalData’s report assesses how Anitocabtagene autoleucel’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.
Anitocabtagene autoleucel overview
Anitocabtagene autoleucel is under development for the treatment of relapsed or refractory multiple myeloma. The immune cell therapy consists of Antigen Receptor Complex T cells (ARC-T) T containing a novel synthetic protein1,2 binding domain (non-scFv) that kills the tumor cells. It acts by targeting cells expressing BCMA. It is administered through intravenous route.
Arcellx overview
Arcellx is a clinical-stage biopharmaceutical company that develops, manufactures and markets adaptive cell therapies for treatment of cancer, acute myeloid leukemia, solid tumors and autoimmune diseases. It is headquartered in Gaithersburg, Maryland, the US.
For a complete picture of Anitocabtagene autoleucel’s drug-specific PTSR and LoA scores, buy the report here.
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