
FDA Extends Review of Janssen’s CAR T Therapy for Multiple Myeloma
The agency needs more time to review new information on the analytical method used.
The FDA
Cilta-cel is a B-cell maturation antigen (BCMA) chimeric antigen receptor T cell (CAR-T) therapy, is being investigated for the treatment of adults with multiple myeloma. Janssen had
In June 2021, Janssen
Additionally, 66% of patients were progression free and alive at 18 months. The study included patients who had received a median of six prior treatment regimens. Data presented at the American Society of Clinical Oncology Annual Meeting in June 2021 showed an overall survival of 81%.
Both CARTITUDE-1 and the phase 2 CARTITUDE-2 are ongoing.
Cilta-cel was developed by Legend Biotech, and in December 2017, Janssen Biotech entered into a collaboration agreement with Legend Biotech to develop and commercialize cilta-cel.
Multiple myeloma is a cancer that develops in white blood cells. In patients with multiple myeloma, cancer cells accumulate in the bone marrow, crowding out healthy cells. Most patients are diagnosed because of symptoms such as bone fracture or pain, low red blood cell counts, high calcium levels, kidney problems or infections. The American Cancer Society
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