Trials & Filings

FDA Approves Legend, Janssen CAR-T Therapy for Multiple Myeloma

Phase 1b/2 study demonstrates overall response rate of 98% in patients with refractory or relapsed multiple myeloma after four or more prior lines of therapy.

Author Image

By: Kristin Brooks

Managing Editor, Contract Pharma

Legend Biotech Corp., a global biotechnology company developing novel therapies to treat life-threatening diseases, received its first approval from the U.S. FDA for CARVYKTI (ciltacabtagene autoleucel; cilta- cel), for the treatment of adults with relapsed or refractory multiple myeloma (RRMM) who have received four or more prior lines of therapy, including a proteasome inhibitor, an immunomodulatory agent, and an anti-CD38 monoclonal antibody. Legend Biotech entered into an exclusive worldwide...

Continue reading this story and get 24/7 access to Contract Pharma for FREE


Already a subscriber? Sign in

Keep Up With Our Content. Subscribe To Contract Pharma Newsletters