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CURE Media Group and Oncology Nursing News® announce

Mooney was recognized for her remarkable contributions in oncology care.

Johnson & Johnson's Carvykti Stands Ahead Of Bristol Myers' Rival Blood Cancer Therapy With FDA Approval For Wider Population - Legend Biotech (NASDAQ:LEGN), Johnson & Johnson (NYSE:JNJ)

FDA approves Johnson & Johnson's Carvykti, a BCMA-targeted therapy for relapsed or refractory multiple myeloma patients, offering hope with increased manufacturing capacity and extended collaboration efforts.

Carvykti Approved for Earlier Treatment of Relapsed/Refractory Multiple Myeloma

The approval was based on data from the phase 3 CARTITUDE-4 study. The FDA has approved Carvykti for the treatment of adults with relapsed or refractory multiple myeloma after at least 1 prior lines of therapy.

CARVYKTI® is the First and Only BCMA-Targeted Treatment Approved by the U.S. FDA for Patients with Relapsed or Refractory Multiple Myeloma Who Have Received at Least One Prior Line of Therapy

Johnson & Johnson: CARVYKTI is the First and Only BCMA-Targeted Treatment Approved by the U.S. FDA for Patients with Relapsed or Refractory Multiple Myeloma Who Have Received at Least One Prior Line of Therapy