FDA Approves EPKINLY Plus R2 for Relapsed or Refractory Follicular Lymphoma

Reuters12-07 20:50

FDA Approves EPKINLY Plus R2 for Relapsed or Refractory Follicular Lymphoma

The U.S. Food and Drug Administration (FDA) has approved the combination of EPKINLY® (epcoritamab-bysp) with rituximab and lenalidomide (R2) for the treatment of patients with relapsed or refractory follicular lymphoma (FL) after one or more lines of systemic therapy. This approval makes EPKINLY + R2 the first and only bispecific-based therapy available for FL in the second-line setting. EPKINLY is also approved in the U.S. for adults with relapsed/refractory FL after two or more prior treatments.

Disclaimer: This news brief was created by Public Technologies (PUBT) using generative artificial intelligence. While PUBT strives to provide accurate and timely information, this AI-generated content is for informational purposes only and should not be interpreted as financial, investment, or legal advice. Genmab A/S published the original content used to generate this news brief via GlobeNewswire (Ref. ID: GNW1001143455-en) on December 07, 2025, and is solely responsible for the information contained therein.

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