Japan Approves Incyte's Minjuvi Combo for Relapsed or Refractory Follicular Lymphoma

Reuters2025-12-22

Japan Approves Incyte's Minjuvi Combo for Relapsed or Refractory Follicular Lymphoma

Incyte Biosciences Japan has received approval from Japan's Ministry of Health, Labour and Welfare (MHLW) for Minjuvi® (tafasitamab) in combination with rituximab and lenalidomide for the treatment of adult patients with relapsed or refractory follicular lymphoma (2L+ FL). This marks the first regulatory approval for Minjuvi in Japan and represents the first dual-targeted CD19 and CD20 immunotherapy combination for this indication in the country. The approval is based on results from the pivotal Phase 3 inMIND trial, which demonstrated significant improvement in progression-free survival for patients treated with the combination therapy.

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. Incyte Corporation published the original content used to generate this news brief via Business Wire (Ref. ID: 20251221198206) on December 22, 2025, and is solely responsible for the information contained therein.

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