Incyte Corporation Announces FDA Approval of Monjuvi® Combination Therapy for Relapsed or Refractory Follicular Lymphoma

Reuters

06-19

Incyte Corporation Announces FDA Approval of Monjuvi® Combination Therapy for Relapsed or Refractory Follicular Lymphoma

Incyte Corporation has announced that the U.S. Food and Drug Administration (FDA) has granted approval for Monjuvi® (tafasitamab-cxix), in combination with rituximab and lenalidomide, for the treatment of adult patients with relapsed or refractory follicular lymphoma $(FL)$. This marks the second approved indication for Monjuvi in the United States. The approval comes as a significant development for patients with relapsed or refractory FL, offering a new option that targets CD19 and CD20 with an immunotherapy combination. Incyte is committed to supporting patients through IncyteCARES, a program that provides personalized support, including financial assistance and educational resources.

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: 20250615896694) on June 18, 2025, and is solely responsible for the information contained therein.

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ID: 20250615896694) on June 18, 2025, and is solely responsible for the information contained therein.</span></em>\n</div></body></html>\n</article>\n</div>\n</body>\n</html>\n","isBrief":false,"type":0,"news_type":1,"symbol":null,"symbol_name":null,"start_time":0,"source_url":"https://api.refinitiv.com/data/news/v1/stories/urn:newsml:reuters.com:20250618:nNDL7yvX7n:1","article_id":"2544900848","we_media_id":"1032215980","thumbnails":[],"rights":null,"url":"https://stock-news.laohu8.com/highlight/detail?id=2544900848","pubTimestamp":1750275558,"columns":[],"sourceInfo":null,"weMediaInfo":{"media_name":"Reuters","introduction":"Reuters.com brings you the latest news from around the world, covering breaking news in markets, business, politics, entertainment and technology","home_visible":1,"id":"1032215980","head_image":"https://community-static.tradeup.com/news/4567337cbdf294b657b1fa87c5488b48"},"summary":"Incyte Corporation has announced that the U.S. Food and Drug Administration  has granted approval for Monjuvi , in combination with rituximab and lenalidomide, for the treatment of adult patients with relapsed or refractory follicular lymphoma . 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