Incyte Japan announces approval of Minjuvi for DLBCL
The combination with lenalidomide was approved by Japan's MHLW for relapsed or refractory diffuse large B-cell lymphoma.
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Global biopharmaceutical company
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In short: Incyte reported strong 2026 financial growth, secured FDA approval for Jakafi XR, and advanced its pipeline through several key drug acquisitions.
The combination with lenalidomide was approved by Japan's MHLW for relapsed or refractory diffuse large B-cell lymphoma.
The PROGRESS study showed reduced heterotopic ossification and FDA accepted NDA under Priority Review.
The Tafa-Len-R-CHOP regimen reduced risk of disease progression or death by 25% compared to R-CHOP. Data presented at EHA 2026 Congress.
The drug achieved rapid, robust clinical and molecular responses and was well tolerated in MF and ET patients.
Incyte ( (INCY)) has issued an update. Incyte Corporation has reached an agreement with the Centers for Medicare & Medicaid Services to resolve litigation over...
WILMINGTON, DE — Incyte (Nasdaq: INCY) reported Phase III trial results showing that adding tafasitamab and lenalidomide to the standard R-CHOP regimen reduced the risk...
Incyte Biosciences Japan G.K. today announced that Japan’s Ministry of Health, Labour and Welfare (MHLW) has approved Minjuvi ® (tafasitamab) in combination with lenalidomide for...
Incyte shares stay in focus on Nasdaq as investors weigh fresh clinical trial results, a recent S&P 500 swing and updated long-term revenue projections while...
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