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-0.000148780956037656 -0.000863889422153997 -0.00383950854290656 -0.00403148397005185 0.00239969283931657 0.00964676521405256 0.0253455557688616 0.0191975427145325
Stock impact report

INCY's Phase III Monjuvi Study Meets Key Goals in First-Line Lymphoma [Yahoo! Finance]

Incyte Corporation (INCY) 
Last incyte corporation earnings: 2/13 07:00 am Check Earnings Report
US:NASDAQ Investor Relations: incyte.com/ir/investor-overview.aspx
Company Research Source: Yahoo! Finance
The drug, in combination with Bristol Myers ' BMY Revlimid (lenalidomide), is approved in the United States and the EU under the brand names Monjuvi and Minjuvi, respectively, for the treatment of adult patients with relapsed or refractory diffuse large B-cell lymphoma (DLBCL). The eligible patient population included cases arising from low-grade lymphoma, who are ineligible for autologous stem cell transplant. More recently, the FDA approved Incyte's Monjuvi in combination with BMY's Revlimid and Roche's Rituxan (rituximab) in mid-2025 for adult patients with relapsed or refractory follicular lymphoma (FL). Last month, the regulatory body in the EU also approved the label expansion of Minjuvi for patients with relapsed or refractory FL, further expanding its presence across hematologic malignancies. Incyte's pivotal phase III frontMIND study evaluating the efficacy and safety of Monjuvi/Minjuvi and Bristol Myers' Revlimid in combination with R-CHOP (Rituxan, cyclophosphamide, do Show less Read more
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