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FDA Approves Amgen s RIABNI™ (rituximab-arrx), A Biosimilar To Rituxan® (rituximab)

Share this article Share this article THOUSAND OAKS, Calif., Dec. 17, 2020 /PRNewswire/ Amgen (NASDAQ:AMGN) today announced that the U.S. Food and Drug Administration (FDA) has approved RIABNI™ (rituximab-arrx), a biosimilar to Rituxan ® (rituximab), for the treatment of adult patients with Non-Hodgkin s Lymphoma (NHL), Chronic Lymphocytic Leukemia (CLL), Granulomatosis with Polyangiitis (GPA) (Wegener s Granulomatosis), and Microscopic Polyangiitis (MPA). RIABNI will be made available in the U.S. in January 2021. The approval of RIABNI represents an important milestone across our biosimilar and oncology portfolios, said Murdo Gordon, executive vice president of Global Commercial Operations at Amgen. Following the proven success of KANJINTI

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Mercy releases NWA COVID-19 update | 5newsonline com

Northwest Arkansas hospitals hopeful about COVID-19 vaccine, give update on hospital space Hospital leaders in Northwest Arkansas are hopeful about the vaccine but say the number of COVID-19 cases and hospitalizations continues to be on the rise. Author: 5NEWS Web Staff Updated: 4:30 AM CST December 16, 2020 ROGERS, Arkansas On Monday (Dec. 14), a Northwest Arkansas council provided the following information on behalf of the Northwest Arkansas health care community, to help inform and educate the region. Northwest Arkansas hospitals are hopeful about the vaccine but say the number of COVID-19 cases and hospitalizations continues to be on the rise. As of Dec. 14, 107 patients are in NWA hospital COVID units.

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Global Healthcare Information Exchange Market 2020 Key Performance, Top Players, Segmentation, Future Plans and Forecast to 2025

Global Healthcare Information Exchange Market 2020 Key Performance, Top Players, Segmentation, Future Plans and Forecast to 2025
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