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GSK first with FDA approved treatment for blood cancer and anemia


The small molecule drug Ojjaara (momelotinib), developed by GlaxoSmithKline, has become the first U.S. Food and Drug Administration (FDA)-approved treatment for patients with the blood cancer myelofibrosis and anemia. ....

Nina Mojas , Clinical Development , Pis Active Pharmaceutical Ingredients , Delivery Formulations , Blood Cancer Drug ,

Ojjaara Approved for Intermediate or High-Risk Myelofibrosis With Anemia

Ojjaara Approved for Intermediate or High-Risk Myelofibrosis With Anemia
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Nina Mojas , Drug Administration , Senior Vice President , Oncology Global Product Strategy ,

FDA Approves Momelotinib for Myelofibrosis With Anemia

The agency's approval of momelotinib marks the first for both newly diagnosed and previously treated myelofibrosis with anemia. ....

Nina Mojas , Rubena Mesa , Atrium Health Levine Cancer Center , Olivier Le Moal , Updated August , Momelotinib Fda Approval ,

Ojjaara (momelotinib) approved in the US as the first and only treatment indicated for myelofibrosis patients with anemia

16.09.2023 - GSK plc (LSE/NYSE: GSK) today announced that the US Food and Drug Administration (FDA) has approved Ojjaara (momelotinib) for the treatment of intermediate or high-risk myelofibrosis, including primary myelofibrosis or secondary myelofibrosis . Seite 1 ....

Nina Mojas , Drug Administration , Senior Vice President , Oncology Global Product Strategy , Gsk Chart , Sk Kurs , Sk Aktie ,