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Hutchmed's sovleplenib meets primary, secondary endpoints in China phase III ITP trial

Hutchmed (China) Ltd.’s sovleplenib (HMPL-523) met the primary endpoint of durable response rate and all secondary endpoints in the pivotal phase III trial in adults with primary immune thrombocytopenia (ITP) in China. ....

Hutchmed China Ltd , Hutchmed China Ltd , Hmpl 523 , Primary Immune Thrombocytopenia , Warm Antibody Autoimmune Hemolytic Anemia , Indolent Non Hodgkin Lymphoma ,

Fruquintinib significantly improves survival in patients with refractory metastatic colorectal cancer

1. Overall survival was significantly greater in the fruquintinib group versus placebo. 2. The majority of adverse events were mild-to-moderate and were slightly more common among patients receiving fruquintinib. Evidence Rating Level: 1 (Excellent) Study Rundown: Colorectal cancer is the third-most prevalent cancer in the world and the second leading cause of death worldwide. Patients ....

Rating Level , Colonoscopy Screening , Colorectal Cancer , Between Aug , Colon Cancer , Metastatic Colorectal Cancer , Vegf Inhibitors , Chronic Disease ,

European Medicines Agency Validates MAA for Fruquintinib in Pretreated mCRC

The European Medicines Agency has validated and accepted a marketing authorization application for priority review for fruquintinib for the treatment of adult patients with pretreated metastatic colorectal cancer. ....

United States , Michael Shi , European Union , European Medicines Agency , Prescription Drug User Fee Act , Marketing Authorization Application , European Medicines , European Union Eu , Colorectal Cancer , European Medicines Agency ,