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Eisai: The Scientific Advisory Group (SAG) to Convene to Discuss the Marketing Authorization Application for lecanemab in the EU -January 11, 2024 at 03:03 am EST

- Eisai Co., Ltd. announced today that the Scientific Advisory Group will convene to discuss the marketing authorization application of lecanemab , which is currently under review by the European...
South Korea United Kingdom Great Britain European Commission Alzheimer Clinical Trial Consortium National Medical Products Administration

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Biogen : "LEQEMBI® Intravenous Infusion" (Lecanemab) for the Treatment of Alzheimer's Disease to be Launched in Japan on December 20 -December 12, 2023 at 09:19 pm EST

TOKYO and CAMBRIDGE, Mass., December 12, 2023 - Eisai Co., Ltd. and Biogen Inc. announced today that humanized anti- soluble aggregated amyloid-beta monoclonal antibody LEQEMBI®...
United Kingdom United States New Zealand Great Britain Christophera Viehbacher Jack Cox

ASTRAZENECA SECURES NHS ACCESS TO IMFINZI▼(DURVALUMAB) IN COMBINATION WITH GEMCITABINE AND CISPLATIN IN ADVANCED BILIARY TRACT CANCER ACROSS ENGLAND A

Imfinzi (durvalumab) in combination with gemcitabine and cisplatin (chemotherapy) has been recommended by the National Institute for Health and Care Excellence (NICE) for the first-line treatment of adults with locally advanced, unresectable, or metastatic biliary tract cancer (BTC).1Durvalumab is AstraZeneca UK&rsq...
United Kingdom City Of Great Britain Helen Morement Ptom Keith Roach David Brocklehurst

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