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Leqembi® Iqlik™ (lecanemab-irmb) supplemental Biologics License Application regarding subcutaneous starting dose granted Priority Review by the US FDA

PR Newswire

Les revendications de brevet soulevées par Tulip Innovation contre les batteries Sunwoda s'étendent à l'action de la Korea Trade Commission (Commission coréenne du commerce - KTC)

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Ascletis Announces First Participants Dosed in a 13-week U.S. Phase II Study with ASC30, an Oral Small Molecule GLP-1R Agonist for the Treatment of Diabetes

PR Newswire

Lee Kum Kee zahajuje ve spolupráci s UNESCO „Forever Flavors Project" s cílem vybudovat světový archiv kulinářských vzpomínek

PR Newswire

Argo Biopharma Announces First Patient Dosed in Phase 2b Trial of siRNA Therapeutic BW-20829 in Patients with Elevated Lp(a)

PR Newswire

FDA Accepts LEQEMBI® IQLIKTM (lecanemab-irmb) Supplemental Biologics License Application as a Subcutaneous Starting Dose for the Treatment of Early Alzheimer's Disease under Priority Review