Swiss drug major Roche (RHHBY) announced Thursday positive results from the Phase I clinical trial of its dual GLP-1/GIP receptor agonist CT-388 being developed for the treatment of obesity and type 2 diabetes.
Roche announced today that the European Medicines Agency s Committee for Medicinal Products for Human Use has recommended approval of Alecensa as monotherapy, as adjuvant therapy in patients with.
19.04.2024 - Approval based on Phase III ALINA study showing Alecensa reduced the risk of disease recurrence or death by an unprecedented 76% in people with ALK-positive early-stage resected non-small cell lung cancer (NSCLC)1This approval helps address an . Seite 1
F Hoffmann-La Roche Ltd: FDA approves Roche s Alecensa as the first adjuvant treatment for people with ALK-positive early-stage lung cancer finanznachrichten.de - get the latest breaking news, showbiz & celebrity photos, sport news & rumours, viral videos and top stories from finanznachrichten.de Daily Mail and Mail on Sunday newspapers.
Approval based on Phase III ALINA study showing Alecensa reduced the risk of disease recurrence or death by an unprecedented 76% in people with ALK-positive early-stage resected non-small cell lung.