With a new endorsement from the FDA, Novo Nordisk’s Wegovy has picked up its third indication and become the second drug ...

The approval makes Wegovy the only GLP-1 therapy cleared to treat adults with metabolic dysfunction-associated ...

Novo Nordisk's blockbuster weight-loss drug, Wegovy, received Food and Drug Administration approval to treat a serious ...

Novo Nordisk said on Friday the U.S. Food and Drug Administration has granted accelerated approval for its weight-loss drug ...

The label expansion could help Novo Nordisk “help shift the momentum” for Wegovy, after a difficult start to 2025, according ...

Wegovy is now approved by the FDA to treat metabolic-associated steatohepatitis in adults with moderate-to-advanced fibrosis ...

Wegovy is now the second medicine approved in the U.S. for a disease that affects millions. Novo Nordisk has several other factors working in its favor, including strong results and a solid pipeline.

ノボ・ノルディスクのFDA承認は、第3相ESSENCE試験の結果に基づいており、Wegovyで治療を受けた患者の63%が肝線維症の悪化なしに脂肪性肝炎の改善を達成したのに対し、プラセボでは34%であった。さらに、Wegovyで治療を受けた患者の37% ...

Wegovyは、MASHに対して承認された初のGLP-1ベースの治療薬となる。米国肝臓財団によると、MASHは米国成人の約5%が罹患している。これまで、この疾患に対するFDA承認済みの治療薬は、2024年に承認された Madrigal ...

Novo Nordisk's Wegovy has received accelerated approval for use in patients with metabolic dysfunction-associated ...

The FDA clearance sets Novo’s medicine up a market battle with Madrigal Pharmaceuticals’ fast-selling Rezdiffra.

FDA has approved Novo Nordisk's Wegovy, one-weekly 2.4 mg semaglutide injection for treating metabolic-associated ...