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Wegovy (semaglutide 2.4 mg) approved in the US for the treatment of MASH Novo Nordisk Novo Nordisk announced that the FDA has approved an additional indication for Wegovy (semaglutide 2.4 mg) based on a supplemental New Drug Application (sNDA) for treatment of noncirrhotic metabolic dysfunction-associated steatohepatitis (MASH) in adults with moderate to advanced liver fibrosis (consistent with stages F2 to F3 fibrosis), in combination with a reduced calorie diet and increased physical activity

District Judge Karen Spencer Marston partially granted and partially denied several key motions, clarifying how scientific and legal questions will be handled moving forward

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They help protect the skin from damage caused by free radicals, which can lead to premature aging and uneven skin tone

They may prevent type 2 diabetes progression or even induce remission in early-stage cases

Key Takeaways MT1 (afamelanotide) is FDA-approved (2019) and EMA-approved (2014) for erythropoietic protoporphyria under the brand name Scenesse