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Novo Nordisk indicates that the United States FDA approved an additional indication for its Wegovy. Furthermore, for the treatment of the Mash (Steatohepatitis associated with non-cirrhotic metabolic dysfunction).
This approval concerns adults with moderate to advanced liver fibrosis (compatible with fibrosis of F2 to F3 stages). For example, in combination with a hypocaloric diet and increased physical activity.
Petrol clinical data showed that week, 36.8% of people treated by Wegovy obtained an improvement in liver fibrosis without aggravation of steatohepatitis, compared to 22.4% treated with a placebo.
Also according to part 1 of this phase 3 test, the Danish laboratory says that 62.9% of people treated by Wegovy resolved steatohepatitis without worsening hepatic fibrosis, compared to 34.3% with placebo.
Severe. progressive metabolic disease affecting the liver. potentially fatal. the Mash affects more than 250 million novo nordisk: fda green light new people. the number novo nordisk: fda green light new of novo nordisk: fda green light new novo nordisk: fda green. light new people at advanced stages. of the disease should novo nordisk: fda green light double novo nordisk: fda green light by 2030.
novo nordisk: fda green light — Novo nordisk: fda green light: Novo Nordisk indicates that the United States. FDA approved an additional indication for its Wegovy. for the treatment of the Mash (Steatohepatitis associated with non-cirrhotic metabolic dysfunction).This approval concerns adul.
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novo nordisk: fda novo nordisk: fda green light new green light — Meanwhile. Novo nordisk: novo nordisk: fda green light new fda green light: Novo Nordisk indicates that the United States FDA. approved an novo nordisk: fda green. light additional indication for its Wegovy. Furthermore, for the treatment of the Mash (Steatohepatitis associated with non-cirrhotic metabolic dysfunction).This approval concerns a.
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