Dark Mode Light Mode
The doctor says that all women should be able to do this difficult exercise.
If the FDA is approved, the FDA accepts the application for 25 mg of oral semagluide, which will be the first oral GLP-1 treatment for obesity.
How the climate change worsens

If the FDA is approved, the FDA accepts the application for 25 mg of oral semagluide, which will be the first oral GLP-1 treatment for obesity.

Spread the love


  • NOVO NORDISK hopes to expand Wegovy® It becomes the first and attaches the label GLP-1 Pill

  • The FDA submission is based on the results of the 3 -phase Oasis 4 exam, which evaluated 25 mg of oral cavity and overweight adults who are obese or overweight.1

  • NOVO NORDISK continues to build more than 100 years of legacy of science and innovation.

Plain Boro, New Jersey,,, May 2, 2025 / Prnewswire/-Today, Novo Nordisk has announced that the US Food and Drug Administration (FDA) has accepted a new drug application (NDA) for once a day.® (Semaglutide) Reduces the risk of major side effects of the adults with one or more accompanying diseases for chronic weight management of obesity or overweight adults.2 WEGOVY for approval® It will be the first oral formulation of A GLP-1 It is displayed for chronic weight management.

Novo Nordisk, Inc. (Prnewsfoto/Novo Nordisk)
Novo Nordisk, Inc. (Prnewsfoto/Novo Nordisk)

Anna Windle, vice president of clinical development and vice president of medical and regulations at Novo Nordisk Inc., said, “We are planning a new obesity treatment plan that wants patients to solve their own needs and provide individualized treatment plans that provide choices including oral formulations. GLP-1 Obesity treatment. “

FDA applications are based on the results of Oasis 4, a 64 -week 3 -phase control test that assesses the efficacy and safety of 25 mg of oral semi -glute on 307 people with obesity (BMI>/= 30 kg/m.2) Or overweight (bmi>/= 27 kg/m2) One or more accompanying diseases.1,3 Diabetes were excluded.1,3

Oasis 4 includes a 12 -week dose escalation and a 64 -week processing period, including the after treatment period after treatment for 7 weeks.1,3 A total of 307 participants were randomly assigned at a 2: 1 ratio for 25 mg of oral semagluide or placebo for 64 weeks.1,3

The FDA measure date determines Wegovy® The oral formulation NDA will be in the fourth quarter of 2025.2

About Wegovy®
Wegovy® (SEMAGLUTIDE) Injection 2.4 mg is currently in some adults with adults over 12 years of age and adults and children, children or weight -related medical problems in adults, children, or weight -related problems in the case of adults and physical problems. It helps to take or deliberately look at it.4





Source link

Keep Up to Date with the Most Important News

By pressing the Subscribe button, you confirm that you have read and are agreeing to our Privacy Policy and Terms of Use
Add a comment Add a comment

Leave a Reply

Your email address will not be published. Required fields are marked *

Previous Post

The doctor says that all women should be able to do this difficult exercise.

Next Post

How the climate change worsens