SEMAGLUTIDE

SEMAGLUTIDE 

Semaglutide works by mimicking a hormone called glucagon (similar to peptide-1 GLP-1) that targets areas of the brain that regulate appetite and food intake. 

Semaglutide safety and efficacy were studied in four 68-week trials. Three were randomized, double-blind, placebo-controlled trials (including 16 weeks of dose increases) and one was a double-blind, placebo-controlled, randomized withdrawal trial.

Patients receiving Semaglutide either continued with the treatment or switched to a placebo. More than 2,600 patients received Semaglutide for up to 68 weeks in these four studies and more than 1,500 patients received placebo.

The largest placebo-controlled trial enrolled adults without diabetes. The average age at the start of the trial was 46 years and 74% of patients were female.

The average body weight was 231 pounds (105 kg) and average BMI was 38 kg/m2.

Individuals who received Semaglutide lost an average of 12.4% of their initial body weight compared to individuals who received placebo.

Another trial enrolled adults with type 2 diabetes. The average age was 55 years and 51% were female. The average body weight was 220 pounds (100 kg) and average BMI was 36 kg/m2.

In this trial, individuals who received Semaglutide lost 6.2% of their initial body weight compared to those who received placebo.