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The Current Role of Liraglutide in the Pharmacotherapy of Obesity.

Curr Vasc Pharmacol · 2016

Last updated 2026-05-28

Liraglutide at a 3.0 mg daily dose led to a 5.9–8.0% weight reduction over 56 weeks, compared to a 3.9–6.0% reduction with placebo. About 50–76% of patients lost at least 5% of their body weight with liraglutide, versus 29–46% with placebo. The treatment also lowered waist size, blood fats, insulin resistance, and blood pressure, while raising HDL cholesterol. Common side effects included nausea, low blood sugar, diarrhea, constipation, vomiting, and headache.

AI summary of the abstract below.

JournalCurr Vasc Pharmacol, 2016
Citations16
Relative citation ratio0.65
NIH percentile36
Molecules liraglutide
Conditions studied Obesity

Abstract

OBJECTIVE: Liraglutide 3.0 mg daily dose is marketed under the brand name Saxenda and was recently approved by both the Food and Drug Administration (FDA) and the European Medicine Agency (EMA) as adjunct to a comprehensive lifestyle intervention to achieve weight loss. DESIGN: Human studies using liraglutide 3.0 mg daily dose were selected through search based on PubMed listings and the Clinical trials.gov database using the term "liraglutide". RESULTS: During 56 weeks of treatment, liraglutide 3.0 mg treatment resulted in 5.9-8.0% weight reduction, while the placebo-subtracted weight loss was 3.9-6.0%. The proportion of treated patients with ≥ 5% weight loss was 50-76%, while the placebo-subtracted proportion was 29-46%. Liraglutide 3.0 mg treatment also induced a decrease in waist circumference, serum triglycerides, insulin resistance, blood pressure and an increase in high density lipoprotein-cholesterol (HDL-C). The most common side effects were nausea, hypoglycemia, diarrhea, constipation, vomiting and headache. In the majority of patients liraglutide 3.0 mg was well tolerated. CONCLUSION: Liraglutide 3.0 mg appears to be an effective adjunct to a comprehensive lifestyle intervention to achieve weight reduction and treat obesity-related comorbidities.

Verbatim abstract via PubMed 26074046 ↗

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