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Efficacy and safety of retatrutide for the treatment of obesity: a systematic review of clinical trials.

J Basic Clin Physiol Pharmacol · 2025

Last updated 2026-05-28

In clinical trials involving 691 people with obesity, those given retatrutide lost more weight than those given a placebo. The highest dose tested, 12 mg, led to the greatest reductions in body weight, waist size, and body mass index, with more participants reaching weight loss milestones of 5%, 10%, 15%, or 20%. Side effects were mostly mild stomach issues.

AI summary of the abstract below.

JournalJ Basic Clin Physiol Pharmacol, 2025
Citations0
Molecules retatrutide
Conditions studied Obesity

Abstract

INTRODUCTION: Obesity is a major public health issue linked to various health complications. Retatrutide, a triple agonist peptide targeting the glucagon receptor, GIP receptor, and GLP-1 receptor, shows promise in addressing this need. CONTENT: This systematic review assessed the safety and efficacy of retatrutide for obesity treatment using available clinical trial data. We conducted a comprehensive search of databases, including PubMed, Cochrane and ClinicalTrials.gov, from their inception until March 15, 2025 following PRISMA guidelines. SUMMARY: Three articles were included in this systematic review, screening a total of 1,082 patients, with 691 randomly assigned to groups. The average age of participants was 54.26 ± 9.9 years, consisting of 335 men (48 %) and 356 women (52 %). Retatrutide was administered to 510 participants, while 130 received a placebo. The 12 mg dosage of retatrutide showed the most significant reductions in body weight, body mass index, and waist circumference. It also led to a higher percentage of patients achieving weight losses of ≥5 , 10, 15, and 20 %. Gastrointestinal adverse effects were the most commonly reported. OUTLOOK: Weekly subcutaneous injections of retatrutide in obese patients resulted in significant weight loss and metabolic improvements compared to a placebo.

Verbatim abstract via PubMed 40728138 ↗

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