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Retatrutide

LY3437943, LY-3437943

Quick Stats
Studies 83
Trials 32
Score 4
2025 pubmed 7 citations

Comparative efficacy of incretin drugs on glycemic control, body weight, and blood pressure in adults with overweight or obesity and with/without type 2 diabetes: a systematic review and network meta-analysis.

Liu. Song S; Hu. Jiaqiang J; Zhao. Chen C; Liu. Hang H; He. Chunyang C

Key Findings

  • Retatrutide produced an average weight loss of ~11.9 kg (≈26 lb) compared with placebo.
  • Tirzepatide showed slightly greater weight loss (~12.8 kg) and significantly reduced systolic (‑6.7 mmHg) and diastolic (‑3.7 mmHg) blood pressure.
  • All multi‑receptor agents, including retatrutide, lowered HbA1c by >1% in type‑2‑diabetes patients; tirzepatide and mazdutide had the strongest glycemic effect.
  • Safety analysis found no increase in serious adverse events for any of the agents, with tirzepatide having the most favorable tolerability profile.

Practical Outcomes

  • For biohackers seeking potent weight‑loss tools, retatrutide appears to be a high‑impact option, delivering roughly a 12 kg drop in weight with modest blood‑pressure benefits and a clean safety record. It can be considered alongside tirzepatide, using similar titration schedules, but access is currently limited to clinical trials or specialty pharmacies. Pairing the peptide with a low‑calorie diet and regular exercise will likely maximize results while monitoring for typical GI side‑effects.

Summary

A big review of 24 trials shows that the new multi‑receptor peptide retatrutide can cut about 12 kg (26 lb) off body weight in people who are overweight or obese, and it also lowers blood pressure a bit. Its cousin tirzepatide works just as well or a little better for weight loss and drops systolic pressure by roughly 7 mmHg. Both drugs lower blood sugar by more than 1% in diabetics, and serious side‑effects are rare.

Abstract

The rapid development of multi-receptor drugs targeting glucagon-like peptide-1 receptor (GLP-1R) is driving significant advancements in the treatment of individuals with type 2 diabetes and obesity. This systematic review and network meta-analysis aims to compare the efficacy and safety of multi-receptor drugs in adults with overweight or obesity, with or without type 2 diabetes. A systematic search was conducted in PubMed, Cochrane, Web of Science, Embase, CNKI, and WanFang databases up to May 12, 2024. Randomized controlled trials (RCTs) with an intervention duration of at least 12 weeks were included. The population of interest consisted of individuals with overweight or obesity, with or without type 2 diabetes. Eligible studies compared multi-receptor drugs with placebo or other multi-receptor drugs. The primary outcomes were weight reduction, glycated hemoglobin (HbA<sub>1c</sub>), fasting plasma glucose (FPG), blood pressure changes, and adverse events. Risk of bias was assessed using the version 2 of the Cochrane risk-of-bias tool (ROB2), and a random-effects network meta-analysis was performed using the frequentist approach. Confidence in effect estimates was evaluated using the Confidence In Network Meta-Analysis (CINeMA) framework. A total of 24 trials, involving 9165 participants, were included. Retatrutide (mean difference (MD): -11.91&#xa0;kg, 95% CI: -19.00 to -4.82, P-score: 0.80, p: 0.0003) and Tirzepatide (MD: -12.78&#xa0;kg, 95% CI: -16.10 to -9.46, P-score: 0.89, p &lt; 0.0001) exhibited superior efficacy in reducing body weight, with all other agents except Mazdutide (MD: -5.31&#xa0;kg, 95% CI: -9.78 to -0.84, P-score: 0.37, p: 0.0189) achieving reductions of over 8&#xa0;kg. In patients with type 2 diabetes, all agents reduced HbA<sub>1c</sub> by over 1%, with Tirzepatide (MD: -1.87%, 95% CI: -2.15 to -1.59, P-score: 0.87, p &lt; 0.0001) and Mazdutide (MD: -1.89%, 95% CI: -2.43 to -1.35, P-score: 0.88, p &lt; 0.0001) showing the greatest effects on glycemic control. For blood pressure management, Tirzepatide significantly reduced systolic blood pressure (MD: -6.69 mmHg, 95% CI: -7.62 to -5.75, P-score: 0.84, p &lt; 0.0001) and diastolic blood pressure (MD: -3.73 mmHg, 95% CI: -4.75 to -2.71, P-score: 0.92, p &lt; 0.0001), with nearly all agents lowering systolic blood pressure by more than 5 mmHg. Non-diabetic participants showed more pronounced improvements in both weight and blood pressure. Safety analysis revealed that Tirzepatide had a favorable safety profile and all agents showed no significant impact on serious adverse events compared to placebo. Multi-receptor drugs demonstrated substantial therapeutic potential in weight management, glycemic control, and blood pressure regulation in adults with overweight or obesity, with or without diabetes, with a generally favorable safety profile. https://www.crd.york.ac.uk/prospero/, identifier CRD42024554005.

Study Information

Provider

pubmed

Year

2025

Date

2025-02-04T00:00:00.000Z

DOI

10.3389/fendo.2025.1513641

Citations

7

References

30