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Retatrutide

LY3437943, LY-3437943

Quick Stats
Studies 83
Trials 32
Score 4
2024 pubmed 200 citations

What is the pipeline for future medications for obesity?

Melson. Eka E; Ashraf. Uzma U; Papamargaritis. Dimitris D; Davies. Melanie J MJ

Key Findings

  • GLP‑1 agonist semaglutide (2.4 mg weekly) yields ~15‑17% average weight loss.
  • Tirzepatide, a GLP‑1/GIP combo, achieves up to 22.5% weight loss in phase‑3 obesity studies.
  • Retatrutide, a GLP‑1/GIP/glucagon triple agonist, is in phase‑3 trials and early results hint at even greater weight loss than tirzepatide.

Practical Outcomes

  • For biohackers, retatrutide represents a potentially powerful future tool for rapid, significant fat loss, but it is not yet available. Keep an eye on upcoming trial results and regulatory updates; when approved, dosing will likely follow a weekly subcutaneous injection similar to other GLP‑1 analogues. Meanwhile, current best practice remains using approved GLP‑1 agents (e.g., semaglutide) and lifestyle measures while monitoring the pipeline for breakthrough options.

Summary

The abstract reviews new obesity drugs that combine gut hormones. The newest triple‑hormone combo, retatrutide (GLP‑1, GIP, and glucagon), is in phase‑3 trials and early data suggest it could cause more weight loss than the current best drug, tirzepatide, possibly approaching the results of bariatric surgery.

Abstract

Obesity is a chronic disease associated with increased risk of obesity-related complications and mortality. Our better understanding of the weight regulation mechanisms and the role of gut-brain axis on appetite has led to the development of safe and effective entero-pancreatic hormone-based treatments for obesity such as glucagon-like peptide-1 (GLP-1) receptor agonists (RA). Semaglutide 2.4 mg once weekly, a subcutaneously administered GLP-1 RA approved for obesity treatment in 2021, results in 15-17% mean weight loss (WL) with evidence of cardioprotection. Oral GLP-1 RA are also under development and early data shows similar WL efficacy to semaglutide 2.4 mg. Looking to the next generation of obesity treatments, combinations of GLP-1 with other entero-pancreatic hormones with complementary actions and/or synergistic potential (such as glucose-dependent insulinotropic polypeptide (GIP), glucagon, and amylin) are under investigation to enhance the WL and cardiometabolic benefits of GLP-1 RA. Tirzepatide, a dual GLP-1/GIP receptor agonist has been approved for glycaemic control in type 2 diabetes as well as for obesity management leading in up to 22.5% WL in phase 3 obesity trials. Other combinations of entero-pancreatic hormones including cagrisema (GLP-1/amylin RA) and the triple agonist retatrutide (GLP-1/GIP/glucagon RA) have also progressed to phase 3 trials as obesity treatments and early data suggests that may lead to even greater WL than tirzepatide. Additionally, agents with different mechanisms of action to entero-pancreatic hormones (e.g. bimagrumab) may improve the body composition during WL and are in early phase clinical trials. We are in a new era for obesity pharmacotherapy where combinations of entero-pancreatic hormones approach the WL achieved with bariatric surgery. In this review, we present the efficacy and safety data for the pipeline of obesity pharmacotherapies with a focus on entero-pancreatic hormone-based treatments and we consider the clinical implications and challenges that the new era in obesity management may bring.

Study Information

Provider

pubmed

Year

2024

Date

2024-02-01T00:00:00.000Z

DOI

10.1038/s41366-024-01473-y

Citations

200

References

117