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Retatrutide

LY3437943, LY-3437943

Quick Stats
Studies 83
Trials 32
Score 4
2024 pubmed 1 citations

The First Triple Agonist for Antiobesity: Retatrutide.

Tetelbaun. Lauren L; Mullally. Jamie A JA; Frishman. William H WH

Key Findings

  • Retatrutide is a triple‑agonist (GLP‑1R, GIPR, glucagon) that produced greater weight loss than placebo in phase 1/2 trials.
  • Pharmacokinetics are dose‑proportional with a ~6‑day half‑life, supporting convenient once‑weekly dosing.
  • Safety profile mirrors existing GLP‑1 therapies, with gastrointestinal upset being the most common adverse event.

Practical Outcomes

  • For biohackers, retatrutide points to a future weekly injectable that could deliver 10‑15% or more body‑weight loss, far beyond typical diet/exercise results. Until it gains regulatory approval, the best actionable step is to monitor trial updates and consider enrolling in studies if eligible. When available, start with the lowest effective dose to gauge tolerance, then titrate upward as tolerated to maximize weight‑loss benefits.

Summary

Retatrutide is a new experimental drug that hits three hormone receptors (GLP‑1, GIP, and glucagon) and has shown strong weight‑loss results in early‑stage trials. It works with a once‑weekly injection, has a half‑life of about six days, and its side‑effects are mainly stomach‑related, similar to other GLP‑1 drugs. Higher doses gave bigger drops in body weight, suggesting it could become a powerful tool for people looking to lose fat and improve metabolic health once it’s approved.

Abstract

The prevalence of individuals with overweight and obesity has increased by 18% since 1990 and it is projected that by 2030, nearly 50% of US adults will have obesity. Lifestyle modifications, such as diet and exercise, typically lead to approximately 3-5% weight loss, whereas 5-15% weight loss is necessary to significantly impact obesity-associated comorbidities and improve overall health outcomes. In addition to lifestyle modifications, pharmacotherapy has been utilized as an adjunctive treatment to increase weight loss and improve health outcomes. The Food and Drug Administration has currently approved 6 drugs to treat overweight and obesity, with the recently approved drugs surging in popularity after demonstrating superior weight loss outcomes. Additionally, a number of agents are in the pipeline, offering promise of unprecedented degrees of weight loss. One such drug is retatrutide, which is a triple agonist targeting the glucagon-like peptide-1 receptor (GLP-1R), glucose-dependent insulinotropic polypeptide receptor, and glucagon receptor. Phase 1 and 2 clinical trials have demonstrated the safety, tolerability, and pharmacokinetics of retatrutide in patients with obesity and/or type 2 diabetes. The pharmacokinetics of retatrutide were dose proportional and its mean half-life of approximately 6 days supported a once-weekly dosing. The safety profile was similar to GLP-1R agonists and glucose-dependent insulinotropic polypeptide receptor/GLP-1R co-agonists, with gastrointestinal disorders being the most common adverse effects reported. Each trial demonstrated greater weight loss with retatrutide treatment in comparison to placebo, with greatest efficacy at higher doses. Overall, these clinical trials have demonstrated the superior efficacy of retatrutide as a weight loss medication in patients with overweight and obesity.

Study Information

Provider

pubmed

Year

2024

Date

2024-10-08T00:00:00.000Z

DOI

10.1097/crd.0000000000000793

Citations

1

References

17