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Study 22 of 23Retatrutide (LY3437943) literatureNature metabolism · PreclinicalTop journal2026

Cagrilintide and retatrutide combination therapy enhances weight loss and metabolic outcomes in obese male rats.

The combination of retatrutide and cagrilintide shows promise for enhancing weight loss and metabolic outcomes in a rodent model, but further research is needed to determine its relevance to human obesity treatment.

Read at Nature metabolismAdd to compare

Where it sits

this study against the rest of the retatrutide (ly3437943) corpus
9
Preclinical · this one
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Observational
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Open-label
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Randomised
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Reviews

Summary and findings

This study investigated the effects of a combination therapy of retatrutide and cagrilintide on weight loss and metabolic outcomes in diet-induced obese male rats. The findings indicated that the combination therapy led to reductions in body weight and improvements in metabolic markers. No therapeutic claims are made regarding human applications.

How much of this paper we could read: partial text (0.60). We had some abstract detail. Check the source for anything decisive. What this means →
Not reported in abstract.Preclinical2026

Abstract

The authors’ words, as Nature metabolism supplied them

Peptide multi-receptor agonists have advanced obesity treatment, yet challenges remain in achieving maximal weight loss and metabolic control, especially in patients with obesity and type 2 diabetes. Here we demonstrate enhanced metabolic benefits of a combination therapy with retatrutide, a unimolecular GLP-1R/GIPR/GCGR tri-agonist, and cagrilintide, an AMLNR/CALCR co-agonist, in diet-induced obese male rats. Daily co-administration produces dose-dependent reductions in body weight and food intake that exceed both equimolar monotherapies and matched-dose comparator combinations incorporating semaglutide or tirzepatide. The combination therapy also improves circulating markers of metabolic health, including cholesterol, triglycerides and insulin levels. Pair-feeding and weight-matching studies reveal that the enhanced weight loss cannot be explained by reduced food intake alone and enable discrimination between weight-loss-dependent and drug-specific molecular responses. Plasma proteomic profiling highlights enrichment of bioenergetic processes with the combination therapy, whereas brain transcriptomic profiling identifies convergent central neuronal programmes linked to energy balance regulation. Collectively, our preclinical findings support five-receptor polypharmacology as a strategy for efficaciously lowering body weight and provide guidance for the design of next-generation unimolecular multi-receptor agonists.

Background

Not reported in abstract.

Methods

Not reported in abstract.

Results

Not reported in abstract.

Interpretation

Not reported in abstract.

Limitations

Not reported in abstract.

Elsewhere in the Retatrutide (LY3437943) corpus

BSustained weight loss exceeding 100 kg with sequential incretin-based therapy in Prader-Willi syndrome.JCEM case reports · 2026 · n=1 · Total weight loss of 58.8% (-108.7 kg) at 18 months.HumanDObstructive sleep apnea, GLP-1 receptor agonist pharmacotherapy, and the oral microbiome: competing biological influences and implications for oral health monitoring.Clinical oral investigations · 2024 · Not reported in abstract.reviewCCagrilintide and retatrutide combination therapy enhances weight loss and metabolic outcomes in obese male rats.Nature metabolism · 2026 · Not reported in abstract.AnimalBDetection and Excretion Profile of Retatrutide in Human Plasma and Urine by LC-HRMS: Implications for Antidoping Analysis.Rapid communications in mass spectrometry : RCM · 2023 · n=4 · Limits of detection (LOD) were 6.14 ng/mL in plasma and 2.44 ng/mL in urine.HumanBDetection and Excretion Profile of Retatrutide in Human Plasma and Urine by LC-HRMS: Implications for Antidoping Analysis.Rapid communications in mass spectrometry : RCM · 2023 · n=4 · Limits of detection in plasma were 6.14 ng/mL and in urine were 2.44 ng/mL.HumanDCARDIOVASCULAR EFFECTS OF INCRETIN RECEPTOR AGONISTS: BEYOND GLYCEMIC CONTROL.Canadian journal of physiology and pharmacology · 2026 · Glycemic improvement accounts for less than 15 to 20 percent of the reduction in major adverse cardiovascular events.review