Reta + Tesamorelin Blend, product photo
GLP-1

Reta + Tesamorelin Blend

Injectable blend of the triple-incretin agonist Retatrutide and the GHRH analog Tesamorelin. Metabolic action meets the GH axis in a single vial.

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At a glance

Reta + Tesamorelin Blend by the numbers

The key figures from our lexicon.

Full lexicon entry
Type
Injectable blend

triple agonist + GHRH analog

Sizes
20 mg

1 size in the shop

For research and educational purposes only. Values from the TPD lexicon, sources linked there.

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Knowledge

Everything about Reta + Tesamorelin Blend

Description

This blend combines two research compounds from different classes in a single injectable vial. One is Retatrutide (LY3437943), a triple-incretin agonist that simultaneously activates GLP-1, GIP and glucagon receptors. The other is Tesamorelin, a synthetic analog of growth-hormone-releasing hormone (GHRH). Retatrutide addresses the incretin axis across three receptor systems at once, with the glucagon component associated in research with increased energy expenditure and greater lipid breakdown. Tesamorelin acts at an entirely different site: as a selective agonist at the GHRH receptor of the pituitary, stimulating the body’s own pulsatile growth hormone release rather than supplying GH directly.

Both active ingredients are injectable peptides in their clinically studied form. That is exactly how this blend ships: as a freeze-dried powder (lyophilizate) that you reconstitute with bacteriostatic water and administer subcutaneously. This matches the route on which the published studies are based. What still needs framing honestly: there are no robust clinical data on precisely this Reta-plus-Tesamorelin combination in one vial. The evidence stems from the individual compounds. The two have very different dosing magnitudes, which makes the fixed 1:1 mix experimental.

The core research findings stem from the injectable individual compounds. For Retatrutide, phase 2 data showed body weight reductions of up to 24.2 percent after 48 weeks in study models with subjects who had obesity. They also showed reductions in liver fat content in MASLD research. For Tesamorelin, pooled phase 3 studies documented significant reductions in visceral adipose tissue while preserving subcutaneous fat, alongside an increase in IGF-1. These findings apply to the respective subcutaneous mono-application, not to the combination.

You receive this blend as a research compound in 10 vials of 20 mg per vial (10 mg Retatrutide plus 10 mg Tesamorelin), as a lyophilizate for reconstitution. The format is intended for experimental research approaches.

This information is for research and educational purposes only. Not medical advice.

Studies

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What you need with it

Bacteriostatic water is added to your cart automatically. Syringes and swabs with one click.

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Bacteriostatic water

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Insulin Syringes

10 pcs · 5.50 €

Alcohol Swabs

50 pcs · 10 €

How much water?

Units on the syringe for your vial size.

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FAQ

Frequently asked

Sources for every answer: lexicon entry

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Is the Reta + Tesamorelin Blend approved or studied?

No. As of 26 October 2026 the registry ClinicalTrials.gov lists no trial with Retatrutide and tesamorelin together. Tesamorelin alone has been approved in the USA since 2010, Retatrutide is in phase 3 and not approved.

What is the catch with the fixed mix?

The two substances were studied on very different schedules: Retatrutide once a week, tesamorelin daily. In a 1:1 vial the ranges from both trial programmes cannot be matched at the same time. The entry therefore goes by the Retatrutide share.

What do the Retatrutide trials show?

In phase 2 body weight fell by 24.2 percent after 48 weeks at the highest study dose, by 2.1 percent on placebo. In phase 3 (TRIUMPH-1) it was 25.0 versus 3.9 percent after 80 weeks. A meta-analysis with 878 participants confirmed clear effects on weight and metabolic values.

What do the tesamorelin trials show?

In 806 patients with HIV and excess belly fat, visceral fat fell by 15.4 percent more than on placebo in 26 weeks, subcutaneous fat stayed nearly the same. IGF-1 rose, blood sugar stayed stable. Those who continued kept the effect to week 52.

Which side effects were seen with the components?

Retatrutide: mainly nausea, diarrhoea and other gastrointestinal effects, depending on the dose, plus a slight rise in heart rate. Tesamorelin: injection site reactions, joint and muscle pain, fluid retention and tingling. There is no safety profile for the blend.

Which trials are still running?

Nine phase 3 trials of Retatrutide are running, the largest on heart and kidney events until 2029. The phase 3 trials of tesamorelin were completed years ago. No trial of the blend is listed in the registry.

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