PX1 / 10 mg
Retatrutide
An investigational molecule studied across three metabolic signaling pathways.
For research use only. Not intended for human use.
The research information on this page describes published studies about the molecule and does not demonstrate the effect, safety, purity, or quality of PX1Labs' research material.

01
What is it?
10 mgRetatrutide is an investigational peptide and triple agonist acting at GIP, GLP-1 and glucagon receptors.
60 sec
In simple terms
Retatrutide is still being studied. Scientists are testing how it sends three different signals linked with hunger, blood sugar and how the body uses energy. It is not an approved medicine, and a study result cannot prove what is in a particular vial or how that vial affects a person.
Retatrutide / explained
Retatrutide, clearly explained
The repeated themes across the 30 submitted graphics are consolidated into 15 checked cards. Swipe from the basics through trial results and safety.
These cards describe published research and current regulatory status. They are not instructions for use or proof of a particular vial's contents, quality or effect.
02
What is being studied?
- 01
Body-weight change in clinical trials
- 02
Glucose and metabolic measures
- 03
Safety and adverse events over longer follow-up
Retatrutide / scientific overview
A metabolic signal studied across three receptors
Retatrutide (LY3437943) is an investigational triple agonist that activates GIP, GLP-1 and glucagon receptors. This combination is studied in the context of appetite and satiety signaling, glucose metabolism, energy expenditure and fat oxidation. These mechanisms describe the investigational molecule, not a proven effect of a PX1Labs vial.
How the three signaling pathways are studied
Role in research · Important context
- Signal
- GLP-1
- Role in research
- Associated with satiety signaling, slower gastric emptying and glucose-dependent insulin response.
- Important context
- Clinical trials assess it together with the other receptor pathways, not in isolation.
- Signal
- GIP
- Role in research
- Participates in post-meal insulin response and glucose and lipid metabolic signaling.
- Important context
- Retatrutide research examines the potential interaction between GIP and GLP-1.
- Signal
- Glucagon
- Role in research
- Studied in relation to energy expenditure, lipolysis and fatty-acid oxidation.
- Important context
- Mechanistic evidence for fat oxidation is partly preclinical; its independent contribution in humans is not fully established.
Research highlights
- mean body-weight change in the 12 mg group at 48 weeks in the Phase 2 obesity trial
- −24.2%
- largest mean HbA1c change at 36 weeks in the Phase 2 type 2 diabetes trial
- −2.16 pp
- relative liver-fat change in the 12 mg group at 24 weeks in the MASLD substudy
- −82.4%
Clinical evidence
Phase · Duration · Published result
- Population
- Obesity or overweight without diabetes
- Phase
- Phase 2
- Duration
- 48 weeks
- Published result
- Mean body-weight change was −22.8% in the 8 mg group and −24.2% in the 12 mg group.
- Population
- Type 2 diabetes
- Phase
- Phase 2
- Duration
- 36 weeks
- Published result
- HbA1c decreased by up to 2.16 percentage points in the highest groups; body-weight change reached approximately −17%.
- Population
- MASLD substudy
- Phase
- Phase 2 substudy
- Duration
- 24 weeks
- Published result
- Relative liver-fat change was −81.4% in the 8 mg group and −82.4% in the 12 mg group.
Cross-trial comparison
Receptors · Research context · Mean body-weight change
- Molecule
- Semaglutide
- Receptors
- GLP-1
- Research context
- STEP 1, obesity or overweight
- Mean body-weight change
- −14.9% / 68 weeks
- Molecule
- Tirzepatide
- Receptors
- GIP + GLP-1
- Research context
- SURMOUNT-1, obesity or overweight
- Mean body-weight change
- up to −20.9% / 72 weeks
- Molecule
- Retatrutide
- Receptors
- GIP + GLP-1 + glucagon
- Research context
- Phase 2, obesity or overweight
- Mean body-weight change
- up to −24.2% / 48 weeks
These values come from separate trials with different protocols, durations and analysis methods. They are not a head-to-head comparison and do not establish that one molecule is superior to another.
Clinical and regulatory status
In 2026, Eli Lilly reported initial topline results from several Phase 3 trials, but retatrutide remains investigational. The FDA states that it is not a component of an FDA-approved drug and has not been found safe and effective for any condition. Sponsor press releases do not replace peer-reviewed full publications or regulatory approval.
03
What to keep in mind
Retatrutide is not an approved medicine. Results from molecule research do not establish the effect, purity or quality of PX1Labs material.
Videos and conversations
Community / evidence
Positive experiences shared by people
A selection of public posts in which people describe their own positive experience with retatrutide.
These positive public stories were selected deliberately. They are not PX1Labs customer reviews, have not been independently verified and do not show a typical or guaranteed result.
Read the sources