Reported results
Retatrutide: reported results by outcome
StatusPhase 3 · not FDA approved
PeptideHound Staff · Last editorially reviewed · 11 sources
The word results is doing two very different jobs in the searches that lead to this page. One means what a trial measured in people it enrolled, randomised and followed. The other means what somebody wrote in a thread. We report the first and do not collect the second, and this page concerns the distance between them.
What the trials measured is narrower than most summaries suggest. In the phase 2 obesity trial the primary end point was the percentage change in body weight from baseline to 24 weeks. In the phase 3 diabetes trial the primary endpoint was the change in HbA1c concentration from baseline to week 40, HbA1c being a blood-sugar average over about three months. A substudy of 98 participants measured liver fat instead.
The human record behind all of that runs to a few thousand people, over 48 weeks at the longest. It is unusually strong for a compound sold without approval, and it is still short. In the phase 3 trial, 490 of the 537 participants were still on study drug at the end and 504 of them, 94%, completed the study. That is a completion rate worth knowing before reading any average.
Because nothing has been approved, there is no post-marketing record of any kind: no label, no pharmacovigilance reporting, no registry of what happens to people outside a trial. What the FDA database holds instead is a single Class II recall of a compounded retatrutide injection, filed under lack of assurance of sterility.
Evidence: Outcomes from registered trials only · 1 published phase 3 trial, 537 randomised over 40 weeks · 1 phase 2 obesity trial, 338 adults over 48 weeks · 1 liver substudy in 98 participants · no reported experience is collected, aggregated or published on this page
Are retatrutide reviews and posted results evidence?
systematic review
No, and the cleanest way to see why is the placebo column in the published trials. We do not collect, aggregate or republish anybody's reported experience, and no figure published on this page originates in one. A 2025 systematic review of 26 randomised trials recorded how often adverse events appeared in participants who received a dummy injection, and the range it reports is GLP-1 RA vs. placebo: 80% to 97% vs. 63% to 100%.5 Read the second half of that range carefully: in some trials essentially every participant assigned to placebo reported something. That comparison is what a control group exists to supply, and it is precisely what a posted account cannot contain. A report without one is not a weaker version of a trial result but a different category of statement: an accurate record of what one person noticed, with nothing available to measure it against.
What outcomes have the retatrutide trials actually measured?
human RCT
Four, and knowing which four explains why so many reasonable questions remain unanswered. The phase 2 obesity trial measured body weight, with secondary end points that included the percentage change in body weight from baseline to 48 weeks and a weight reduction of 5% or more, 10% or more, or 15% or more.1 The phase 3 diabetes trial measured blood sugar instead, and records that the primary endpoint was the change in HbA1c concentration from baseline to week 40.8 Body weight was a secondary consideration there rather than the question the trial was designed around. The third outcome is liver fat, where a substudy set out to assess mean relative change from baseline in liver fat (LF) at 24 weeks in participants who already carried at least a tenth of their liver as fat.4 The fourth group of outcomes belongs to late-stage trials that have published nothing. Everything else people ask about — energy, sleep, mood, appetite as somebody would describe it — was never an endpoint anywhere.
What did the retatrutide phase 3 results show?
human RCT
One phase 3 trial has published, and it investigated blood sugar in type 2 diabetes rather than body weight. It ran 40 weeks and randomised 537 adults whose diabetes was inadequately controlled by diet and exercise alone.8 The headline numbers are blood-sugar numbers. The mean change from baseline in HbA1c concentration was -1·69% (SE 0·11) with retatrutide 4 mg, -1·86% (0·10) with 9 mg, and -1·94% (0·08) with 12 mg, versus -0·81% (0·12) with placebo.8 The placebo line is the one to hold on to, because that column moved as well. Roughly four fifths of a percentage point came off in participants receiving no active compound whatsoever, which is a measure of what dietary change, clinical attention and participation in a trial accomplish by themselves. The trial's own conclusion is cautious in the same way, describing an adverse event profile consistent with molecules with GLP-1 agonist activity.8
Who were these results measured in?
systematic review
This question determines how much a published average has to do with any particular reader, and it is almost never printed alongside the averages themselves. The phase 2 diabetes trial enrolled a group with a mean age 56·2 years [SD 9·7], mean duration of diabetes 8·1 years [7·0], 156 [56%] female, and 235 [84%] White.2 The phase 3 trial recruited a younger and earlier group, where baseline mean age was 48·8 years (SD 12·1), mean HbA1c concentration was 7·9% (SD 1·1), mean duration of diabetes was 2·5 years (SD 4·4), and mean BMI was 35·8 kg/m2 (SD 7·0).8 Across the wider literature the picture is similar. A 2025 systematic review of this class describes participants with a mean body mass index, 30 to 41 kg/m2; mean age, 34 to 57 years.5 A result measured in a particular population remains a result about that population rather than a general characteristic of the compound.
How many people actually finished the trials?
human RCT
More than most people assume, and both trials that reported it published the arithmetic. In the phase 3 diabetes trial, 490 of the 537 randomised participants were still receiving study drug at the end and 504 of them, 94%, completed the study itself.8 The earlier phase 2 diabetes trial ran lower on both counts. There, 237 (84%) participants completed the study and 222 (79%) completed study treatment, which means roughly a fifth of the people who started did not finish on the compound they had been assigned.2 That discrepancy belongs beside every average on this page, because an average reported at a trial's conclusion describes only the participants still present to be measured. Those who discontinued are less a footnote to the result than an unreported component of it.
What did the liver substudy measure?
human RCT
It measured fat inside the liver, in a group picked for having a lot of it. Everyone came from the obesity trial, had fatty liver disease, and started with at least a tenth of the organ made up of fat.4 The measure is a scan rather than a symptom. Nobody in the substudy was asked how they felt, so no result from it describes anything a person would notice day to day. What the investigators report is a link rather than a lone number. In those participants, LF reductions were significantly related to changes in body weight, abdominal fat and metabolic measures associated with improved insulin sensitivity and lipid metabolism.4 So liver fat moved with body weight rather than apart from it, which is a narrower finding than a headline percentage suggests, and it is still the only organ-level outcome published for this compound.
What is being measured in the trials that have not reported?
human pilot / early trial
Three outcomes no study among the research behind this page has published yet, and two of them have nothing to do with weight. In the late-stage programme the weight trials measure percent change in body weight, while a sleep apnea protocol measures change in Apnea-Hypopnea Index and a knee protocol scores joint pain.7 Apnea-Hypopnea Index counts breathing interruptions per hour of sleep. The knee score is a questionnaire filled in by the patient. Both are real measures, and neither has produced a published number for this compound. The registry lists more of the same. A Study of Retatrutide (LY3437943) in Participants With Obesity and Cardiovascular Disease is marked COMPLETED with no published result, and a phase 1 study of Insulin Secretion and Insulin Sensitivity is still listed as ACTIVE_NOT_RECRUITING.910 Completed and published are different things, and that gap is where most of this evidence sits today.
How much of the result is fat, and how much is not?
review
No study among the research behind this page has published the split for retatrutide, and the class-level estimate is large enough that the omission matters. A 2024 review of this family reports that these agents cause a loss of lean mass of about 10% or about 6 kg, comparable to a decade or more of aging in the adults studied.3 Read what that figure is. It is a review's summary across incretin compounds rather than a measurement inside a retatrutide trial, and no published retatrutide trial has reported body composition at all. The number is the best available and it is not about this compound specifically. The same review points at what might change it, noting that supervised resistance exercise training interventions with a duration >10 weeks can elicit large increases in lean mass (∼3 kg) and strength (∼25%) in men and women.3 That has not been tested alongside retatrutide either.
What results do women see?
systematic review
Women made up most of the people measured, and not one published analysis reports their results separately. Those two facts sit oddly together and they are both true. The proportions are on the record. A 2025 systematic review of this class describes a pooled population that was 72% female.5 The phase 3 retatrutide trial randomised 537 (296 [55%] female and 241 [45%] male) participants, and the phase 2 diabetes trial counted 156 [56%] female among its 281.82 So the published averages are already weighted towards women, which is not the same thing as an answer about women. A result reported separately by sex would tell a reader whether the effect differs, and no such breakdown has been published for retatrutide in any trial.
Why do posted results and trial results disagree?
human RCT
Four reasons, none of which requires anybody to be dishonest. The first is the absence of a control group, which a posted account cannot possibly supply, leaving nothing for the reported change to be measured against. The second is who is being described. Trials recruit against written criteria, and the phase 2 diabetes trial took adults aged 18-75 years with type 2 diabetes who also met thresholds for blood sugar and body size.2 A reader outside those boundaries was never studied, and no published figure describes them. The third is the material itself. A trial participant received a known compound at a known strength, while the FDA database holds a Class II recall of a compounded retatrutide injection filed under lack of assurance of sterility.11 The fourth is selection. A result dramatic enough to be worth posting is by definition unrepresentative, and nobody composes an account of an uneventful eleven months.
How strong is the evidence behind these results?
systematic review
Strong for a compound nobody has approved, and still short in the ways that matter most. The trials are randomised and placebo-controlled, which puts them well above most of what this site covers. The limits are printed by the reviewers themselves. A 2025 systematic review of 26 randomised trials reports that no head-to-head RCTs were available and that heterogeneity prevented meta-analysis, so the figures were never pooled into one estimate.5 A 2025 review of the wider pipeline identified 53 phase 3 and phase 2 trials across the field and records that completed phase 2 trials on incretin-based therapies showed a mean percent weight loss of 7.4% to 24.2%.6 That last range is the honest version of every headline number. It spans most of the useful territory, it comes from different compounds in different people, and the top of it is not a prediction for anyone.
Is retatrutide worth it?
systematic review
That is a judgement about a reader's own circumstances, and it is not ours to make. What we can do is set the measured outcomes against the unmeasured ones, which is the material anybody would need to decide it themselves. Measured: body weight over 48 weeks, blood sugar over 40 weeks and liver fat over 24 weeks, all in randomised trials carrying placebo groups. Unmeasured: everything after stopping, everything beyond a year, the fat and muscle split, and anything concerning material obtained outside a trial. A 2025 systematic review names the same hole from the research end, stating that data on mortality and obesity-related complications, such as cardio-renal-metabolic events, are needed.6 That is the sentence a reader should weigh hardest, because it says the outcomes people actually care about have not been measured yet, rather than that they have been measured and look fine.
What we don’t know
The gaps in the evidence matter as much as the findings.
- 01What happens after a course ends. No trial among the research behind this page has followed anybody off retatrutide, and the longest published course runs 48 weeks.
- 02How results break down by sex. Women were the majority in these trials, and no analysis among the research behind this page reports the outcomes separately for them.
- 03What the results look like week by week. The trials measured at scheduled visits, so a one-week or one-month figure has no published counterpart at all.
- 04Whether anything measured in a trial transfers to material bought elsewhere. No analysis among the research behind this page reports the purity, identity or sterility of anything sold under this name.
- 05What the late-stage studies will show. Four phase 3 trials in over 5800 participants are running, and no study we cite has yet reported an outcome for sleep apnea or knee pain.
- 06Whether the weight change is mostly fat. The class-level estimate for lean-mass loss comes from a review rather than from a retatrutide trial that measured body composition.
- 07What happens over years. Every published result stops inside twelve months, and mortality and complication data are still listed as needed.
Sources
- 1Triple-Hormone-Receptor Agonist Retatrutide for Obesity - A Phase 2 Trial N Engl J Med 2023. doi:10.1056/NEJMoa2301972human RCT
- 2Retatrutide, a GIP, GLP-1 and glucagon receptor agonist, for people with type 2 diabetes: a randomised, double-blind, placebo and active-controlled, parallel-group, phase 2 trial conducted in the USA Lancet 2023. doi:10.1016/S0140-6736(23)01053-Xhuman RCT
- 3Incretin-Based Weight Loss Pharmacotherapy: Can Resistance Exercise Optimize Changes in Body Composition? Diabetes Care 2024. doi:10.2337/dci23-0100review
- 4Triple hormone receptor agonist retatrutide for metabolic dysfunction-associated steatotic liver disease: a randomized phase 2a trial Nat Med 2024. doi:10.1038/s41591-024-03018-2human RCT
- 5Efficacy and Safety of Glucagon-Like Peptide-1 Receptor Agonists for Weight Loss Among Adults Without Diabetes: A Systematic Review of Randomized Controlled Trials Ann Intern Med 2025. doi:10.7326/ANNALS-24-01590systematic review
- 6Emerging pharmacotherapies for obesity: A systematic review Pharmacol Rev 2025. doi:10.1124/pharmrev.123.001045systematic review
- 7Retatrutide for obesity, obstructive sleep apnea and knee osteoarthritis: Rationale and design of the TRIUMPH registrational clinical trials Diabetes Obes Metab 2026. doi:10.1111/dom.70209human pilot / early trial
- 8Efficacy and safety of retatrutide, a GIP, GLP-1, and glucagon receptor agonist, in people with type 2 diabetes and inadequate glycaemic control with diet and exercise (TRANSCEND-T2D-1) Lancet 2026. doi:10.1016/S0140-6736(26)00967-0human RCT
- 9A Study of Retatrutide (LY3437943) in Participants With Obesity and Cardiovascular Disease NCT05882045registered trial
- 10A Study to Evaluate the Effect of Retatrutide on Insulin Secretion and Insulin Sensitivity in Adult Participants With Type 2 Diabetes Mellitus NCT06982859registered trial
- 11Retatrutide for Injection, 60mg / 10mL vial, all presentations, recalled for lack of assurance of sterility 2025. sourceregulatory action
