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Retatrutide Results Timeline

Retatrutide Results Timeline: What the Trials Measured

The short answer

This page is general educational information, research-use framing only, not medical advice. Any decision about a research compound belongs with a qualified clinician.

TL;DR

The retatrutide results timeline comes from one 48 week phase 2 trial, not from personal reports. In the highest dose group (12 mg), mean body weight fell about 17.5% by week 24 and about 24.2% by week 48 (Jastreboff et al., 2023). These are group averages measured under research conditions, not a forecast for any one person, and any decision about retatrutide belongs to a qualified clinician.

- Retatrutide, a triple receptor agonist (GIP, GLP-1, and glucagon), was tested in a 48 week phase 2 trial that tracked mean body-weight change over time (Jastreboff et al., 2023). - In the highest dose group (12 mg), mean body weight fell about 17.5% by week 24 and about 24.2% by week 48 (Jastreboff et al., 2023). These are group averages, not a promise to any one person. - Weight loss on incretin-class therapy is steepest early and tends to slow toward a plateau over time (Wilding et al., 2021, STEP 1), partly because energy expenditure drops as weight comes off (Rosenbaum and Leibel, 2010). - Retatrutide's 48 week mean is numerically higher than tirzepatide in SURMOUNT-1 (up to about 22.5%, 72 weeks) and semaglutide in STEP 1 (about 15%, 68 weeks), but the trials differ in length and design (Jastreboff et al., 2022; Wilding et al., 2021). - When incretin therapy stops, trials of related compounds report meaningful weight regain (Aronne et al., 2024; Wilding et al., 2022). Any personal decision or dose belongs to a qualified clinician.

What did the retatrutide trial measure over time?

The phase 2 trial tracked mean percentage change in body weight across 48 weeks in adults with obesity, with the largest reductions in the highest dose group (Jastreboff et al., 2023).

This was a randomized, placebo-controlled trial that assigned participants to several dose groups, up to 12 mg. The main readout was percentage change in body weight, measured at set checkpoints through week 48. The page below reports those phase 2 results only; results from larger, later trials are not published here.

One point matters for a timeline: these numbers are group means. The trial reported the average change across everyone in a dose group. Individual participants sat above and below that average.

How much weight loss did retatrutide show at 24 weeks?

In the 12 mg group, mean body weight fell about 17.5% by week 24 (Jastreboff et al., 2023).

Week 24 is the halfway mark of the 48 week trial. Reaching about 17.5% by the midpoint tells you the early part of the curve is where most of the change accumulated. That early-and-fast pattern is common across incretin-class research and is one reason a results timeline looks like a steep slope that gradually bends.

How much at 48 weeks, the full trial window?

By week 48, the 12 mg group reached a mean of about 24.2% below baseline (Jastreboff et al., 2023).

This is the top-line figure most often quoted for retatrutide. All reductions in the active dose groups were larger than the placebo group over the same window.

The ranges below reflect what published studies and commonly studied research protocols report. This is educational, not a prescription or a personal recommendation. The "12 mg" label is the trial dose group, reported so the timeline numbers have context, not a dose for the reader.

Trial timepointReported mean body-weight change, 12 mg groupSource
Baseline0% (reference)Jastreboff et al., 2023
Week 24about -17.5%Jastreboff et al., 2023
Week 48 (trial end)about -24.2%Jastreboff et al., 2023

A detail worth flagging: in the phase 2 trial, mean weight was still trending down at week 48 in the higher dose groups (Jastreboff et al., 2023). That means the 48 week figure may not represent a final plateau, and it should not be read as a ceiling or a target.

Why does the results curve slow down over time?

Weight loss on incretin-class therapy is fastest early and tends to flatten as the body adapts (Wilding et al., 2021, STEP 1; Rosenbaum and Leibel, 2010).

Two things drive the bend in the curve. First, in the STEP 1 semaglutide trial, weight fell from the first check at week 4, reached its lowest point (nadir) near week 60, and the rate of loss slowed well before that, so the curve flattens with time on treatment (Wilding et al., 2021). Second, as a person loses weight, resting energy expenditure falls more than body-size change alone would predict, a response called adaptive thermogenesis (Rosenbaum and Leibel, 2010). This physiology resists further loss and helps explain why early weeks show the biggest moves.

How does the retatrutide timeline compare to tirzepatide and semaglutide?

Retatrutide's 48 week mean is numerically the highest of the three, but each trial ran for a different length, so the timelines are not a fair head-to-head (Jastreboff et al., 2023; Jastreboff et al., 2022; Wilding et al., 2021).

Compound (dose)TrialTrial lengthReported top-line meanSource
Retatrutide (12 mg)Phase 248 weeksup to about -24.2%Jastreboff et al., 2023
TirzepatideSURMOUNT-172 weeksup to about -22.5%Jastreboff et al., 2022
SemaglutideSTEP 168 weeksabout -15%Wilding et al., 2021

Read the table with care. Retatrutide reached about 24.2% in 48 weeks, while the tirzepatide and semaglutide figures come from longer trials of 72 and 68 weeks. Different enrollment, dose schedules, and endpoints also separate these studies. The honest read is that retatrutide's phase 2 numbers look strong on their own timeline, not that one drug "beats" another in a direct comparison.

What happens to results after the trial or after stopping?

Trials of related incretin therapies report meaningful weight regain after treatment stops (Aronne et al., 2024; Wilding et al., 2022).

When tirzepatide was withdrawn in SURMOUNT-4, participants regained a substantial share of lost weight (Aronne et al., 2024). A similar pattern appeared after semaglutide stopped in the STEP 1 extension (Wilding et al., 2022). The adaptive thermogenesis physiology above is part of why (Rosenbaum and Leibel, 2010). Retatrutide-specific withdrawal data is limited in the published record here, so this pattern is inferred from related GLP-1-class trials rather than measured on retatrutide directly.

Should I expect this timeline for myself?

No. These are averages from a controlled research setting, not a forecast for any individual, and any decision about retatrutide belongs to a qualified clinician.

Group means hide wide individual variation. Trial participants were screened, monitored, and supported in ways that do not match self-guided use. This page is research education. It does not recommend retatrutide, a dose, or a schedule, and it makes no promise about what any reader will see in any number of weeks. In the trial, the highest dose group received 12 mg (Jastreboff et al., 2023); whether any compound or dose is appropriate for a given person is a clinical question, not a self-service one.

FAQ schema

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Retatrutide Results Timeline: FAQ

References

  1. Jastreboff AM, Kaplan LM, Frias JP, et al. Triple-Hormone-Receptor Agonist Retatrutide for Obesity: A Phase 2 Trial. N Engl J Med. 2023;389(6):514-526. doi:10.1056/NEJMoa2301972. PMID 37366315.
  2. Jastreboff AM, Aronne LJ, Ahmad NN, et al. Tirzepatide Once Weekly for the Treatment of Obesity (SURMOUNT-1). N Engl J Med. 2022;387(3):205-216. doi:10.1056/NEJMoa2206038. PMID 35658024.
  3. Wilding JPH, Batterham RL, Calanna S, et al. Once-Weekly Semaglutide in Adults with Overweight or Obesity (STEP 1). N Engl J Med. 2021;384(11):989-1002. doi:10.1056/NEJMoa2032183. PMID 33567185.
  4. Aronne LJ, Sattar N, Horn DB, et al. Continued Treatment With Tirzepatide for Maintenance of Weight Reduction in Adults With Obesity: The SURMOUNT-4 Randomized Clinical Trial. JAMA. 2024;331(1):38-48. doi:10.1001/jama.2023.24945.
  5. Wilding JPH, Batterham RL, Davies M, et al. Weight regain and cardiometabolic effects after withdrawal of semaglutide: The STEP 1 trial extension. Diabetes Obes Metab. 2022;24(8):1553-1564. doi:10.1111/dom.14725. PMC9542252.
  6. Rosenbaum M, Leibel RL. Adaptive thermogenesis in humans. Int J Obes (Lond). 2010;34(Suppl 1):S47-S55. doi:10.1038/ijo.2010.184.

General educational information only, research-use framing, not medical advice. Confirm the current status where you live and consult a qualified professional before acting.

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