Zepbound weight loss chart: SURMOUNT trial results

In SURMOUNT-1, the main 72-week trial in 2,539 adults without diabetes, average weight changed −15.0%, −19.5% and −20.9% with Zepbound 5, 10 and 15 mg, against −3.1% with placebo, as reported in the FDA label. Adults with type 2 diabetes lost less (−12.8% and −14.7% at 10 and 15 mg in SURMOUNT-2). These are trial averages and do not predict any one person’s result.

Checked against the FDA label and cited trials on

Peptide Library is an independent educational resource. It is not affiliated with, sponsored or endorsed by Novo Nordisk or Eli Lilly; Ozempic, Wegovy, Mounjaro and Zepbound are trademarks of their owners and are named only to identify the products. This page summarizes FDA-approved prescribing information and published trials. It is not individual medical advice: dosing and any change to it are decided with a prescriber.

The product

Zepbound (tirzepatide)

Manufacturer
Eli Lilly
Form
Once-weekly injection: single-dose pens or vials (2.5 to 15 mg), multi-dose KwikPen or vial
FDA-approved uses
  • Reducing excess body weight and keeping it off long term in adults with obesity, or overweight with a weight-related condition
  • Moderate to severe obstructive sleep apnea in adults with obesity
Boxed warning
Risk of thyroid C-cell tumors: tirzepatide caused thyroid C-cell tumors in rats; whether it does in humans is unknown. Contraindicated with a personal or family history of medullary thyroid carcinoma or MEN 2.

Prescribing information · Tirzepatide research profile

Trial results, one trial at a time

Group averages from selected trial populations, each beside its own trial’s comparator. They do not predict any one person’s result, and figures from different trials are not compared with each other.

SURMOUNT-1

NCT04184622 on ClinicalTrials.gov

Phase
Phase 3
Status
Completed
Population
Adults with obesity, or overweight with a weight-related condition, without type 2 diabetes
Randomized
2,539
Duration
72 weeks
Comparator
Placebo

Reported results

SURMOUNT-1: Mean % change in body weight, Week 72Label section 14: all randomized patients, missing data imputed from retrieved dropouts
Zepbound 5 mg−15.0%Zepbound 10 mg−19.5%Zepbound 15 mg−20.9%Placebo−3.1%
SURMOUNT-1: Mean % change in body weight at Week 72, by arm
ArmReportedAnalysed
Zepbound 5 mg−15.0%n=630
Zepbound 10 mg−19.5%n=636
Zepbound 15 mg−20.9%n=630
Placebo(comparator)−3.1%n=643

FDA prescribing information: Zepbound (tirzepatide) prescribing information, DailyMed, effective 2026-08-28

SURMOUNT-2

NCT04657003 on ClinicalTrials.gov

Phase
Phase 3
Status
Completed
Population
Adults with BMI ≥27 and type 2 diabetes
Randomized
938
Duration
72 weeks
Comparator
Placebo

Reported results

SURMOUNT-2: Mean % change in body weight, Week 72Label section 14: all randomized patients, missing data imputed from retrieved dropouts
Zepbound 10 mg−12.8%Zepbound 15 mg−14.7%Placebo−3.2%
SURMOUNT-2: Mean % change in body weight at Week 72, by arm
ArmReportedAnalysed
Zepbound 10 mg−12.8%n=312
Zepbound 15 mg−14.7%n=311
Placebo(comparator)−3.2%n=315

FDA prescribing information: Zepbound (tirzepatide) prescribing information, DailyMed, effective 2026-08-28

  • People with type 2 diabetes lost less weight than people without it in both tirzepatide and semaglutide programs; compare SURMOUNT-1 and SURMOUNT-2 only as separate trials.

SURMOUNT-3

NCT04657016 on ClinicalTrials.gov

Phase
Phase 3
Status
Completed
Population
Adults who first lost at least 5% in a 12-week intensive lifestyle program
Randomized
579
Duration
72 weeks after randomization
Comparator
Placebo

Reported results

SURMOUNT-3: Mean % change in body weight, Week 72 (from randomization)Label section 14: all randomized patients, missing data imputed from retrieved dropouts
Zepbound (maximum tolerat…−18.4%Placebo+2.5%
SURMOUNT-3: Mean % change in body weight at Week 72 (from randomization), by arm
ArmReportedAnalysed
Zepbound (maximum tolerated 10 or 15 mg)−18.4%n=287
Placebo(comparator)+2.5%n=292

FDA prescribing information: Zepbound (tirzepatide) prescribing information, DailyMed, effective 2026-08-28

  • Measured from randomization, after the lifestyle lead-in: the figures are not comparable with SURMOUNT-1.

SURMOUNT-4 (stopping vs continuing)

NCT04660643 on ClinicalTrials.gov

Phase
Phase 3
Status
Completed
Population
Adults who lost weight on 36 weeks of open-label Zepbound, then were randomized to continue or switch to placebo
Randomized
670
Duration
Week 36 to week 88
Comparator
Placebo (treatment withdrawn)

Reported results

SURMOUNT-4 (stopping vs continuing): Mean % change in body weight from week 36, Week 88Label section 14: all randomized patients, missing data imputed from retrieved dropouts
Continued Zepbound−5.5%Switched to placebo+14.0%
SURMOUNT-4 (stopping vs continuing): Mean % change in body weight from week 36 at Week 88, by arm
ArmReportedAnalysed
Continued Zepbound−5.5%n=335
Switched to placebo(comparator)+14.0%n=335

FDA prescribing information: Zepbound (tirzepatide) prescribing information, DailyMed, effective 2026-08-28

  • The lead-in averaged −20.9%. Weight came back for most people who stopped, which is why the label speaks of maintaining weight reduction long term.

SURMOUNT-OSA (two trials)

NCT05412004 on ClinicalTrials.gov

Phase
Phase 3
Status
Completed
Population
Adults with obesity and moderate to severe obstructive sleep apnea, without (trial 1) or with (trial 2) PAP therapy
Randomized
469
Duration
52 weeks
Comparator
Placebo

Reported results

SURMOUNT-OSA (two trials): AHI change, trial 1 (no PAP), Week 52Label section 14, modified intention-to-treat
Zepbound−25.3 events per hourPlacebo−5.3 events per hour
SURMOUNT-OSA (two trials): AHI change, trial 1 (no PAP) at Week 52, by arm
ArmReported
Zepbound−25.3 events per hour
Placebo(comparator)−5.3 events per hour

FDA prescribing information: Zepbound (tirzepatide) prescribing information, DailyMed, effective 2026-08-28

  • Body weight changed −17.7% and −19.6% with Zepbound vs −1.6% and −2.3% with placebo in the two trials.

How to read the chart

Each panel is one trial, with every dose beside that trial’s placebo group. The trials enrolled different people for different lengths of time, so a figure from one trial is not compared with a figure from another. SURMOUNT-3 and SURMOUNT-4 measure from a later starting point (after a lifestyle program, or after 36 weeks of treatment), and SURMOUNT-4 shows what happened when treatment was stopped.

Figures are the label’s least-squares means for all randomized participants, with missing data imputed from people who stopped treatment (retrieved dropouts). The label’s section 14 is the source for every number unless the panel says otherwise.

Side effects in the label

In the pooled SURMOUNT-1 and SURMOUNT-2 data, nausea was reported in 25%, 29% and 28% on 5, 10 and 15 mg vs 8% on placebo; diarrhea 19%, 21% and 23% vs 8%; vomiting 8%, 11% and 13% vs 2%; constipation 17%, 14% and 11% vs 5%. Stopping because of adverse reactions: 4.8%, 6.3% and 6.7% vs 3.4%.

Zepbound compared with semaglutide

The one randomized head-to-head trial, SURMOUNT-5 (NEJM 2025, open-label, 751 adults with obesity, 72 weeks), reported −20.2% with tirzepatide at the maximum tolerated dose (10 or 15 mg) vs −13.7% with semaglutide at the maximum tolerated dose (1.7 or 2.4 mg). It was funded by Eli Lilly and is not part of either label.

Questions

How much weight do people lose on Zepbound?

In SURMOUNT-1 the average change at 72 weeks was −15.0% (5 mg), −19.5% (10 mg) and −20.9% (15 mg) vs −3.1% with placebo, per the FDA label. Individual results vary widely and the averages do not predict any one person’s.

What happens if you stop Zepbound?

In SURMOUNT-4, people switched to placebo after 36 weeks changed by an average of +14.0% from their week-36 weight by week 88, while those who continued changed by −5.5%.

Is Zepbound the same as Mounjaro?

Both contain tirzepatide, but they are separate FDA-approved products with different indications: Zepbound for weight management and sleep apnea, Mounjaro for type 2 diabetes. See Mounjaro vs Zepbound.

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