Skip to content

Study · Randomized controlled trial · n = 2,539 · 2022

6 results

Tirzepatide Once Weekly for the Treatment of Obesity.

Jastreboff AM, Aronne LJ, Ahmad NN, Wharton S, Connery L, Alves B, Kiyosue A, Zhang S, Liu B, Bunck MC, Stefanski A

The New England journal of medicine4 Jun 2022Cited by 2,802 (Europe PMC)

Summary

The text of this summary is not shown here, because the article license does not allow reuse. Read it at the source (opens in a new tab)

Text rights: Publisher copyright. Results still quote short attributed sentences.

Results from this study6

6 results from studies that gave the peptide. 6 results from people.

  1. 01HumanRandomized controlled trialEfficacy outcome

    In adults with obesity without diabetes, tirzepatide 5, 10 and 15 mg once weekly reduced body weight at week 72 by 15.0%, 19.5% and 20.9%, versus 3.1% with placebo, a significant difference for every dose.

    In plain wordsIn adults with obesity, weight loss after 72 weeks was greater with tirzepatide than with placebo.

    Outcome
    DecreasePercentage change in body weight at week 72
    Study

    n = 2,539

    Comparator
    Placebo
    Analysis
    Primary
    Outcome group
    Body weight · Metabolic and weight
    Studied dose
    5 mg, 10 mg or 15 mg once weekly · subcutaneous · 72 weeks, including a 20-week dose-escalation periodAs given in this study (human).

    Measurements

    Mean percentage weight reduction at week 72
    15%
    tirzepatide 5 mg
    Mean percentage weight reduction at week 72
    19.5%
    tirzepatide 10 mg
    Mean percentage weight reduction at week 72
    20.9%
    tirzepatide 15 mg
    Mean percentage weight reduction at week 72
    3.1%
    placebo

    Source sentences

    Summary
    The mean percentage change in weight at week 72 was -15.0% (95% confidence interval [CI], -15.9 to -14.2) with 5-mg weekly doses of tirzepatide, -19.5% (95% CI, -20.4 to -18.5) with 10-mg doses, and -20.9% (95% CI, -21.8 to -19.9) with 15-mg doses and -3.1% (95% CI, -4.3 to -1.9) with placebo (P<0.0…
    1 context sentence
    Summary · context
    we assigned 2539 adults with a body-mass index (BMI; the weight in kilograms divided by the square of the height in meters) of 30 or more, or 27 or more and at least one weight-related complication, excluding diabetes, in a 1:1:1:1 ratio to receive once-weekly, subcutaneous tirzepatide (5 mg, 10 mg,…
  2. 02HumanRandomized controlled trialEfficacy outcome

    In adults with obesity without diabetes, most participants on tirzepatide 5, 10 and 15 mg once weekly achieved a weight reduction of 5% or more, a much larger share than with placebo.

    In plain wordsIn adults with obesity, more people lost at least 5% of their body weight with tirzepatide than with placebo.

    Outcome
    IncreaseProportion with weight reduction of 5% or more
    Study

    n = 2,539

    Comparator
    Placebo
    Analysis
    Primary
    Outcome group
    Body weight · Metabolic and weight
    Studied dose
    5 mg, 10 mg or 15 mg once weekly · subcutaneous · 72 weeks, including a 20-week dose-escalation periodAs given in this study (human).

    Source sentences

    Summary
    The percentage of participants who had weight reduction of 5% or more was 85% (95% CI, 82 to 89), 89% (95% CI, 86 to 92), and 91% (95% CI, 88 to 94) with 5 mg, 10 mg, and 15 mg of tirzepatide, respectively, and 35% (95% CI, 30 to 39) with placebo
    1 context sentence
    Summary · context
    we assigned 2539 adults with a body-mass index (BMI; the weight in kilograms divided by the square of the height in meters) of 30 or more, or 27 or more and at least one weight-related complication, excluding diabetes, in a 1:1:1:1 ratio to receive once-weekly, subcutaneous tirzepatide (5 mg, 10 mg,…
  3. 03HumanRandomized controlled trialEfficacy outcome

    In adults with obesity without diabetes, a much larger share of participants on tirzepatide 10 mg and 15 mg than on placebo had a body weight reduction of 20% or more (about half or more, versus very few with placebo).

    In plain wordsIn adults with obesity, more people lost at least 20% of their body weight with tirzepatide 10 mg or 15 mg than with placebo.

    Outcome
    IncreaseProportion with weight reduction of 20% or more
    Study

    n = 2,539

    Comparator
    Placebo
    Outcome group
    Body weight · Metabolic and weight
    Studied dose
    10 mg or 15 mg once weekly · subcutaneous · 72 weeks, including a 20-week dose-escalation periodAs given in this study (human).

    Source sentences

    Summary
    50% (95% CI, 46 to 54) and 57% (95% CI, 53 to 61) of participants in the 10-mg and 15-mg groups had a reduction in body weight of 20% or more, as compared with 3% (95% CI, 1 to 5) in the placebo group
    1 context sentence
    Summary · context
    we assigned 2539 adults with a body-mass index (BMI; the weight in kilograms divided by the square of the height in meters) of 30 or more, or 27 or more and at least one weight-related complication, excluding diabetes, in a 1:1:1:1 ratio to receive once-weekly, subcutaneous tirzepatide (5 mg, 10 mg,…
  4. 04HumanRandomized controlled trialEfficacy outcome

    In adults with obesity without diabetes, the authors reported improvements in all prespecified cardiometabolic measures with tirzepatide.

    In plain wordsIn adults with obesity, the authors reported improvements in all the heart and metabolism measures they had planned to check with tirzepatide.

    Outcome
    Direction not reportedPrespecified cardiometabolic measures
    Study

    n = 2,539

    Outcome group
    Cardiometabolic risk factors · Metabolic and weight
    Studied dose
    5 mg, 10 mg or 15 mg once weekly · subcutaneous · 72 weeks, including a 20-week dose-escalation periodAs given in this study (human).

    Source sentences

    Summary
    Improvements in all prespecified cardiometabolic measures were observed with tirzepatide.
    1 context sentence
    Summary · context
    we assigned 2539 adults with a body-mass index (BMI; the weight in kilograms divided by the square of the height in meters) of 30 or more, or 27 or more and at least one weight-related complication, excluding diabetes, in a 1:1:1:1 ratio to receive once-weekly, subcutaneous tirzepatide (5 mg, 10 mg,…
  5. 05HumanRandomized controlled trialSafety outcome

    In adults with obesity without diabetes, the most common adverse events with tirzepatide were gastrointestinal, mostly mild to moderate and occurring mainly during dose escalation.

    In plain wordsIn adults with obesity, the most common side effects of tirzepatide were stomach and gut problems, mostly mild to moderate, mainly during dose increases.

    Outcome
    Not applicableGastrointestinal adverse events
    Study

    n = 2,539

    Outcome group
    Gastrointestinal adverse events · Gastrointestinal
    Studied dose
    5 mg, 10 mg or 15 mg once weekly · subcutaneous · 72 weeks, including a 20-week dose-escalation periodAs given in this study (human).

    Source sentences

    Summary
    The most common adverse events with tirzepatide were gastrointestinal, and most were mild to moderate in severity, occurring primarily during dose escalation.
    1 context sentence
    Summary · context
    we assigned 2539 adults with a body-mass index (BMI; the weight in kilograms divided by the square of the height in meters) of 30 or more, or 27 or more and at least one weight-related complication, excluding diabetes, in a 1:1:1:1 ratio to receive once-weekly, subcutaneous tirzepatide (5 mg, 10 mg,…
  6. 06HumanRandomized controlled trialSafety outcome

    In adults with obesity without diabetes, adverse events led to treatment discontinuation more often with tirzepatide 5, 10 and 15 mg than with placebo (for example 4.3% at 5 mg; no test reported).

    In plain wordsIn adults with obesity, a larger share of people stopped treatment because of side effects with tirzepatide than with placebo.

    Outcome
    IncreaseTreatment discontinuation due to adverse events
    Study

    n = 2,539

    Comparator
    Placebo
    Outcome group
    Adverse events · Whole body
    Studied dose
    5 mg, 10 mg or 15 mg once weekly · subcutaneous · 72 weeks, including a 20-week dose-escalation periodAs given in this study (human).

    Source sentences

    Summary
    Adverse events caused treatment discontinuation in 4.3%, 7.1%, 6.2%, and 2.6% of participants receiving 5-mg, 10-mg, and 15-mg tirzepatide doses and placebo, respectively.
    1 context sentence
    Summary · context
    we assigned 2539 adults with a body-mass index (BMI; the weight in kilograms divided by the square of the height in meters) of 30 or more, or 27 or more and at least one weight-related complication, excluding diabetes, in a 1:1:1:1 ratio to receive once-weekly, subcutaneous tirzepatide (5 mg, 10 mg,…

AI wrote and checked these results. AI can make mistakes, so check important results against the source.

Registered trials9

Trials this study reports on, or that list this study as a reference. Registry data from ClinicalTrials.gov.

9 trials · 4 ongoing · 3 not yet recruiting · 2 completed · 1 with posted results · source ClinicalTrials.gov (opens in a new tab)

Not yet recruitingPhase not statedNCT07099742

Effectiveness and Safety of Tirzepatide Among Participants With Obesity With or Without Type 2 Diabetes Mellitus (T2DM)

Dr. Md. Alimur Rezan = 364est. Nov 2026 to est. Dec 2027

Obesity

Not yet recruitingPhase 4NCT07756359

Tirzepatide for Ileal Pouch-anal Anastomosis (IPAA) and Chronic High Bowel Frequency (I8F-NS-X008)

University of North Carolina, Chapel Hilln = 20est. Sept 2026 to est. Sept 2027

Pouch, Ileal · Pouches, Ileoanal · Bowel Diseases, Inflammatory

Trial pageClinicalTrials.govUpdated 10 Aug 2026
RecruitingPhase not statedNCT07653412

Precision Obesity Medicine: Genetic Prediction of Response to GLP-1/GIP Agonists.

National and Kapodistrian University of Athensn = 22022 Apr 2026 to est. 30 Jun 2027

Obesity (Disorder) · Anti-obesity Agents · Precision Medicine

Trial pageClinicalTrials.govUpdated 10 Jul 2026
RecruitingNot applicableNCT07457437

Function and Lean Mass Preservation With Resistance Exercise During a GLP-1RA Treatment

University of Exetern = 60est. 1 Apr 2026 to est. 1 Dec 2027

Muscle Mass and Strength · Obesity & Overweight · Physical Function

Trial pageClinicalTrials.govUpdated 27 Mar 2026
Not yet recruitingPhase not statedNCT07504172

Real-world Effectiveness and Dosing Patterns of Tirzepatide in People With Obesity

Radboud University Medical Centern = 1,700est. 1 Apr 2026 to est. 1 Aug 2026

Overweight , Obesity · Obesity (Disorder)

Trial pageClinicalTrials.govUpdated 31 Mar 2026
CompletedPhase 2NCT06935838

Effects of Tirzepatide on Weight Loss and Chronic Inflammation in People With HIV

University of Hawaiin = 1212 Nov 2025 to 2 Jun 2026

Obesity and Overweight · HIV · Chronic Inflammation

RecruitingPhase 4NCT07154719

GLP-1R Actions on Muscle and the Skeleton

Pennington Biomedical Research Centern = 509 Oct 2025 to est. 1 May 2027

Musculoskeletal Abnormalities · Obesity · Sarcopenic Obesity · Osteoporosis · Drug Effect

Trial pageClinicalTrials.govUpdated 27 Aug 2026
RecruitingPhase 4NCT06606821

The Effects of Tirzepatide in People With Overweight/Obesity and Coronary Artery Disease

Tina Vilsbølln = 1241 Oct 2024 to est. 1 Aug 2028

Coronary Artery Disease · Coronary Microvascular Dysfunction · Overweight or Obesity · Stable Angina Pectoris · Chronic Coronary Artery Disease · Atherosclerosis Cardiovascular Disease

Trial pageClinicalTrials.govUpdated 22 May 2025
CompletedPhase 3Results postedNCT04184622

A Study of Tirzepatide (LY3298176) in Participants With Obesity or Overweight

Eli Lilly and Companyn = 2,5394 Dec 2019 to 6 Jul 2024

Overweight · Obesity

Trial pageClinicalTrials.govUpdated 24 Jul 2025

Version history

PepBank keeps every version of the data on this study. Status changes from Retraction Watch, Europe PMC and Crossref are listed with their source.

  1. Version 2Current

    9 Oct 2026, 12:39 UTC

    Study results updated

  2. Version 1

    9 Oct 2026, 03:07 UTC

    First added · source update from Europe PMC

Subjects

Terms as the source lists them.

PepBank is a research reference. Talk to a doctor before you use any peptide.