Condition
Weight management
9 compounds were checked against weight management. 8 earned a graded row; the rest are named below.
Last updated
Recorded under Weight, alongside 4 other indications.
Compounds with a graded row
Ordered by rung, strongest first. The rung rates the study design; the chip beside it says what the study measured. Both are needed.
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Cagrilintide
human RCT Direct outcome In registered trials
- Who was studied
- adults with obesity, or overweight with at least one weight-related comorbidity; n=706, 26 weeks
A dose-finding phase 2 trial randomised participants to five cagrilintide doses, placebo, or liraglutide 3.0 mg, and measured change in body weight over 26 weeks. The evidence comes from a clinical population enrolled for obesity or overweight with a comorbidity, not from people in the healthy range managing their weight. Cagrilintide is not approved anywhere, alone or in combination.
Source PubMed 1 primary source read for this row
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Dulaglutide
human RCT Direct outcome Not approved for this condition
- Who was studied
- adults with type 2 diabetes inadequately controlled on metformin; n=1842, 52 weeks; neither BMI nor weight was an enrolment criterion
AWARD-11 measured change in body weight only as a secondary endpoint over 52 weeks; the primary endpoint was HbA1c and enrolment was by glycaemic control. The evidence comes from a diabetes population, not from healthy people managing weight, and no trial of dulaglutide selected for weight in people without diabetes is on file. Dulaglutide has no weight-management approval anywhere.
Source PubMed 1 primary source read for this row
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Exenatide
human RCT Direct outcome Not approved for this condition
- Who was studied
- obese women without diabetes, mean BMI 33.1, n=41, 35-week crossover with two 16-week treatment periods
A randomised double-blind placebo-controlled crossover study measured body weight change; mean loss was 2.49 kg on exenatide against a 0.43 kg gain on placebo. The evidence comes from obese women only — a clinical population, not people in the healthy range managing their weight — men were not enrolled, and no phase 3 weight programme for exenatide is on file.
Source PubMed 1 primary source read for this row
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Pramlintide
human RCT Direct outcome Not approved for this condition
- Who was studied
- obese adults not treated with insulin, mean BMI 37.8, 80 percent female; n=204, 16 weeks
A phase 2 randomised placebo-controlled dose-escalation study measured body weight and waist circumference over 16 weeks, with a placebo-corrected weight reduction of 3.7 percent. The evidence comes from a clinical population with a mean BMI of 37.8, not from people in the healthy range managing their weight. Pramlintide's approval is as a mealtime insulin adjunct in diabetes; the obesity programme did not proceed to registration and no weight-management approval is on file.
Source PubMed 1 primary source read for this row
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Semaglutide
human RCT Direct outcome Approved for this condition
- Who was studied
- adults with BMI >=30, or >=27 with at least one weight-related coexisting condition, without diabetes; n=1961, 68 weeks
STEP 1, a randomised double-blind placebo-controlled trial, measured percentage change in body weight over 68 weeks alongside lifestyle intervention, and the FDA approval is specifically for chronic weight management at those BMI thresholds. The evidence comes from a clinical population enrolled by BMI, not from people in the healthy range managing their weight; no trial below those thresholds is on file.
Source PubMed 1 primary source read for this row
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Tirzepatide
human RCT Direct outcome Approved for this condition
- Who was studied
- adults with BMI >=30, or >=27 with at least one weight-related complication, without diabetes; n=2539, 72 weeks
SURMOUNT-1, a phase 3 randomised placebo-controlled trial, measured percentage change in body weight at 72 weeks; the FDA approval for chronic weight management carries the same BMI thresholds as enrolment. The evidence comes from a clinical population enrolled by BMI, not from people in the healthy range managing their weight; participants with diabetes were studied separately in SURMOUNT-2.
Source PubMed 1 primary source read for this row
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VK2735
human RCT Direct outcome In registered trials
- Who was studied
- adults with BMI >=30, or >=27 with at least one weight-related comorbidity, BMI <50; n=176, 13 weeks
The VENTURE phase 2 trial of weekly subcutaneous VK2735 set percent change in body weight from baseline to week 13 as its primary outcome. The trial is short and small relative to the registrational obesity programmes, the evidence comes from a population enrolled by BMI rather than from people in the healthy range managing their weight, and no approval exists for any condition.
Source ClinicalTrials.gov 1 primary source read for this row
Checked, and nothing recorded
1 compound was checked against weight management and produced no gradeable row.
A compound is here because someone looked and the sources did not support a row — not because nobody looked. Under the rubric, uncertainty resolves to no row, and a row resting on a vendor page or a clinic blog is worse than no row at all.
What this page does not say
It reports what was measured, in whom, and how directly. It does not say what to take or at what dose, and a row here is a record of a study rather than a reason to use anything. Every rung links to the rubric that assigned it.