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GLP-1 receptor agonist

Semaglutide

A once-weekly GLP-1 drug with large trials behind it. Roughly 15% average weight loss over 68 weeks in STEP 1.

By Cited Peptides Editorial Updated Medical review pending

This page has not yet been reviewed by a credentialed medical professional. It is educational and is not medical advice.

Why this evidence grade

FDA-approved

Approved for type 2 diabetes and chronic weight management, with large randomized trials including a cardiovascular outcomes trial.

What it is

Semaglutide is a modified version of the gut hormone GLP-1. It is sold as Ozempic (type 2 diabetes), Wegovy (weight management and cardiovascular risk reduction) and as an oral tablet (Rybelsus). It is by far the best-evidenced peptide on this site.

How it is thought to work

It activates GLP-1 receptors to increase insulin release when glucose is high, slow stomach emptying and reduce appetite through brain pathways. Engineered changes give it a half-life of about a week.

What the studies found10 studies explained

The STEP programme of randomized trials tested it for obesity; SUSTAIN-6 tested cardiovascular safety in type 2 diabetes and found fewer major cardiovascular events than placebo; later trials looked at kidney and heart outcomes. Head-to-head, tirzepatide produced greater weight loss than semaglutide in the SURMOUNT-5 trial.

Once-Weekly Semaglutide in Adults with Overweight or Obesity.

Wilding JPH, Batterham RL, Calanna S · N Engl J Med · 2021 · PMID 33567185

humanRandomized, double-blind, placebo-controlled phase 3 (STEP 1)

Who / how many
1,961 adults with overweight or obesity, no diabetes
What they found
Mean weight change at 68 weeks was -14.9% with semaglutide 2.4 mg vs -2.4% with placebo. About 86% lost at least 5% of body weight vs 32% on placebo.
Limitations
Funded by the manufacturer; participants also received lifestyle intervention; 68-week duration, so long-term outcomes need other trials.

Semaglutide and Cardiovascular Outcomes in Patients with Type 2 Diabetes.

Marso SP, Bain SC, Consoli A · N Engl J Med · 2016 · PMID 27633186

humanRandomized, double-blind, placebo-controlled phase 3 (SUSTAIN-6)

Who / how many
3,297 adults with type 2 diabetes, mostly with existing cardiovascular disease
What they found
Major cardiovascular events occurred in 6.6% on semaglutide vs 8.9% on placebo (hazard ratio 0.74).
Limitations
Designed mainly to show non-inferiority for safety; the population was high risk, and results do not apply to everyone.

Tirzepatide as Compared with Semaglutide for the Treatment of Obesity.

Aronne LJ, Horn DB, le Roux CW · N Engl J Med · 2025 · PMID 40353578

humanOpen-label phase 3b head-to-head

Who / how many
751 adults with obesity, no diabetes
What they found
At 72 weeks, tirzepatide produced -20.2% weight change vs -13.7% for semaglutide.
Limitations
Open-label (not blinded), maximum tolerated doses, and funded by the maker of tirzepatide.

Semaglutide and Cardiovascular Outcomes in Obesity without Diabetes.

Lincoff AM, Brown-Frandsen K, Colhoun HM · N Engl J Med · 2023 · PMID 37952131

humanRandomized, double-blind, placebo-controlled phase 3 (SELECT)

Who / how many
17,604 adults aged 45+ with cardiovascular disease and overweight or obesity, no diabetes (8,803 semaglutide, 8,801 placebo)
What they found
Semaglutide 2.4 mg weekly was superior to placebo at reducing a composite of cardiovascular death, nonfatal heart attack or nonfatal stroke over a mean follow-up of about 40 months. A related report describes this as a 20% reduction in major cardiovascular events.
Limitations
Funded by Novo Nordisk. Participants already had cardiovascular disease, so the result may not apply to people without it.

Long-term kidney outcomes of semaglutide in obesity and cardiovascular disease in the SELECT trial.

Colhoun HM, Lingvay I, Brown PM · Nat Med · 2024 · PMID 38796653

humanPrespecified analysis of a randomized trial (SELECT kidney outcomes)

Who / how many
About 17,600 adults with overweight/obesity and cardiovascular disease, no diabetes
What they found
The main composite kidney endpoint occurred in 1.8% on semaglutide vs 2.2% on placebo (hazard ratio 0.78). Kidney function (eGFR) declined more slowly with semaglutide.
Limitations
Kidney outcomes were a secondary analysis, event rates were low, and the trial was manufacturer funded.

Weight regain and cardiometabolic effects after withdrawal of semaglutide: The STEP 1 trial extension.

Wilding JPH, Batterham RL, Davies M · Diabetes Obes Metab · 2022 · PMID 35441470

humanExploratory off-treatment extension of a randomized trial (STEP 1)

Who / how many
327 participants from the STEP 1 trial
What they found
After stopping semaglutide and lifestyle support, people regained 11.6 percentage points of their lost weight within a year, about two-thirds of the loss, and cardiometabolic improvements reverted towards baseline.
Limitations
Exploratory analysis in a subset of the original trial. Suggests that treatment may need to continue to keep the benefit.

Once-Weekly Semaglutide in Adolescents with Obesity.

Weghuber D, Barrett T, Barrientos-Pérez M · N Engl J Med · 2022 · PMID 36322838

humanRandomized, double-blind, placebo-controlled trial (STEP TEENS)

Who / how many
201 adolescents aged 12 to <18 with obesity or overweight with a comorbidity
What they found
BMI changed by -16.1% with semaglutide 2.4 mg vs +0.6% with placebo over 68 weeks. 73% of the semaglutide group lost at least 5% of weight. Gallstones were more common with semaglutide, and serious adverse events occurred in 11% vs 9%.
Limitations
Funded by Novo Nordisk. Adolescents only; 68 weeks, so long-term effects on growth and development are unknown.

Semaglutide versus dulaglutide once weekly in patients with type 2 diabetes (SUSTAIN 7): a randomised, open-label, phase 3b trial.

Pratley RE, Aroda VR, Lingvay I · Lancet Diabetes Endocrinol · 2018 · PMID 29397376

humanOpen-label phase 3b head-to-head (SUSTAIN 7)

Who / how many
Adults with type 2 diabetes on metformin
What they found
Semaglutide was superior to dulaglutide at both doses for lowering HbA1c and body weight at week 40, with a similar safety profile.
Limitations
Open-label, 40 weeks, and funded by Novo Nordisk.

Once-Weekly Semaglutide in Persons with Obesity and Knee Osteoarthritis.

Bliddal H, Bays H, Czernichow S · N Engl J Med · 2024 · PMID 39476339

humanRandomized, double-blind, placebo-controlled phase 3 (STEP 9)

Who / how many
407 adults with obesity and moderate knee osteoarthritis
What they found
Semaglutide 2.4 mg produced greater weight loss and greater reductions in knee osteoarthritis pain than placebo over 68 weeks. More participants stopped treatment because of adverse events with semaglutide (6.7% vs 3.0%), mainly gastrointestinal.
Limitations
Manufacturer-funded; pain is self-reported, and weight loss itself may explain much of the pain reduction.

Long-Term Efficacy and Safety of Once-Weekly Semaglutide for Weight Loss in Patients Without Diabetes: A Systematic Review and Meta-Analysis of Randomized Controlled Trials.

Moiz A, Levett JY, Filion KB · Am J Cardiol · 2024 · PMID 38679221

reviewSystematic review and meta-analysis

Who / how many
4 randomized trials, 3,087 adults with overweight/obesity and no diabetes
What they found
Semaglutide 2.4 mg weekly lowered body weight by an average of about 12 percentage points more than placebo over at least 68 weeks. Gastrointestinal events were more common (relative risk 1.47) but mostly mild to moderate and transient.
Limitations
Only four trials, all of similar design and mostly manufacturer funded.

More published research (summaries coming)

Clinical trials24 registered

24 trials on ClinicalTrials.gov list Semaglutide as an intervention; the most advanced are shown. Registration is not evidence of benefit: many trials are ongoing, unpublished or never reported results.

TrialPhaseStatusnSponsor
A Research Study to Look at How Semaglutide Compared to Placebo Affects Diabetic Eye Disease in People With Type 2 Diabetes
NCT03811561
Phase 3active not recruiting1500Novo Nordisk A/S
Maridebart Cafraglutide Versus Semaglutide in Participants With Type 2 Diabetes
NCT07866066
Phase 3not yet recruiting1300Amgen
Efficacy and Safety of Ribupatide Administered Once Weekly Compared With Semaglutide and Placebo in Participants Living With Obesity Who Do Not Have Diabetes
NCT07284979
Phase 3active not recruiting1270Kailera
A Research Study on How Well Cagrilintide and CagriSema Work in Children and Adolescents With Excess Body Weight
NCT07253285
Phase 3recruiting460Novo Nordisk A/S
A Research Study on How Well Semaglutide Helps Children and Teenagers With Excess Body Weight Lose Weight
NCT05726227
Phase 3active not recruiting212Novo Nordisk A/S
Research Study on How People With Type 2 Diabetes Tolerate Switching From Semaglutide to Cagrisema
NCT07817251
Phase 3recruiting210Novo Nordisk A/S
A Research Study to See How Much CagriSema Lowers Blood Sugar and Body Weight Compared to Placebo in People With Type 2 Diabetes Treated With Diet and Exercise
NCT06323174
Phase 3completed189Novo Nordisk A/S
Semaglutide in Women With Polycystic Ovary Syndrome and Obesity
NCT06896981
Phase 2 / PHASE3completed31Bangabandhu Sheikh Mujib Medical University, Dhaka, Bangladesh
A Study to Compare Different Doses of RO7795081 With Placebo or Semaglutide in People With Type 2 Diabetes
NCT07112872
Phase 2active not recruiting330Hoffmann-La Roche
A Research Study Comparing How Well Different Doses of the Medicine UBT251 Lower Blood Sugar in People With Type 2 Diabetes
NCT07668388
Phase 2recruiting300Novo Nordisk A/S

Data pulled from the ClinicalTrials.gov API. Check sponsors: several newer peptide registrations come from companies that also sell the product.

European research

5,188 records in Europe PMC mention Semaglutide in the title or abstract. Of the 25 most-cited with European author affiliations that we sampled, the most common countries were Denmark (17), United Kingdom (7), UK (7), Germany (5).

Search the EU registers directly: EU Clinical Trials Register (pre-2023 trials), CTIS (trials since 2022) and the EMA medicines database.

Side effects and risks

Gastrointestinal effects (nausea, vomiting, diarrhea, constipation) are the most common and mostly occur during dose escalation. Weight is typically regained after stopping. Other known risks listed on labelling include gallbladder problems and pancreatitis; consult prescribing information for the full list.

United StatesFDA-approved prescription drug (Ozempic, Wegovy, Rybelsus). Compounded versions are a separate and contested area; check FDA guidance.
CanadaHealth Canada-authorized prescription drug (Ozempic, Wegovy, Rybelsus).
European UnionEMA-authorized (centrally authorized as Ozempic, Wegovy and Rybelsus). Prescription-only.
Sport (WADA)Not prohibited in sport.

Last verified . FDA Drugs@FDA database.

Common questions

How much weight do people lose on semaglutide?

In the STEP 1 trial, average weight change was -14.9% at 68 weeks vs -2.4% with placebo, alongside lifestyle intervention.

What happens when you stop?

The STEP 1 extension found participants regained much of the lost weight after stopping treatment.

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