Semaglutide
Also called Ozempic (injection), Ozempic (tablets), Rybelsus, Wegovy (injection)
Research and education only. Not medical advice. Talk to a doctor.
In 30 seconds
A lab-made version of the gut hormone GLP-1, built to last about a week in the body.[1][4]
Tested in large trials, including one with more than 17,000 people.[14]
FDA-approved since 2017 for type 2 diabetes, weight management and heart risk.[5][7]
How far has the research gotten?
People in its biggest studies
How many people each study enrolled, as reported.Research over time
Papers on PubMed each year that mention Semaglutide.1,704 papers in 2025The label says Ozempic tablets and Rybelsus aren't interchangeable milligram for milligram.[2]
What studies used
What each paper reports. A record of published research, not a recommendation.The STEP 1 trial compared semaglutide with placebo for body-weight change in 1961 adults with overweight or obesity who did not have diabetes.
N Engl J Med · 2021 · PubMed 33567185What the paper reports
2.4 mg once weekly subcutaneously for 68 weeks, plus lifestyle intervention
Who: humanThe SUSTAIN-6 trial looked at cardiovascular death, heart attack and stroke with semaglutide versus placebo in 3297 people with type 2 diabetes.
N Engl J Med · 2016 · PubMed 27633186What the paper reports
0.5 mg or 1.0 mg once weekly for 104 weeks
Who: humanThe SELECT trial looked at major cardiovascular events with semaglutide versus placebo in 17,604 adults with existing cardiovascular disease and overweight or obesity but no diabetes.
N Engl J Med · 2023 · PubMed 37952131What the paper reports
2.4 mg once weekly subcutaneously (mean exposure 34.2 months)
Who: humanWhat the FDA label says
The label’s own dosing, so you can read the source. Not advice for you.Ozempic (semaglutide) injection
The label starts at 0.25 mg injected under the skin once weekly for 4 weeks, then raises the dose to 0.5 mg once weekly. If more glucose control is needed, the dose may go to 1 mg after at least 4 weeks at 0.5 mg, and then to 2 mg after at least 4 weeks at 1 mg; 2 mg once weekly is the stated maximum. For the chronic kidney disease indication, the label sets maintenance at 1 mg once weekly after at least 4 weeks at 0.5 mg. It is given on the same day each week, at any time of day with or without food, into the abdomen, thigh or upper arm, and a missed dose may be taken within 5 days.
Read the label on DailyMed (effective 2026-06-01) ›Rybelsus and Ozempic (semaglutide) tablets
Both tablets are taken by mouth once daily in the morning on an empty stomach with up to 4 ounces of plain water, swallowed whole, followed by a wait of at least 30 minutes before food, drinks or other oral medicines; the label says the two products are not interchangeable milligram for milligram. Rybelsus starts at 3 mg daily for days 1 to 30 (a starter dose the label says does not control glucose), goes to 7 mg daily for days 31 to 60, and from day 61 either stays at 7 mg or goes to 14 mg daily if more glucose control is needed. Ozempic tablets follow the same pattern at 1.5 mg daily for days 1 to 30, 4 mg daily for days 31 to 60, then either 4 mg or 9 mg daily. A missed tablet is skipped.
Read the label on DailyMed (effective 2026-01-30) ›Wegovy (semaglutide) injection
The injection is given under the skin of the abdomen, thigh or upper arm once weekly, starting at 0.25 mg for weeks 1 to 4 and stepping up every 4 weeks to 0.5 mg, 1 mg and 1.7 mg (weeks 13 to 16) before a maintenance dose from week 17. Maintenance per the label is 2.4 mg (recommended) or 1.7 mg weekly for cardiovascular risk reduction, for weight reduction in adults, and for weight reduction in children 12 and older; for adults who have tolerated 2.4 mg for at least 4 weeks and need more weight reduction, it may be raised to a maximum of 7.2 mg weekly. For MASH the label's maintenance dose is 2.4 mg weekly, reduced to 1.7 mg if not tolerated. If a step is not tolerated, the label suggests delaying escalation by 4 weeks.
Read the label on DailyMed (effective 2026-06-18) ›Wegovy (semaglutide) tablets
The tablet is taken by mouth once daily in the morning on an empty stomach with up to 4 ounces of plain water, swallowed whole, followed by a wait of at least 30 minutes before eating, drinking or taking other oral medicines. The label's schedule is 1.5 mg daily for days 1 to 30, 4 mg for days 31 to 60, 9 mg for days 61 to 90, and 25 mg daily from day 91 as maintenance for cardiovascular risk reduction and weight reduction in adults. If 25 mg is not tolerated, the label suggests considering a switch to the 1.7 mg weekly injection.
Read the label on DailyMed (effective 2026-06-18) ›What it is, in full 4
Semaglutide is a lab-made peptide modeled on the human hormone GLP-1, and it belongs to the GLP-1 receptor agonist drug class because it binds and switches on the GLP-1 receptor[1].
Compared with natural GLP-1 it has two swapped amino acids plus a fatty-acid chain attached at lysine 26, a design that strengthens binding to the blood protein albumin and stretches its action long enough for once-weekly injection[4].
Researchers at Novo Nordisk described how they designed and selected it in a 2015 paper, and Novo Nordisk is the labeler for its FDA-approved products[4][1].
Its label explains that it lowers blood sugar by boosting insulin release and damping glucagon release when glucose is elevated, along with a small slowing of stomach emptying right after meals[1].
Regulatory details 6
Ozempic injection (NDA 209637, original approval December 2017) is labeled for blood-sugar control in adults with type 2 diabetes, for lowering the risk of major cardiovascular events in adults with type 2 diabetes and established cardiovascular disease, and for lowering the risk of kidney decline, end-stage kidney disease and cardiovascular death in adults with type 2 diabetes and chronic kidney disease (labeled uses per source[1]).[5]
Checked 2026-10-06The oral semaglutide application (NDA 213051, original approval September 2019) now covers Rybelsus and Ozempic tablets, which are labeled for blood-sugar control in adults with type 2 diabetes and for lowering major cardiovascular event risk in adults with type 2 diabetes at high risk of such events (labeled uses per source[2]).[6]
Checked 2026-10-06Wegovy injection (NDA 215256, original approval June 2021) is labeled, alongside diet and activity, for cardiovascular risk reduction in adults with established cardiovascular disease and obesity or overweight, for long-term weight reduction in adults and in children 12 and older with obesity, and (under accelerated approval) for noncirrhotic MASH with F2 to F3 liver fibrosis in adults (labeled uses per source[3]).[7]
Checked 2026-10-06Wegovy tablets (NDA 218316, original approval December 2025) are labeled, alongside diet and activity, for cardiovascular risk reduction and long-term weight reduction in adults (labeled uses per source[3]).[8]
Checked 2026-10-06Semaglutide does not appear in Category 1, 2 or 3 of FDA's list of bulk drug substances nominated for 503A compounding (version updated May 14, 2026).[11]
Checked 2026-10-06Semaglutide is not named on the 2026 Prohibited List, but WADA's 2026 Monitoring Program includes markers of semaglutide in and out of competition, which means WADA is tracking use rather than prohibiting it (List checked at source[9]).[10]
Checked 2026-10-06Human trials on ClinicalTrials.gov
An intervention search for semaglutide on ClinicalTrials.gov returned 778 registered studies, the most advanced being phase 4 (119 studies tagged phase 4)[15].
All sources 15
- OZEMPIC (semaglutide) injection labelDailyMed (U.S. National Library of Medicine)
- RYBELSUS and OZEMPIC (oral semaglutide) tablets labelDailyMed (U.S. National Library of Medicine)
- WEGOVY (semaglutide) injection and tablets labelDailyMed (U.S. National Library of Medicine)
- Lau J et al. Discovery of the Once-Weekly Glucagon-Like Peptide-1 (GLP-1) Analogue Semaglutide. J Med Chem 2015PubMed
- Drugs@FDA record, NDA 209637 (Ozempic)U.S. FDA (openFDA)
- Drugs@FDA record, NDA 213051 (Rybelsus / Ozempic tablets)U.S. FDA (openFDA)
- Drugs@FDA record, NDA 215256 (Wegovy injection)U.S. FDA (openFDA)
- Drugs@FDA record, NDA 218316 (Wegovy tablets)U.S. FDA (openFDA)
- World Anti-Doping Code International Standard: Prohibited List 2026World Anti-Doping Agency
- The 2026 Monitoring ProgramWorld Anti-Doping Agency
- Bulk Drug Substances Nominated for Use in Compounding Under Section 503A (updated May 14, 2026)U.S. FDA
- Wilding JPH et al. Once-Weekly Semaglutide in Adults with Overweight or Obesity. N Engl J Med 2021PubMed
- Marso SP et al. Semaglutide and Cardiovascular Outcomes in Patients with Type 2 Diabetes. N Engl J Med 2016PubMed
- Lincoff AM et al. Semaglutide and Cardiovascular Outcomes in Obesity without Diabetes. N Engl J Med 2023PubMed
- ClinicalTrials.gov intervention search: semaglutideClinicalTrials.gov (U.S. National Library of Medicine)
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