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Semaglutide

GLP-1 receptor agonist for weight loss and type 2 diabetes management

Semaglutide molecular structure

Overview

Semaglutide is a medication that mimics GLP-1, a hormone your gut naturally releases after eating. It's the active ingredient in brand names you may have heard: Ozempic (for diabetes) and Wegovy (for weight loss). **How does it work?** When you eat, your body releases GLP-1 to signal fullness. Semaglutide does the same thing, but much more powerfully and for much longer. It tells your brain you're satisfied, slows down how fast food leaves your stomach, and helps your pancreas release insulin more effectively. **What the research shows:** • FDA-approved for type 2 diabetes and chronic weight management • Clinical trials show average weight loss of 15-17% of body weight • Reduces risk of heart attacks, strokes, and cardiovascular death • May protect kidneys in people with diabetes • Emerging research suggests potential brain-protective benefits **Available forms:** Weekly injection (Ozempic, Wegovy) or daily oral tablet (Rybelsus) **Common side effects:** Nausea, especially when starting — usually improves over time. Your doctor will typically start you on a low dose and gradually increase it. --- **Sources:** Ghusn W, et al. (2023) Healthcare. DOI:10.3390/healthcare13222922 | Müller TD, et al. (2023) Biomolecules. DOI:10.3390/biom15111574 | Clinical trial data from STEP and SUSTAIN programs

Last reviewed: 2026-08-18

Identity & Aliases

Also known as

Ozempic (type 2 diabetes brand)Wegovy (obesity brand)GLP-1 receptor agonistSemaglutide sodium
CAS910463-68-2
PubChem56843331

Full composition (formula, molecular weight, sequence) in Quick Facts →

Research Areas

Type 2 diabetesObesity and weight managementCardiovascular risk reductionNon-alcoholic steatohepatitis (investigational)Heart failure (investigational)

Available Evidence

Human

Semaglutide is FDA-approved (Ozempic 2017 for type 2 diabetes; Wegovy 2021 for obesity; 2024 for cardiovascular risk reduction in adults with overweight/obesity and established CVD). STEP 1 reported ~14.9% mean weight loss at 68 weeks; SELECT (n=17,604) showed a 20% reduction in major adverse cardiovascular events.

Animal

Rodent and primate studies established GLP-1-mediated weight loss and glycemic effects.

In Vitro

Cell-based studies characterize GLP-1 receptor agonism, glucose-stimulated insulin secretion and appetite signaling.

Uncertain

Long-term effects beyond trial durations, real-world persistence, muscle-loss concerns during weight loss, and the clinical importance of GI adverse events (nausea, gallbladder events) continue to be studied.

Key Studies & Findings

3 studies
Clinical2024

FDA approved the expanded indication for Wegovy to reduce cardiovascular risk in adults with known heart disease and overweight or obesity.

Benefits & Effects

13 documented

Significant weight loss

clinical

Blood sugar control

clinical

Reduced cardiovascular risk

clinical

Appetite suppression

clinical

Improved insulin sensitivity

clinical

GLP-1 agonist

Significant weight loss

Blood sugar control.

Weight Loss: -14.9% to -17.3% body weight (STEP trials)

clinical

CV Outcomes: 20% MACE reduction (HR 0.80)

clinical

GLP-1 agonist

Significant weight loss

Blood sugar control.

Side Effects & Safety

20 reported

Interaction

Avoid: DPP-4 inhibitors

Constipation

MildUncommon

Nausea

MildUncommon

Diarrhea

MildUncommon

Rare pancreatitis or thyroid risk

SevereRare

Interaction

Avoid: DPP-4 inhibitors

GI adverse events

Moderate

Discontinuation (GI)

Mild

Serious AEs

Mild

Pancreatitis risk

Mild

Thyroid cancer risk

Mild

Mild-Moderate side effect

Mild-ModerateVery common (44%) Reversible

Onset: Days

Management: Slow titration, small meals

Dose-dependent

Mild-Moderate side effect

Mild-ModerateVery common (30%) Reversible

Onset: Days

Management: Hydration, dose adjustment

Dose-dependent

Mild-Moderate side effect

Mild-ModerateCommon (24%) Reversible

Onset: Days

Management: Antiemetics, hydration

Dose-dependent

Mild-Moderate side effect

Mild-ModerateCommon (24%) Reversible

Onset: Days

Management: Fiber, fluids

Dose-dependent

Mild-Moderate side effect

Mild-ModerateCommon (20%) Reversible

Onset: Days

Management: Rule out pancreatitis

Dose-dependent

Mild side effect

MildCommon (1-4 bpm) Reversible

Onset: Weeks

Management: Monitor; discontinue if sustained

Dose-dependent

Moderate-Severe side effect

Moderate-SevereUncommon (1.6%) Reversible

Onset: Weeks-months

Management: Gallbladder studies

Dose-dependent

Severe side effect

SevereRare (0.2%) Reversible

Onset: Variable

Management: DISCONTINUE immediately

Severe side effect

SevereUnknown in humans

Onset: Unknown

Management: CONTRAINDICATED with MTC/MEN2

Dose-dependent

Limitations & Open Questions

GI side effects (nausea, vomiting, diarrhea) are common; rare but serious events (pancreatitis, gallbladder disease; thyroid C-cell tumors in rodents) warrant caution; high cost and access barriers; weight regain typically follows discontinuation; long-term safety beyond 2-4 years is still accruing.

Pharmacology

GLP-1 receptor agonist with once-weekly subcutaneous dosing (Ozempic/Wegovy; an oral formulation exists for type 2 diabetes). Elimination half-life is approximately 1 week (steady state in ~4-5 weeks). Dose titration is used to reduce GI intolerance.

Reported Research Dosing

Reported values from research literature and community protocols. Educational reference only — not a dosing recommendation or medical advice.

0.25-2.4 mg Weekly

Route: SC
Half-life: ~7 days

Research Protocols

Weight Loss Initiation

Dose
0.25mg
Frequency
Weekly x 4 weeks, then increase
Route
Subcutaneous

Weight Loss Maintenance

Dose
2.4mg
Frequency
Weekly (after 16-week titration)
Route
Subcutaneous

Diabetes Management

Dose
0.5-1mg
Frequency
Weekly
Route
Subcutaneous

Cardiovascular Protection

Dose
0.5-1mg
Frequency
Weekly
Route
Subcutaneous

Tolerability-Based

Dose
0.25-2.4mg
Frequency
Weekly (individualized)
Route
Subcutaneous

Research protocols are for educational purposes only. Always consult qualified medical professionals.

Frequently Asked Questions

What is the difference between Ozempic and Wegovy?

Same active drug (semaglutide); Ozempic is approved for type 2 diabetes (doses up to 2 mg), Wegovy for chronic weight management (2.4 mg) and cardiovascular risk reduction.

Do you regain weight after stopping semaglutide?

Trials show substantial weight regain after discontinuation; weight management is typically considered chronic therapy.

Research Citations

3
Safety of Semaglutide.

Smits MM, Van Raalte DH (2021)

4
Semaglutide for the treatment of obesity.

Chao AM, Tronieri JS, Amaro A, Wadden TA (2023)

5
Semaglutide 2·4 mg once a week in adults with overweight or obesity, and type 2 diabetes (STEP 2): a randomised, double-blind, double-dummy, placebo-controlled, phase 3 trial.

Davies M, Færch L, Jeppesen OK, Pakseresht A, Pedersen SD, Perreault L, Rosenstock J, Shimomura I, Viljoen A, Wadden TA, Lingvay I, STEP 2 Study Group (2021)

+ 21 more citations

Related Resources

Quick Facts

Formula

C187H291N45O59

Molecular Weight

4113.58

Sequence

MKSIYFVAGLFVMLVQGSWQRSLQDTEEKSRSFSASQADPLSDPDQMNEDKRHSQGTFTSDYSKYLDSRRAQDFVQWLMNTKRNRNNIAKRHDEFERHAEGTFTSDVSSYLEGQAAKEFIAWLVKGRGRRDFPEEVAIVEELGRRHADGSFSDEMNTILDNLAARDFINWLIQTKITDRK

Mechanism

GLP-1 receptor agonist that regulates appetite and glucose metabolism

Safety Information

FDA approved for diabetes and obesity. Common side effects include nausea, vomiting, and diarrhea.

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