Educational reference only — not medical advice. Nothing is sold on this site. Research compounds are not for human use.
Home>>Peptides>>Semaglutide
Approved medicineGLP-1 / incretin

Semaglutide

A long-acting GLP-1 receptor agonist approved in injectable form for type 2 diabetes (Ozempic) and chronic weight management (Wegovy), and in oral form (Rybelsus). It is among the most extensively studied molecules in the peptide space.

CompoundSemaglutide
CategoryGLP-1 receptor agonist
ClassGLP-1 and Incretin Therapies
Evidence tierApproved medicine
WADA statusNot individually listed; verify current status if subject to testing
Sold on this siteNo — this is a reference database

Overview

This entry covers Semaglutide, a glp-1 receptor agonist, graded "Approved medicine" in this catalog's evidence system. This compound exists as an approved medicine in at least one major jurisdiction. Approval applies to specific, labeled indications and to the regulated product — not to compounded or research-grade copies.

A long-acting GLP-1 receptor agonist approved in injectable form for type 2 diabetes (Ozempic) and chronic weight management (Wegovy), and in oral form (Rybelsus). It is among the most extensively studied molecules in the peptide space.

Mechanism of Action

Semaglutide mimics endogenous GLP-1: it enhances glucose-dependent insulin secretion, suppresses inappropriate glucagon release, slows gastric emptying, and acts on central appetite circuits to reduce hunger and energy intake. An attached C18 fatty-diacid chain promotes albumin binding, extending its half-life to roughly one week and allowing once-weekly injection.

Research and Evidence

The STEP 1 randomized trial (n=1,961) reported a mean body-weight reduction of 14.9% with once-weekly semaglutide 2.4 mg versus 2.4% with placebo over 68 weeks. Large cardiovascular outcome trials in type 2 diabetes have additionally supported cardiometabolic benefit.

Evidence in context: the GLP-1 and Incretin Therapies class page collects the shared evidence themes and study-reading guidance for this category.

Safety and Side Effects

The most common adverse effects are gastrointestinal — nausea, vomiting, diarrhea, and constipation — and are often dose-related. Labeled warnings include gallbladder disease, pancreatitis, and, in patients with type 2 diabetes, retinopathy complications. It is contraindicated in individuals with a personal or family history of medullary thyroid carcinoma or MEN2.

Educational notice: this entry describes published research and, where they exist, regulator labels. It is not medical advice and not a recommendation for use. Research-grade compounds have no verified human-safety data.

Frequently Asked Questions

What is the evidence tier of Semaglutide?

Semaglutide is graded "Approved medicine" on this site. This compound exists as an approved medicine in at least one major jurisdiction. Approval applies to specific, labeled indications and to the regulated product — not to compounded or research-grade copies.

Is Semaglutide an approved medicine?

Semaglutide exists as an approved medicine in at least one major jurisdiction — but approval covers the regulated product and its labeled indications only. Compounded or research-grade versions of the same molecule are not the approved product.

Where can I read the primary studies for Semaglutide?

The references section at the end of this entry links the key primary sources — regulator labels, trial registrations, and peer-reviewed papers. Our "How to Read a Peptide Study" guide explains how to evaluate them.

References

  1. Wilding JPH, et al. Once-Weekly Semaglutide in Adults with Overweight or Obesity (STEP 1). N Engl J Med 2021. [source]
  2. Drucker DJ. Mechanisms of Action and Therapeutic Application of Glucagon-Like Peptide-1. Cell Metab 2018. [source]
  3. ClinicalTrials.gov — registered semaglutide studies. [source]
EM
Dr. Elena Marsh, PhDMolecular Pharmacology · Lead Editor

Written and maintained by the editorial team. Medically reviewed by Dr. James Okafor, MD (Internal Medicine).

Evidence tier: Approved medicine · Last reviewed: 2026-09-05 · Sources cited below.

Advertisement