Semaglutide is a GLP-1 receptor agonist — it binds to and activates the same receptors as glucagon-like peptide 1, a hormone your gut releases in response to food. By mimicking GLP-1, semaglutide signals the pancreas to release insulin in a glucose-dependent manner (reducing the risk of hypoglycemia compared to older diabetes drugs), slows the rate at which food moves from the stomach into the intestine, and acts on brain areas that regulate appetite and satiety.
Ozempic was the first version approved, indicated for improving blood sugar control in adults with type 2 diabetes and, importantly, for reducing major cardiovascular events in adults with type 2 diabetes and established cardiovascular disease. Wegovy, approved later at a different pen strength range, is indicated specifically for chronic weight management.
The SELECT cardiovascular outcomes trial (2023) was a landmark: it demonstrated that semaglutide reduced the risk of heart attack, stroke, and cardiovascular death in people with obesity but without diabetes — the first GLP-1 medication to demonstrate this benefit in a non-diabetic population, substantially expanding the evidence base for the drug class.
Ozempic is available in 0.5 mg, 1 mg, and 2 mg pens. Wegovy is available in its own pen strength range for the weight management indication.
Both Ozempic and Wegovy carry an FDA black box warning for thyroid C-cell tumors based on animal studies. They are contraindicated in patients with a personal or family history of medullary thyroid carcinoma (MTC) and in patients with Multiple Endocrine Neoplasia syndrome type 2 (MEN2).
More CV outcome data than any GLP-1: Semaglutide has the most extensive published cardiovascular outcomes data in the class, including SELECT (non-diabetic obesity), SUSTAIN-6, and SOUL trial results. This is a meaningful advantage for patients where cardiovascular risk is a primary concern.