Preserved supervised synthesis

Semaglutide synthesis · version 1

This URL preserves the exact reviewed public wording and source set for synthesis version 1.

Supervised synthesis pilot

What do selected human studies report about Semaglutide?

Manually reviewed August 18, 2026 · version 1

Browse all Human Evidence Reviews · Open preserved synthesis version 1 →

A bounded review of two sponsor-funded randomized trials: STEP 1 for weight change and SELECT for cardiovascular outcomes.12

Bottom line from this bounded source set

In the reviewed trials, semaglutide was associated with greater weight reduction than placebo in adults without diabetes, and fewer major cardiovascular events in adults with established cardiovascular disease and overweight or obesity without diabetes. The findings apply to those studied populations and trial conditions.12

Reviewed study record

STEP 1 weight-management trial

Design

A double-blind, randomized, placebo-controlled trial followed participants for 68 weeks alongside a lifestyle intervention.1

Population

The trial enrolled 1,961 adults with obesity, or overweight plus at least one weight-related condition, who did not have diabetes.1

Outcomes reported

Mean body-weight change at 68 weeks was -14.9% in the semaglutide group and -2.4% with placebo. Gastrointestinal events were common, and treatment discontinuation for gastrointestinal events was more frequent with semaglutide.1

Limitations

The sponsor-funded trial combined treatment with lifestyle intervention, excluded people with diabetes, and does not by itself establish outcomes after treatment stops.1

Reviewed study record

SELECT cardiovascular-outcomes trial

Design

A multicenter, double-blind, randomized, placebo-controlled, event-driven superiority trial assessed a composite of cardiovascular death, nonfatal myocardial infarction, or nonfatal stroke.2

Population

The trial enrolled 17,604 adults age 45 or older with established cardiovascular disease and overweight or obesity, but no history of diabetes.2

Outcomes reported

A primary cardiovascular event occurred in 6.5% of the semaglutide group and 8.0% of the placebo group; the reported hazard ratio was 0.80. Permanent discontinuation because of adverse events occurred in 16.6% and 8.2%, respectively.2

Limitations

The sponsor-funded findings apply to people with preexisting cardiovascular disease and without diabetes; they do not answer primary prevention for lower-risk populations.2

Reviewed source set

  1. PubMed · 33567185Once-Weekly Semaglutide in Adults with Overweight or Obesity ↗PubMed PMID 33567185 · EFetch XML reviewed 2026-08-18 · payload SHA-256 b3cf6a18c3906c27475c4a49d31f5741bf40fa056afc62f07d07fa54dbff28c4
    No registered Crossref update in the reviewed snapshotChecked August 19, 2026 for DOI 10.1056/nejmoa2032183. This bounded result is not proof that the publication has never been corrected or retracted. Open the pinned Crossref work endpoint ↗
  2. PubMed · 37952131Semaglutide and Cardiovascular Outcomes in Obesity without Diabetes ↗PubMed PMID 37952131 · EFetch XML reviewed 2026-08-18 · payload SHA-256 dabd7cd9d6c08b9c07da39a19d0b48266bfb7ddbbaacefe2e11025d105708245
    No registered Crossref update in the reviewed snapshotChecked August 19, 2026 for DOI 10.1056/nejmoa2307563. This bounded result is not proof that the publication has never been corrected or retracted. Open the pinned Crossref work endpoint ↗