Obesity

Efficacy and safety of semaglutide 2.4 mg according to antidepressant use at baseline: A post hoc subgroup analysis

Obesity (Silver Spring)Published Post hoc subgroup analysis of the STEP 1-3 and 5 randomised trials

Authors' conclusion

In adults with overweight/obesity, semaglutide provided clinically meaningful weight loss regardless of baseline AD use, with an AE profile consistent with previous studies.

Study context

Population
Adults with overweight/obesity (and T2D in STEP 2 only), STEP 1–3 and 5; excluded severe major depressive disorder within 2 years or PHQ-9 score ≥15; subgroups by baseline antidepressant use (on/off)539 on antidepressants
Participants
3,683 adults
Comparison
Semaglutide 2.4 mg vs placebo, by baseline antidepressant use
Primary endpoint
Mean body weight change from baseline
Follow-up
Week 68
Methodological detailsexploratory, placebo-controlled
  • Exploratory
  • Placebo-controlled

Primary result

As reported in the abstract

Body weight change from baseline, STEP 1

STEP 1, on antidepressants: semaglutide vs placebo

−15.7% vs −0.2%

STEP 1, not on antidepressants: semaglutide vs placebo

−14.7% vs −2.8%

Safety

Adverse events, participants on antidepressants

Prevalence of adverse events (AEs) generally similar between semaglutide and placebo in participants on antidepressants at baseline

Original publication

Efficacy and safety of semaglutide 2.4 mg according to antidepressant use at baseline: A post hoc subgroup analysis. Obesity (Silver Spring). Published 21 November 2023. doi:10.1002/oby.23946

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