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ACTIVE NOT RECRUITING
NCT05333003
NA

Semaglutide in Comorbid Schizophrenia Spectrum Disorder and Obesity

Sponsor: Centre for Addiction and Mental Health

View on ClinicalTrials.gov

Summary

Rates of obesity in patients with schizophrenia-spectrum disorder (SSD)s have reached epidemic proportions, with established contributing effects of antipsychotic (AP) medications. Among agents approved for chronic weight management, glucagon-like peptide-1 receptor agonists (GLP-1RA) are associated with reductions in cardiovascular mortality, with recent FDA approval for once weekly semaglutide for this indication. This study will investigate whether semaglutide is effective in reducing body weight in overweight or obese individuals with SSDs who are on APs and do not demonstrate adequate weight loss on metformin (the first line treatment for weight loss in SSDs).

Official title: Semaglutide in Comorbid Schizophrenia Spectrum Disorder and Obesity for Metformin Non-responders: a Single-blind Randomized Control Trial

Key Details

Gender

All

Age Range

18 Years - 70 Years

Study Type

INTERVENTIONAL

Enrollment

92

Start Date

2022-05-25

Completion Date

2026-08

Last Updated

2026-05-27

Healthy Volunteers

No

Interventions

DRUG

Semaglutide

The semaglutide dose will start with 0.25 mg/week, and slowly increased every four weeks as tolerated up to a maximal dose of 2 mg/week

OTHER

Placebo

Placebo will be provided to participants

Locations (1)

Centre for Addiction and Mental Health

Toronto, Ontario, Canada