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Semaglutide in Comorbid Schizophrenia Spectrum Disorder and Obesity
Sponsor: Centre for Addiction and Mental Health
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
Conditions
Interventions
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
Placebo
Placebo will be provided to participants
Locations (1)
Centre for Addiction and Mental Health
Toronto, Ontario, Canada