Danish GOAL trial to test semaglutide in adolescents on antipsychotics
The single-arm, open-label feasibility study will enroll 34 patients aged 12 to 18 with obesity at Copenhagen University Hospital, Bispebjerg.
PR
By Priya Raman · Science Reporter
Sep 16 20:00 ETSource: BMJ open
The wire
- 01Participants on stable antipsychotic treatment will receive once-weekly subcutaneous semaglutide up to 2.4 mg for 36 weeks alongside standard care, followed by 18 months of observational follow-up.
- 02Targets a group with antipsychotic-associated obesity and limited evidence-based options; secondary outcomes include BMI SD score, body composition, metabolic biomarkers and psychiatric outcomes.
- 03The primary outcome is study completion rate, not weight loss; the design is single-arm and uncontrolled and is intended only to inform a later randomised trial.
From the source
Read at pubmed.ncbi.nlm.nih.govSemaglutide as adjunct treatment for obesity in adolescents receiving antipsychotic medication (the GOAL trial): protocol for a single-arm, open-label feasibility study
BMJ open · 2026 Sep 17 · Giraldi LV, Andersen JT, Jespersen J et al.
Source URL https://pubmed.ncbi.nlm.nih.gov/42754274/