The Effect of GLP-1 Agonist in Patients With Hypothalamic Obesity: Prospective, Pilot Study
NCT06217848 · Unknown status
Last updated 2026-05-28This clinical trial tests whether a GLP-1 agonist can help reduce weight in adults with hypothalamic obesity caused by conditions like panhypopituitarism or craniopharyngioma.
What this study is testing ClinicalTrials.gov NCT06217848 ↗
Description as written by the study sponsor.
GLP-1 analogs are used as agents in the existing treatment of obesity. However, there are lack of previous reports on the effectiveness and role of GLP-1 analogs in the development of obesity traits in patients with functionally impaired hypothalamus. With this preliminary study, the investigators would explore the role of GLP-1 analogues to identify eating behavioral pathology subtype differences in the therapeutic efficacy of GLP-1 analogues in hypothalamic obesity patients. This will allow us to identify the role of specific nuclei which could be the pathogenesis of hypothalamic obesity. Our hypotheses: GLP-1 analogs will effectively induce weight loss in patients with hypothalamic obesity, and different subtypes of hypothalamic obesity will respond differently to GLP-1 analogs.
Treatments tested
- Saxenda Drug
Patients will receive subcutaneous injections of Saxenda 18 mg/3 mL Pen (liraglutide\_obesity) starting at 0.6 mg qd. Increase by 0.6 mg qd at weekly intervals to 1.2 mg qd in week 2, 1.8 mg qd in week 3, 2.4 mg qd in week 4, 3.0 mg qd in week 5, and maintain for 8 weeks at a maximally tolerated dose within 3.0 mg starting in week 5. If the subject's response to treatment does not allow for escalation to the planned dose, subjects will inject an adaptive maximally tolerated dose within the planned dose at each cycle. Total duration of Saxenda treatment is 12 weeks.
| Main thing measured | Change in weight |
|---|---|
| Sponsor | Seoul National University Hospital |
| Conditions studied | Panhypopituitarism, Craniopharyngioma, Hypothalamic Obesity |
| GLP-1 drugs | — |
Full protocol, eligibility, and contacts on ClinicalTrials.gov NCT06217848 ↗