Expanded Access to REGN4461 for Patients With Diseases Associated With Deficient Leptin Signaling
Available (expanded access)
Conditions studied: Lipodystrophy, Generalized Lipodystrophy (GLD), Monogenic Obesity (MOB)
In brief
Provide Expanded Access to REGN4461 for patients with diseases associated with deficient leptin signaling.
Key facts
- Study ID
- NCT04710056
- Run by
- Regeneron Pharmaceuticals
- Last updated by the study team
- 2026-03-12
Who can join
Age: any. Sex: any. Healthy volunteers: not accepted.
Full record on ClinicalTrials.gov
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