Congenital generalized lipodystrophy
MONDO:0006536An extremely rare autosomal recessive condition, characterized by an extreme scarcity of fat in the subcutaneous tissues.
Also known as: congenital generalised lipodystrophy (disease), congenital generalized lipodystrophy, congenital generalized lipodystrophy (disease), familial generalised lipodystrophy, familial generalized lipodystrophy, hereditary generalised lipodystrophy, hereditary generalized lipodystrophy, lipodystrophy, congenital generalised
4 clinical trials for this condition and its sub-types.
Follow this condition — get notified about new trialsSub-types
Broader categories
-
Rare leptin disorder patients gain access to experimental drug
Disease control AVAILABLEThis program provides expanded access to REGN4461 (mibavademab) for people with rare diseases caused by deficient leptin signaling, such as generalized lipodystrophy and monogenic obesity. The drug aims to help control metabolic issues linked to these conditions. Participants rec…
Sponsor: Regeneron Pharmaceuticals • Aim: Disease control
Last updated Jun 27, 2026 11:00 UTC
-
Massive european registry launches to unlock secrets of rare fat disorder
Knowledge-focused Recruiting nowThis study is a European registry for people with lipodystrophy, a rare condition where the body loses or lacks fat tissue. Researchers will follow up to 5,000 patients over time, collecting health data and genetic information. The goal is to better understand the disease, its pr…
Sponsor: University of Ulm • Aim: Knowledge-focused
Last updated Jun 27, 2026 08:01 UTC