RP Cure Tracker

Trials / NCT07674290

Real-World Effects of MC4R Agonist Therapy in BBS and Severe Genetic Obesity

Recruiting now Phase 4 Drug / neuroprotection

Sponsor
Tom Hühne
Treatment
Setmelanotide
Gene
Not stated
Conditions
Bardet Biedl Syndrome (BBS), Bardet Biedl Syndrome, Bardet-Biedl Syndrome (BBS), Alstrom Syndrome
Ages
Any to no upper limit
Enrollment
200 participants
Started
2023-01-01
Main results expected
2030-12-31
Results posted
Not yet
Record last updated
2026-06-29

What the study is testing

Bardet-Biedl syndrome (BBS) and other rare disorders associated with impairment of the melanocortin-4 receptor (MC4R) pathway are characterized by severe early-onset obesity, hyperphagia, and substantial morbidity. Setmelanotide, an MC4R agonist, is approved in Europe for selected genetic obesity disorders and reimbursed in Germany for eligible patients. This study aims to evaluate the effectiveness, safety, treatment persistence, metabolic outcomes, and patient-reported outcomes of Setmelanotide under real-world conditions. The registry is designed to allow future inclusion of additional MC4R agonists as they become approved and clinically available. The study will primarily be conducted at University Hospital Essen and will collect longitudinal routine clinical data from pediatric and adult patients receiving MC4R agonist therapy according to approved indications.

Where it runs

Germany (1)

Open on ClinicalTrials.gov for contacts and eligibility