Trials / NCT05194124
Phase 3 Crossover Trial of Two Formulations of Setmelanotide in Participants With Specific Gene Defects in the MC4R Pathway
Completed Phase 3 Drug / neuroprotection
- Sponsor
- Rhythm Pharmaceuticals, Inc.
- Treatment
- Setmelanotide 2 mg; Setmelanotide 2.5 mg; Setmelanotide 3 mg; Setmelanotide 20 mg; Setmelanotide 25 mg; Setmelanotide 30 mg
- Gene
- Not stated
- Conditions
- Bardet-Biedl Syndrome, POMC Deficiency
- Ages
- 6 Years to no upper limit
- Enrollment
- 19 participants
- Started
- 2021-12-21
- Main results expected
- 2023-10-19
- Results posted
- Yes
- Record last updated
- 2024-11-26
What the study is testing
A trial to compare the weekly and daily formulations of setmelanotide in participants with genetic defects in the melanocortin-4 receptor pathway.
Where it runs
Canada (1)
- Alberta Health Services, Edmonton, Alberta
Germany (1)
- Charité - Universitätsmedizin Berlin, Campus Virchow-Klinikum, Berlin
Netherlands (1)
- Erasmus MC, Rotterdam
Puerto Rico (1)
- UPR Medical Sciences Campus, Rio Piedras
United Kingdom (1)
- Addenbrooke's Hospital, Cambridge
United States (2)
- Honor Health Research Institute, Scottsdale, Arizona
- Marshfield Clinic Research Institute, Marshfield, Wisconsin