Study design & results
Available in the Gosset platform where reported.
Trial intelligence / Profile preview
NCT05194124Phase 3Completed
Phase 3, randomised, double-blind trial of setmelanotide in Bardet–Biedl syndrome (BBS), pro-opiomelanocortin deficiency, proprotein convertase subtilisin/kexin type 1 deficiency and 1 more (4 arms), sponsored by Rhythm Pharmaceuticals. Primary endpoints: Maximum Drug Concentration of Setmelanotide After QD Administration in the Run-in Period, Maximum Drug Concentration of Setmelanotide After QW Administration at Week 14 and 5 more. Started Dec 2021; status: completed.
Beyond the preview
Study design, results and competitive context are available in the Gosset platform where reported.
Available in the Gosset platform where reported.
Available in the Gosset platform where reported.
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