Study design & results
Available in the Gosset platform where reported.
Trial intelligence / Profile preview
NCT02023606Phase 1Completed
Phase 1, open-label, single-arm trial of molindone in intermittent explosive disorder (IED), sponsored by Supernus Pharmaceuticals, Inc. Primary endpoint: Urinary and fecal recoveries of total radioactivity at 10 days. Started Nov 2013; 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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