Study design & results
Available in the Gosset platform where reported.
Trial intelligence / Profile preview
jRCT2080224996Phase 1Completed
Phase 1, randomised, double-blind trial of danavorexton in hypersomnolence disorder (2 arms), sponsored by Takeda. Primary endpoint: Safety and tolerability of single 9-hour IV infusion of TAK-925 112 mg. Started Dec 2019; 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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