Study design & results
Available in the Gosset platform where reported.
Trial intelligence / Profile preview
NCT04234204Phase 3Completed
Phase 3, randomised, double-blind trial in vasomotor symptoms comparing Fezolinetant group with Placebo group (2 arms). Primary endpoints: Mean change from baseline in the frequency of moderate to severe vasomotor symptoms (VMS) at 4 weeks and Mean change from baseline in the severity of moderate to severe vasomotor symptoms (VMS) at 4 weeks. Started Mar 2020; 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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