Study design & results
Available in the Gosset platform where reported.
Trial intelligence / Profile preview
NCT00604825Phase 2Completed
Phase 2, randomised, double-blind trial of GSK232802 in vasomotor symptoms (4 arms), sponsored by GSK. Primary endpoints: Number of Participants With Adverse Events (AE) and Serious Adverse Events (SAE) up to 21 weeks, Mean Change in Frequency of Vasomotor Symptoms (VMS) From Baseline at Week 12 and 4 more. Started Jul 2007; 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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