Study design & results
Available in the Gosset platform where reported.
Trial intelligence / Profile preview
2007-001389-34Phase 2Completed
Phase 2, randomised, double-blind trial of PSD508 and Mefenamic acid in primary dysmenorrhea (PD) (2 arms), sponsored by Plethora Solutions. Primary endpoint: Summed Pain Intensity Difference over 8 hours after first treatment. Started Oct 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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