Study design & results
Available in the Gosset platform where reported.
Trial intelligence / Profile preview
NCT06268054Phase 3Not yet recruiting
Phase 3, randomised, double-blind trial in primary dysmenorrhea (PD) comparing DEH113 with Placebo (2 arms). Primary endpoint: Sum of Total Pain Relief over 0-6 hours post-dose. Planned start Feb 2025; status: not yet recruiting.
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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