Study design & results
Available in the Gosset platform where reported.
Trial intelligence / Profile preview
NCT01256671Phase 3Completed
Phase 3, open-label, single-arm trial of prasterone in vaginal atrophy, sponsored by Endoceutics. Primary endpoints: Long-term Safety of Intravaginal Prasterone (DHEA): Endometrium at 52 weeks and Long-term Safety of Intravaginal Prasterone (DHEA): Serum Steroid Levels at 52 weeks. Started Dec 2010; 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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