Study design & results
Available in the Gosset platform where reported.
Trial intelligence / Profile preview
2025-521460-36-00Phase 4Authorised
Phase 4, randomised trial of estradiol, progesterone, estradiol valerate, estriol and promestriene in Cervical Cancer (CC), female sexual dysfunction (FSD) and vaginal atrophy (2 arms), sponsored by IDIBAPS. Primary endpoint: Global FSFI score at 12 months after treatment. Planned start May 2025; status: authorised.
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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