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Clinical trial

Effect of Intravaginal Prasterone (DHEA) on Moderate to Severe Symptoms of Vulvovaginal Atrophy Due to Menopause, in Women Under Treatment With an Aromatase Inhibitor for Breast Cancer - (Placebo-Controlled, Double Blind and Randomized Phase III Study)

NCT03740945 is registered in ClinicalTrials.gov with EndoCeutics Inc. as lead sponsor.

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Registry record

As filed in ClinicalTrials.gov.

Title
Effect of Intravaginal Prasterone (DHEA) on Moderate to Severe Symptoms of Vulvovaginal Atrophy Due to Menopause, in Women Under Treatment With an Aromatase Inhibitor for Breast Cancer - (Placebo-Controlled, Double Blind and Randomized Phase III Study)
Lead sponsor
EndoCeutics Inc.
Phase
Phase 3
Overall status
Withdrawn
Start date
November 6, 2018
Completion date
December 5, 2019
Enrollment
0 (actual)
Sites
Not reported

Conditions

As the registry lists them; a condition with its own page is linked.

vaginal atrophy in breast cancer patients