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The primary objective of this study is to compare the efficacy of WC3011 with placebo vaginal gel in postmenopausal women for the relief of vaginal dryness caused by vaginal atrophy as measured by sel...
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Lead Sponsor
Warner Chilcott
NCT06900374 · Vaginal Dryness, Breast Cancer, and more
NCT07250490 · Vulvovaginal Atrophy, Genital Disorder, and more
NCT06846216 · Vulvovaginal Atrophy, Urinary Incontinence, and more
NCT05586711 · Vulvovaginal Atrophy, Genitourinary Syndrome of Menopause
NCT02460302 · Atrophic Vaginitis, Menopause, and more
Warner Chilcott Investigational Study Site
Huntsville, Alabama
Warner Chilcott Investigational Study Site
Mobile, Alabama
Warner Chilcott Investigational Study Site
Phoenix, Arizona
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This clinical trial information is sourced from ClinicalTrials.gov, a service of the U.S. National Institutes of Health.
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