Published in Pharma Law Weekly, December 16th, 2008
"Primary efficacy endpoints included change from baseline to week 12 in vaginal cytology, vaginal pH, and most bothersome urogenital symptoms score. Grading of vaginal health was a secondary efficacy assessment. Safety assessments included endometrial biopsy, physical and gynecologic examinations, and recording adverse...
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Source: Pharma Law Weekly (2008-12-16)
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