HIGHLIGHTS
- who: Obstetrics Gynecology and collaborators from the staff with the appropriate investigational product lot number for dispensingSubject randomization numbers were available upon entry of subject eligibility information into IWRS. Study treatments were provided in pre-filled, single-use applicators that were sealed in a foil overwrap. A single dose of study drug was administered intravaginally by the clinician on Day , and subjects were double-blinded to receive either AVG, or , grams, or placebo , grams, and remained blinded for the duration of the study. All subjects were instructed to lay flat for at least , minutes following administration of . . .
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