DARE-BV1 in the Treatment of Bacterial Vaginosis (DARE-BVFREE)

Status Completed

Clinical Trial Summary

This is a multicenter, randomized, double-blind, placebo-controlled study of DARE-BV1 (clindamycin phosphate vaginal gel, 2%) (QD x 1 day) compared to placebo vaginal gel (HEC Universal Placebo Gel) (QD × 1 day) for the treatment of bacterial vaginosis. Patients will be evaluated at three time points: a Day 1 Screening/Randomization visit, a Day 7-14 Interim Assessment visit, and a Day 21 - 30 Test of Cure [TOC] visit). Patients who discontinue prematurely from the study will receive a safety follow-up phone call between Day 21-30. The total study duration will be approximately one month for each individual patient.

Clinical Trial Description

n/a

Study Design

Related Conditions & MeSH terms

Clinical Trial Details

NCT number	NCT04370548
Study type	Interventional
Source	Daré Bioscience, Inc.
Contact
Status	Completed
Phase	Phase 3
Start date	June 16, 2020
Completion date	December 7, 2020

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