drugset / Trial / NCT02766023

LACTIN-V Study for Recurrent Bacterial Vaginosis

NCT02766023

RandomizedParallel-groupDouble-blindPrevention

Summary

This Phase 2b trial is designed to provide a screening evaluation for the hypothesis that, following a 5-day treatment with MetroGel® to treat BV, L. crispatus CTV-05 (LACTIN-V, Osel, Inc.) administered at 2 x 10\^9 cfu/dose using a vaginal applicator reduces the 12-week incidence of BV recurrence when compared to placebo. The primary objectives of this study are: 1) To estimate the efficacy of repeated doses of LACTIN-V (2 x 10\^9 cfu/dose) as compared to placebo in preventing BV recurrence by 12 weeks following treatment of BV with MetroGel vaginal gel (MetroGel). 2) To assess the safety of LACTIN-V over 24 weeks by comparing the incidence of AEs between individuals randomized to LACTIN-V or placebo.

Timeline

Start
2016-06-03
Primary completion
2019-02-11
Completion
2019-02-11

Drugs

EvaluationDrugModalityDoseRoute
Subject LACTIN-V Other / unclassified 2e+09 unknown Other
Background Metronidazole Small molecule 7.5 unknown Other

Indications