TOL-463 Phase 2 Study for Vaginitis

Status Completed

Clinical Trial Summary

This is a Phase II study designed to assess the safety and efficacy of an investigational product, TOL-463, to treat vaginitis.

Clinical Trial Description

This is a Phase II randomized single blind safety and efficacy study of TOL-463, administered to female adults to treat vaginitis. Participants will be randomly assigned (1:1) to dose TOL-463 Gel or TOL-463 Insert. Study medication will be administered vaginally, once nightly for seven days. The duration of the study for each participant will be approximately 21-30 days. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details

NCT number	NCT02866227
Study type	Interventional
Source	Toltec Pharmaceuticals, LLC
Contact
Status	Completed
Phase	Phase 2
Start date	July 15, 2016
Completion date	June 10, 2017

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