drugset / Trial / NCT00441298

Safety and Effectiveness Study of a Candidate Vaginal Microbicide for Prevention of HIV

NCT00441298

RandomizedSingle-groupDouble-blindPrevention

Summary

This phase IIb, two-arm, double-blinded, randomised, placebo controlled trial comparing 1% Tenofovir gel with a placebo gel is an expanded safety and effectiveness trial involving 900 young women at risk of sexually transmitted HIV infection. Participants will be provided with a supply of single-use, pre-filled applicators according to their randomisation. While in the study, participants will be asked to apply a first dose of the assigned study gel within 12 hours prior to coitus and insert a second dose as soon as possible within 12 hours after coitus. All participants will receive HIV risk reduction counselling, condoms, and syndromic treatment of sexually transmitted infections, if required.

Timeline

Start
2007-05
Primary completion
2009-12
Completion
2010-03

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject Tenofovir Small molecule 1 % Other