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Safety and Acceptability of Tenofovir 1% Gel in Adolescent Females

HIV Prevention Clinical Trial

Official title:
Phase I Safety and Acceptability of Tenofovir 1% Gel in Adolescent Females

Clinical Trial Summary

The purpose of this trial is to assess the safety and acceptability of Tenofovir (TFV) 1% gel in adolescent females over 12 weeks of a minimum of twice weekly dosing following the BAT24 regimen.

Clinical Trial Description

n/a

Study Design

Allocation: Randomized, Endpoint Classification: Safety Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Caregiver, Investigator, Outcomes Assessor), Primary Purpose: Prevention

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT02245945
Study type Interventional
Source CONRAD
Contact
Status Withdrawn
Phase Phase 1
View Details
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