Trial intelligence / Profile preview

MTN-038: 90-Day Tenofovir Intravaginal Ring PK and Safety

NCT03670355Phase 1Completed

Sponsor
National Institute of Allergy and Infectious Diseases
Start
Jan 2019
Primary completion
Sep 2019
Modality
Small Molecules
Countries
1
01

Overview

Phase 1, randomised, double-blind trial in human immunodeficiency virus infection (HIV) comparing Tenofovir (TFV) Intravaginal Ring (IVR) with Placebo IVR (2 arms). Primary endpoints: Tenofovir Levels in Plasma at Day 92, Tenofovir Levels in Cervicovaginal Fluid at Day 92 and 5 more. Started Jan 2019; status: completed.

02

Drugs

tenofovir
03

Conditions

human immunodeficiency virus infection (HIV)

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