MedPath

A Study of Retrovir and Epivir Alone or in Combination With 141W94 in HIV-Infected Patients

Phase 3
Completed
Conditions
HIV Infections
Registration Number
NCT00002195
Lead Sponsor
Glaxo Wellcome
Brief Summary

The purpose of this study is to see if it is safe and effective to add 141W94 to an anti-HIV regimen that includes retrovir plus epivir.

Detailed Description

This is a double-blind, placebo-controlled, two-arm study comparing treatment with a triple regimen consisting of 141W94, retrovir, and epivir and a double regimen consisting of retrovir and epivir.

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
290
Inclusion Criteria

Not provided

Exclusion Criteria

Not provided

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Primary Outcome Measures
NameTimeMethod
Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (9)

Chicago Ctr for Clinical Research

🇺🇸

Chicago, Illinois, United States

Dr Bruce Rashbaum

🇺🇸

Washington, District of Columbia, United States

Community Research Initiative of South Florida

🇺🇸

Coral Gables, Florida, United States

Community Research Initiative of Central Florida

🇺🇸

Maitland, Florida, United States

Saint Vincent's AIDS Ctr

🇺🇸

New York, New York, United States

Pacific Oaks Research

🇺🇸

Beverly Hills, California, United States

Univ of Miami School of Medicine

🇺🇸

Miami, Florida, United States

Methodist Hosp

🇺🇸

Memphis, Tennessee, United States

Community Research Initiative of New England

🇺🇸

Brookline, Massachusetts, United States

© Copyright 2025. All Rights Reserved by MedPath