Clinical Trials Directory

Trials / Completed

CompletedNCT00038220

Effectiveness of ABT-378/Ritonavir Plus Lamivudine Plus Efavirenz Plus Tenofovir DF in HIV-Infected Patients

A Phase I/II, Open Label Study to Evaluate the Ability of Combination Therapy With ABT-378/Ritonavir (Kaletra), Lamivudine (Epivir), Efavirenz (Sustiva)and Tenofovir DF to Completely Suppress Viral Replication in Subjects Infected With HIV-1

Status
Completed
Phase
Phase 2
Study type
Interventional
Enrollment
40 (planned)
Sponsor
Abbott · Industry
Sex
All
Age
18 Years – 65 Years
Healthy volunteers
Not accepted

Summary

The purpose of this study is to see if a novel 4-drug anti-HIV combination can suppress the growth of HIV in patients infected with the virus.

Conditions

Interventions

TypeNameDescription
DRUGLopinavir/ritonavir
DRUGEfavirenz
DRUGLamivudine
DRUGTenofovir DF

Timeline

Start date
2000-07-01
First posted
2002-05-30
Last updated
2006-07-27

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT00038220. Inclusion in this directory is not an endorsement.

Effectiveness of ABT-378/Ritonavir Plus Lamivudine Plus Efavirenz Plus Tenofovir DF in HIV-Infected Patients (NCT00038220) · Clinical Trials Directory