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Trials / Completed

CompletedNCT00004578

ABT-378/Ritonavir in Combination With Reverse Transcriptase Inhibitors in Antiretroviral Naïve HIV-Infected Subjects

Phase I/II Study of ABT-378/Ritonavir in Combination With Reverse Transcriptase Inhibitors in Antiretroviral Naive HIV-Infected Patients

Status
Completed
Phase
Phase 1 / Phase 2
Study type
Interventional
Enrollment
100 (actual)
Sponsor
Abbott · Industry
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

To assess the safety, tolerability and antiviral activity of lopinavir/ritonavir when administered orally in antiretroviral-HIV-1 infected subjects.

Conditions

Interventions

TypeNameDescription
DRUGLopinavir/RitonavirLopinavir, range from 200 mg to 400 mg, every 12 hrs and Ritonavir, range from 100 mg to 200 mg, every 12 hrs
DRUGLamivudine150 mg, every 12 hours
DRUGStavudine40 mg every 12 hours

Timeline

Start date
1997-11-01
Primary completion
2005-04-01
Completion
2005-04-01
First posted
2001-08-31
Last updated
2008-04-03

Locations

10 sites across 1 country: United States

Source: ClinicalTrials.gov record NCT00004578. Inclusion in this directory is not an endorsement.

ABT-378/Ritonavir in Combination With Reverse Transcriptase Inhibitors in Antiretroviral Naïve HIV-Infected Subjects (NCT00004578) · Clinical Trials Directory