CI

At a glance

ClinicalIndex Comparison Record
Phase 3Completed· 61 enrolled
Drug / intervention
Atazanavir + Ritonavirdrug
Likely dose
Atazanavir + Ritonavir 300mgfrom record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT00337467
NCT00337467Phase 3Completed

Phase IIIb Multicenter, Single Arm, Open-Label Pilot Study to Evaluate the Effectiveness and Safety of Maintenance With Atazanavir/Ritonavir as Single Enhanced Protease Inhibitor Therapy in HIV-Infected Patients Evidencing Virologic Suppression OREY (Only REYataz) Study

Bristol-Myers Squibb·interventional·Posted Jun 16, 2006·Updated Jul 19, 2010

In Brief

A Phase 3 clinical trial evaluating Atazanavir + Ritonavir for Human Immunodeficiency Virus (HIV) Infections. Completed, enrolled 61 participants across 7 sites.

Detailed Summary

The main purpose is to explore whether atazanavir/ritonavir (ATV/RTV) single enhanced protease inhibitor therapy can maintain virologic suppression without a marked increase in virologic failure.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
CountriesSpain
Collaborators--

Timeline

Phase 3CompletedFinished
2006200720082009201020112012201320142015201620172018201920202021202220232024202520262027
First PostedJun 16, 2006
Enrollment StartJun 1, 2006
Primary CompletionMay 1, 2008
Study CompletionMay 1, 2009
TodayJul 2, 2026
Enrollment to primary: 1.9 yearsPosted 20.0 years ago

Interventions

Atazanavir + Ritonavirdrug

Capsules, Oral, ATV 300mg + RTV 100mg, once daily, 96 weeks