drugset / Trial / NCT00752037

Safety Study of Lopinavir/Ritonavir With Raltegravir in HIV-infected Patients

NCT00752037

Phase 4 Completed 30 enrolled Saint Michael's Medical Center Abbott · collab
Non-randomizedSingle-groupOpen-labelTreatment

Summary

A single center, open label, 48-week study of lopinavir/ritonavir in combination with raltegravir. 30 patients, both naïve and experienced, will be enrolled. 15 treatment naïve patients and 15 treatment experienced patients enrolled

Timeline

Start
2008-09
Primary completion
2010-04
Completion
2010-06

Drugs

EvaluationDrugModalityDoseRoute
Subject Raltegravir Other / unclassified 400 mg Oral
Subject lopinavir/ritonavir Unknown 100 mg Oral
Subject lopinavir/ritonavir Unknown 400 mg Oral