Overview
A Study of Raltegravir in a Diverse Cohort of HIV-Infected Patients (0518-055)
Status:
Completed
Completed
Trial end date:
2011-02-01
2011-02-01
Target enrollment:
0
0
Participant gender:
All
All
Summary
A study to test the safety and effect of twice daily raltegravir in a diverse cohort of patients currently infected with human immunodeficiency virus (HIV), where at least 50% are African American and at least 25% are female, either having received antiretroviral drugs before or not.Phase:
Phase 3Accepts Healthy Volunteers?
NoDetails
Lead Sponsor:
Merck Sharp & Dohme Corp.Treatments:
Raltegravir Potassium
Criteria
Inclusion Criteria:- Patient is HIV positive
- Patient agrees to use (or have their partner use) birth control as defined by the
study doctor
Exclusion Criteria:
- If female, pregnant or breastfeeding
- Patient has used an investigational agent in the last 30 days
- Patient has acute hepatitis
- Patient has received MK0518 (raltegravir) before
- Patient has used another experimental HIV-integrase inhibitor