Overview

A Study in Underrepresented Patient Population or Regimen Tolerability: SUPPoRT

Status:
Completed
Trial end date:
2011-07-01
Target enrollment:
Participant gender:
Summary
The hope of this study is to gather data and information about the tolerability and effectiveness of Lexiva versus Sustiva in patients who have have been generally underrepresented in clinical trials.
Phase:
Phase 3
Details
Lead Sponsor:
Georgetown University
Collaborator:
GlaxoSmithKline
Treatments:
Abacavir
Efavirenz
Fosamprenavir
Lamivudine