Last reviewed · How we verify
A Multicenter, Randomized, Open Label, Clinical Trial Comparing a QD Regimen of Didanosine, Lamivudine and Efavirenz With a Standard BID Regimen of Zidovudine, Lamivudine and Efavirenz in the Starting Treatment of Human Immunodeficiency Virus Infection (GESIDA 39/03)
The purpose of this study is to compare the antiviral activity of two treatment groups for HIV chronic infection: a QD regimen of didanosine, lamivudine and efavirenz versus a BID regimen of zidovudine, lamivudine and efavirenz. Both will be administered with food in the starting treatment of human immunodeficiency virus infection at Week 48.
Details
| Lead sponsor | Clinical Trial Agency of HIV Study Group |
|---|---|
| Phase | Phase 4 |
| Status | COMPLETED |
| Enrolment | 360 |
| Start date | 2004-06 |
| Completion | 2006-11 |
Conditions
- HIV Infections
Interventions
- didanosine + lamivudine + efavirenz
Primary outcomes
- Percentage of patients with HIV-RNA levels < 50 c/ml (intent-to-treat [ITT])
Countries
Spain