Trials / Completed
CompletedNCT00002217
A Study of Combivir Plus Abacavir Plus 141W94 in Patients Who Previously Have Used Anti-HIV Drugs
Combivir, 1592U89, 141W94 Triple Antiretroviral, Experienced Patient Trial
- Status
- Completed
- Phase
- N/A
- Study type
- Interventional
- Enrollment
- —
- Sponsor
- Glaxo Wellcome · Industry
- Sex
- All
- Age
- 18 Years
- Healthy volunteers
- Not accepted
Summary
The purpose of this study is to test the effectiveness of Combivir plus abacavir plus 141W94 in patients who previously have used anti-HIV drugs.
Detailed description
In this open-label study antiretroviral-experienced patients receive Combivir (3TC/AZT tablet) plus 1592U89 (abacavir) and 141W94 twice daily for 48 weeks.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | Lamivudine/Zidovudine | |
| DRUG | Abacavir sulfate | |
| DRUG | Amprenavir |
Timeline
- First posted
- 2001-08-31
- Last updated
- 2005-06-24
Locations
1 site across 1 country: United States
Source: ClinicalTrials.gov record NCT00002217. Inclusion in this directory is not an endorsement.