Clinical trial
A Phase III, 48-Week, Open-Label, Randomized, Multicenter Study of the Safety and Efficacy of the Abacavir/Lamivudine Fixed-Dose Combination Tablet Administered QD Versus Abacavir + Lamivudine Administered BID in Combination With a PI or NNRTI in Antiretroviral Experienced Patients.
NCT00046176 is registered in ClinicalTrials.gov with ViiV Healthcare as lead sponsor.
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Registry record
As filed in ClinicalTrials.gov.
- Title
- A Phase III, 48-Week, Open-Label, Randomized, Multicenter Study of the Safety and Efficacy of the Abacavir/Lamivudine Fixed-Dose Combination Tablet Administered QD Versus Abacavir + Lamivudine Administered BID in Combination With a PI or NNRTI in Antiretroviral Experienced Patients.
- Lead sponsor
- ViiV Healthcare
- Phase
- Phase 3
- Overall status
- Completed
- Start date
- August 26, 2002
- Completion date
- May 17, 2004
- Enrollment
- 240
- Sites
- 56
Conditions
As the registry lists them; a condition with its own page is linked.
hiv infection, infection, human immunodeficiency virus i