drugset / Trial / NCT00885482
Atazanavir and Lamivudine for Treatment Simplification
NaSingle-groupOpen-labelTreatment
Summary
Objectives of the study: 1. To verify the safety of the study treatment, defined as the persistent control of the virus' replication at 48 weeks after the simplification to lamivudine + atazanavir with ritonavir. 2. To collect relevant information about the safety and the metabolic impact of this strategy in order to eventually design a non-inferiority randomized controlled trial for the evaluation of the safety and the efficacy of this strategy in the future.
Timeline
- Start
- 2009-05
- Primary completion
- 2010-05
- Completion
- 2011-05
Drugs
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | Atazanavir | Other / unclassified | 300 mg | — |
| Subject | Lamivudine | Other / unclassified | 300 mg | — |
| Background | Ritonavir | Other / unclassified | 100 mg | — |