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Clinical Trial Summary

Objectives of the study:

1. To verify the safety and the efficacy of the study treatment, defined as the persistent control of the virus' replication at 48 weeks after the simplification to maraviroc + darunavir with ritonavir in patients with R5 tropism by viral DNA genotyping.

2. To collect relevant information about the safety, the immunologic and the economic impact of this strategy.


Clinical Trial Description

n/a


Study Design

Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Treatment


Related Conditions & MeSH terms


NCT number NCT01367210
Study type Interventional
Source Catholic University of the Sacred Heart
Contact
Status Terminated
Phase Phase 4
Start date June 2011
Completion date June 2015

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