HIV Infections Clinical Trial
Official title:
A Phase 3b, Open-Label, Single Arm Study to Evaluate the Safety and Efficacy of Cobicistat-boosted Darunavir Plus Two Fully Active Nucleoside Reverse Transcriptase Inhibitors in HIV-1 Infected, Antiretroviral Treatment-Naïve and -Experienced Adults With No Darunavir Resistance-associated Mutations
This study is to evaluate the safety and tolerability of cobicistat-boosted darunavir plus
two fully active nucleoside analogue reverse transcriptase inhibitors in HIV 1 infected,
antiretroviral treatment-naive and treatment-experienced adults with no darunavir (DRV)
resistance-associated mutations.
After the Week 48 Visit, participants will be given the option to participate in an
extension period to receive cobicistat and attend visits every 12 weeks until it becomes
commercially available, or until Gilead Sciences elects to terminate development of
cobicistat.
n/a
Endpoint Classification: Safety/Efficacy Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment
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