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Clinical trial

A Phase 3, Randomized, Double-Blind Study to Evaluate the Safety and Efficacy of Switching From a Regimen of Dolutegravir and Either Emtricitabine/Tenofovir Alafenamide or Emtricitabine/Tenofovir Disoproxil Fumarate to a Fixed Dose Combination of Bictegravir/ Emtricitabine/Tenofovir Alafenamide in HIV-1 Infected Subjects Who Are Virologically Suppressed

NCT03110380 is registered in ClinicalTrials.gov with Gilead Sciences as lead sponsor.

NCT NCT03110380
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Registry record

As filed in ClinicalTrials.gov.

Title
A Phase 3, Randomized, Double-Blind Study to Evaluate the Safety and Efficacy of Switching From a Regimen of Dolutegravir and Either Emtricitabine/Tenofovir Alafenamide or Emtricitabine/Tenofovir Disoproxil Fumarate to a Fixed Dose Combination of Bictegravir/ Emtricitabine/Tenofovir Alafenamide in HIV-1 Infected Subjects Who Are Virologically Suppressed
Lead sponsor
Gilead Sciences
Phase
Phase 3
Overall status
Completed
Start date
June 12, 2017
Completion date
February 10, 2021
Enrollment
567 (actual)
Sites
94

Conditions

As the registry lists them; a condition with its own page is linked.

hiv-1-infection