A PHASE IIIB, MULTI-CENTER, NON-RANDOMIZED, PARALLEL-GROUP, OPEN-LABEL, HYBRID
TYPE I STUDY EVALUATING THE EFFICACY, SAFETY, IMPLEMENTATION EFFECTIVENESS, AND
PATIENT-REPORTED OUTCOMES OF ORAL DOLUTEGRAVIR/LAMIVUDINE ONCE-DAILY AS A FIRST-LINE
REGIMEN FOLLOWED BY PARTICIPANTS-DETERMINED OPTIONAL SWITCH TO LONG-ACTING
INTRAMUSCULAR CABOTEGRAVIR PLUS RILPIVIRINE EVERY TWO MONTHS FOR THE MAINTENANCE
OF VIROLOGIC SUPPRESSION IN ANTIRETROVIRAL THERAPY NAÏVE ADULTS LIVING WITH HIV-1
- Registry ID
- 219700 (VOLITION)
- Source registry
- HEALTH_CANADA
- Status
- Ongoing
- Phase
- PHASE3
- Study type
- INTERVENTIONAL
- Sponsor
- VIIV HEALTHCARE UK LIMITED
- Start date
- 2024-02-23
- Last update
- 2023-07-20
Conditions
- HUMAN IMMUNODEFICIENCY VIRUS (HIV)
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