RPV
Sponsors
ViiV Healthcare
Conditions
HIV InfectionsInfection, Human Immunodeficiency Virus
Phase 1
Bioequivalence Study of a Fixed-dose Combination (FDC) of Dolutegravir (DTG) and Rilpivirine (RPV)
CompletedNCT02741557
Start: 2016-05-11End: 2016-10-24Updated: 2019-07-15
A Study to Investigate Pharmacokinetics, Safety and Tolerability of Long-Acting Cabotegravir Plus Recombinant Human Hyaluronidase PH20 in Healthy Adult Participants
RecruitingNCT05418868
Start: 2022-06-14End: 2027-06-08Target: 214Updated: 2025-12-18
Phase 2
A Phase IIb Study to Evaluate a Long-Acting Intramuscular Regimen for Maintenance of Virologic Suppression (Following Induction With an Oral Regimen of GSK1265744 and Abacavir/Lamivudine) in Human Immunodeficiency Virus Type 1 (HIV-1) Infected, Antiretroviral Therapy-Naive Adult Subjects
CompletedNCT02120352
Start: 2014-04-28End: 2023-04-20Updated: 2024-06-12
Phase 2b, Open-label, Multicenter, Rollover Study to Assess Antiviral Activity and Safety of Long-acting (LA) Cabotegravir (CAB) Plus LA Rilpivirine (RPV), Administered Every 2 Months (Q2M), in Human Immunodeficiency Virus (HIV)-Positive Participants From the LATTE Study
CompletedNCT03639311
Start: 2018-09-24End: 2023-01-30Updated: 2024-06-11