Vocabria 400 mg prolonged-release suspension for injection
Sponsors
Viiv Healthcare UK Limited, Stichting Radboud universitair medisch centrum, Gilead Sciences Inc.
Conditions
HIV-1HIV-1 infectionHIV-infected
Phase 3
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 participant-determined optional switch to long-acting intramuscular cabotegravir plus rilpivirine every two months for the maintenance of virologic suppression in antiretroviral therapy naive adults living with HIV-1.
Active, not recruitingCTIS2023-503893-19-00
Start: 2023-12-06Target: 67Updated: 2025-12-29
A Phase 3, Randomized, Open-label Study to Evaluate the Efficacy and Safety of Switching to Long-acting Antiretroviral Therapy of Broadly Neutralizing Antibodies Teropavimab and Zinlirvimab in Combination With the Capsid Inhibitor Lenacapavir Twice-Yearly Versus Cabotegravir and Rilpivirine Every 8 Weeks in Virologically Suppressed Adults With HIV-1 on Oral Daily Antiretroviral Therapy
Not yet recruitingCTIS2025-524335-39-00
Target: 37Updated: 2026-07-22