Clinical trial

Study to Evaluate the Efficacy, Safety, and Tolerability of Long-acting…

NCT02938520 · ViiV Healthcare, Industry · Active, not recruiting

Key facts

NCT number NCT02938520
Title Study to Evaluate the Efficacy, Safety, and Tolerability of Long-acting Intramuscular Cabotegravir and Rilpivirine for Maintenance of Virologic Suppression Following Switch From an Integrase Inhibitor in HIV-1 Infected Therapy Naive Participants
Official title A Phase III, Randomized, Multicenter, Parallel-group, Open-Label Study Evaluating the Efficacy, Safety, and Tolerability of Long-Acting Intramuscular Cabotegravir and Rilpivirine for Maintenance of Virologic Suppression Following Switch From an Integrase Inhibitor Single Tablet Regimen in HIV-1…
Lead sponsor ViiV Healthcare, Industry
Collaborators Janssen Pharmaceuticals Industry GlaxoSmithKline
Status Active, not recruiting
Phase Phase 3
Study type Interventional
Conditions HIV Infections
Intervention type Drug
Interventions Cabotegravir (CAB) tablet, Rilpivirine (RPV) tablet, Cabotegravir - Injectable Suspension (CAB LA), Rilpivirine - Injectable Suspension (RPV LA), ABC/DTG/3TC STR - Tablet, DTG Tablet
Enrollment 631
Start date Oct 27, 2016
Primary completion Aug 30, 2018
Completion Dec 31, 2025
First posted Oct 19, 2016
Last update posted Dec 31, 2025
Countries Canada, France, Germany, Italy, Japan, Netherlands, Russia, South Africa, Spain, United Kingdom, United States

At a glance

  • 100–999 Study sites
  • Yes Results posted
  • None Linked FDA submissions

Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.

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