A Phase IIIb, Randomized, Multicenter, Parallel-group, Non-inferiority, Open-label Study Evaluating the Efficacy, Safety, and Tolerability of Long-acting Cabotegravir Plus Long-acting Rilpivirine Administered Every 8 Weeks or Every 4 Weeks in HIV-1-infected Adults who are Virologically Suppressed

Trial Profile

A Phase IIIb, Randomized, Multicenter, Parallel-group, Non-inferiority, Open-label Study Evaluating the Efficacy, Safety, and Tolerability of Long-acting Cabotegravir Plus Long-acting Rilpivirine Administered Every 8 Weeks or Every 4 Weeks in HIV-1-infected Adults who are Virologically Suppressed

Active, no longer recruiting
Phase of Trial: Phase III

Latest Information Update: 05 Aug 2018

At a glance

  • Drugs Cabotegravir (Primary) ; Cabotegravir (Primary) ; Rilpivirine (Primary) ; Rilpivirine (Primary)
  • Indications HIV-1 infections
  • Focus Registrational; Therapeutic Use
  • Acronyms ATLAS-2M
  • Sponsors ViiV Healthcare
  • Most Recent Events

    • 14 Jun 2018 Status changed from recruiting to active, no longer recruiting.
    • 11 Dec 2017 Planned End Date changed from 18 Feb 2022 to 7 Mar 2022.
    • 11 Dec 2017 Planned primary completion date changed from 18 Feb 2022 to 31 May 2019.
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