Clinical trial

Efficacy and Safety of Tenofovir DF/Atazanavir Enhanced With Low Dose of…

NCT00122577 · French National Agency for Research on AIDS and Viral Hepatitis, Other · Terminated

Key facts

NCT number NCT00122577
Title Efficacy and Safety of Tenofovir DF/Atazanavir Enhanced With Low Dose of Ritonavir in HIV-Infected Patients
Official title Randomized Open Label Study Assessing the Antiviral Activity, Toxicity and Pharmacologic Interaction of Tenofovir DF/Atazanavir Enhanced With Low Dose of Ritonavir as Part of a Salvage Regimen in HIV Infected Patients With Multiple Treatment Failures (ANRS 107 Trial PUZZLE 2)
Lead sponsor French National Agency for Research on AIDS and Viral Hepatitis, Other
Collaborators Bristol-Myers Squibb Industry Gilead Sciences
Status Terminated
Phase Phase 2
Study type Interventional
Conditions HIV Infections
Intervention type Drug
Interventions Tenofovir, Atazanavir, Ritonavir
Enrollment 50
Start date Mar 1, 2002
Completion Jul 1, 2004
First posted Jul 22, 2005
Last update posted Jul 28, 2005
Countries France

At a glance

  • 1–9 Study sites
  • No 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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