Clinical trial

Study of Lopinavir/Ritonavir Tablets Comparing Once-Daily Versus Twice-Daily…

NCT00358917 · Abbott, Industry · Completed

Key facts

NCT number NCT00358917
Title Study of Lopinavir/Ritonavir Tablets Comparing Once-Daily Versus Twice-Daily Administration When Coadministered With Nucleoside/Nucleotide Reverse Transcriptase Inhibitors in Antiretroviral-Experienced Human Immunodeficiency Virus Type 1 Infected Subjects
Official title A Phase 3, Randomized, Open-Label Study of Lopinavir/Ritonavir (LPV/r) Tablets 800/200 Milligram (mg) Once-Daily (QD) Versus 400/100 mg Twice-Daily (BID) When Coadministered With Nucleoside/Nucleotide Reverse Transcriptase Inhibitors (NRTIs) in Antiretroviral-Experienced, Human Immunodeficiency…
Lead sponsor Abbott, Industry
Status Completed
Phase Phase 3
Study type Interventional
Conditions Human Immunodeficiency Virus Infections
Intervention type Drug
Interventions lopinavir/ritonavir (LPV/r) tablet with nucleoside/nucleotide reverse transcriptase inhibitors (NRTIs)
Enrollment 599
Start date Aug 1, 2006
Primary completion Nov 1, 2008
Completion Nov 1, 2008
First posted Aug 1, 2006
Last update posted Apr 11, 2011
Countries United States

At a glance

  • 1–9 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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