Clinical trial

Comparison of Two Dosing Regimens of GW433908/Ritonavir Versus…

NCT00025727 · GlaxoSmithKline, Industry · Unknown status

Key facts

NCT number NCT00025727
Title Comparison of Two Dosing Regimens of GW433908/Ritonavir Versus Lopinavir/Ritonavir for 48 Weeks in HIV Patients Who Have Taken Protease Inhibitors and Experienced Virological Failure
Official title A Phase III, Randomized, Multicenter, Parallel Group, Open-Label, Three Arm Study to Compare the Efficacy and Safety of Two Dosing Regimens of GW433908/Ritonavir (700mg/100mg Twice Daily or 1400mg/200mg Once Daily) Versus Lopinavir/Ritonavir (400mg/100mg Twice Daily) for 48 Weeks in Protease…
Lead sponsor GlaxoSmithKline, Industry
Status Unknown status
Phase Phase 3
Study type Interventional
Conditions HIV Infections
Intervention type Drug
Interventions Lopinavir/Ritonavir, Ritonavir, GW433908
Enrollment 330
Start date May 1, 2001
First posted Oct 16, 2001
Last update posted Jun 24, 2005
Countries United States

At a glance

  • 10–99 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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