Clinical trial

Evaluation of Efficacy and Safety of Peramivir in Adults With Acute Serious or…

NCT00453999 · BioCryst Pharmaceuticals, Industry · Completed

Key facts

NCT number NCT00453999
Title Evaluation of Efficacy and Safety of Peramivir in Adults With Acute Serious or Potentially Life-threatening Influenza
Official title Phase II, Multicenter, Randomized, Double-Mask, Double-Dummy Study Comparing Efficacy and Safety of Intravenous Peramivir Once Daily Versus Oral Oseltamivir Twice Daily in Adults With Acute Serious or Potentially Life-Threatening Influenza
Lead sponsor BioCryst Pharmaceuticals, Industry
Status Completed
Phase Phase 2
Study type Interventional
Conditions Influenza
Intervention type Drug
Interventions Peramivir 200 mg, Peramivir 400 mg, Oseltamivir
Enrollment 137
Start date Jul 1, 2007
Primary completion Sep 1, 2008
Completion Aug 1, 2009
First posted Mar 29, 2007
Last update posted Feb 12, 2015
Countries Australia, Canada, Hong Kong, New Zealand, Singapore, South Africa, United States

At a glance

  • 10–99 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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