Clinical trial

Safety and Efficacy of Veronate® Versus Placebo in Preventing Nosocomial…

NCT00113191 · Bristol-Myers Squibb, Industry · Completed

Key facts

NCT number NCT00113191
Title Safety and Efficacy of Veronate® Versus Placebo in Preventing Nosocomial Staphylococcal Sepsis in Premature Infants
Official title A Phase III, Randomized, Double-blind, Multi-center Clinical Trial Comparing the Safety and Efficacy of Veronate® Versus Placebo for the Prevention of Nosocomial Staphylococcal Sepsis in Premature Infants (Birth Weight 500 - 1250 g)
Lead sponsor Bristol-Myers Squibb, Industry
Status Completed
Study type Interventional
Conditions Nosocomial Infections, Sepsis, Staphylococcal Infections, Candidemia
Intervention type Drug
Interventions Veronate
Enrollment 2,000
Start date May 1, 2004
Primary completion Jun 1, 2006
Completion Jun 1, 2006
First posted Jun 7, 2005
Last update posted Aug 2, 2012
Countries Canada, United States

At a glance

  • 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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