Open-label, Multiple-dose, Phase III Study of the Population Pharmacokinetics of I.V. Synercid in 75 Pediatric Patients
Status:
Terminated
Trial end date:
2005-01-01
Target enrollment:
Participant gender:
Summary
Open-label, multicenter, multiple-dose, study of population pharmacokinetics of I.V. Synercid
(7.5 mg/kg every 8 hours) in 75 pediatric patients. The purpose is to assess the population
pharmacokinetics of Synercid in pediatric patients and to collect additional safety and
efficacy data in pediatric patients.