drugset / Trial / NCT02013141

Telavancin Pediatric PK Study (Ages >12 Months to 17 Years)

NCT02013141

Phase 1 Terminated 22 enrolled Cumberland Pharmaceuticals
NaSingle-groupOpen-labelBasic science

Summary

This is a multicenter, open-label, single-dose pharmacokinetic (PK) study. Infants, children, and adolescents will receive a single 10 mg/kg dose of telavancin infused intravenously (IV) over 60 minutes

Timeline

Start
2014-12
Primary completion
2021-03
Completion
2021-03

Drugs

EvaluationDrugModalityDoseRoute
Subject Telavancin Other / unclassified 10 mg/kg Intravenous