drugset / Trial / NCT02151383

Pharmacokinetics & Safety of Serelaxin on Top of Standard of Care Therapy in Pediatric Patients With Acute Heart Failure

NCT02151383

Phase 2 Terminated 12 enrolled Novartis Pharmaceuticals
NaSingle-groupOpen-labelTreatment

Summary

The purpose of the study was to evaluate the safety, tolerability and pharmacokinetics of an intravenous infusion of serelaxin on top of standard of care therapy, in pediatric patients with acute heart failure (AHF)

Timeline

Start
2014-09-05
Primary completion
2017-04-03
Completion
2017-04-03

Drugs

EvaluationDrugModalityDoseRoute
Subject Serelaxin Protein / enzyme biologic Intravenous

Indications