drugset / Trial / NCT00271557

A Study to Develop Additional Safety and Clinical Experience With NATRECOR hBNP (Nesiritide) in the Treatment of Patients With Worsening Congestive Heart Failure Who Require Inpatient Intravenous Therapy With Medications That Influence the Tone and Caliber of Blood Vessels

NCT00271557

Phase 3 Completed 305 enrolled Scios, Inc.
RandomizedParallel-groupOpen-labelTreatment

Summary

The purpose of this safety study is to evaluate NATRECOR® hBNP (a recombinant form of the natural human peptide normally secreted by the heart in response to heart failure), in subjects with worsening congestive heart failure for whom inpatient intravenous therapy with medications that influence the tone and caliber of blood vessels is deemed appropriate.

Timeline

Start
1997-01
Primary completion
Completion
1997-12

Drugs

EvaluationDrugModalityDoseRoute
Subject Nesiritide Protein / enzyme biologic 0.015 ug/kg Intravenous
Subject Nesiritide Protein / enzyme biologic 0.03 ug/kg Intravenous