drugset / Trial / NCT00288730

A Study of Two Doses of Intravenous NATRECOR hBNP (Nesiritide) in Patients With Worsening Congestive Heart Failure Who Have Difficulty Breathing at Rest

NCT00288730

Phase 3 Completed 127 enrolled Scios, Inc.
RandomizedParallel-groupDouble-blindTreatment

Summary

The purpose of this study is to assess the safety and efficacy of two doses of intravenous NATRECOR® hBNP (a recombinant form of the natural human peptide normally secreted by the heart) versus placebo in the treatment of patients with symptomatic, decompressed congestive heart failure (CHF).

Timeline

Start
1996-10
Primary completion
Completion
1997-08

Drugs

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