Study of the Effect of Serelaxin on High-sensitivity Cardiac Troponin I (Hs-cTnI) Release in Patients With Chronic Heart Failure

PHASE2TerminatedINTERVENTIONAL
Enrollment

26

Participants

Timeline

Start Date

February 5, 2016

Primary Completion Date

January 11, 2017

Study Completion Date

January 11, 2017

Conditions
Chronic Heart Failure
Interventions
DRUG

Serelaxin

Serelaxin will be administered as a continuous i.v. infusion according to a weight-range adjusted dosing regimen

DRUG

Placebo

Matching placebo i.v infusion

Trial Locations (9)

4031

Novartis Investigative Site, Basel

10117

Novartis Investigative Site, Berlin

17475

Novartis Investigative Site, Greifswald

80636

Novartis Investigative Site, München

81675

Novartis Investigative Site, München

01307

Novartis Investigative Site, Dresden

HU16 5JQ

Novartis Investigative Site, Hull

SW 6NP

Novartis Investigative Site, London

NE2 4HH

Novartis Investigative Site, Tyne and Wear

Sponsors
All Listed Sponsors
lead

Novartis Pharmaceuticals

INDUSTRY