Study to Evaluate Safety, Tolerability, Pharmacokinetics and Pharmacodynamics of LCZ696 Followed by a 52-week, Double-blind Study of LCZ696 Compared With Enalapril in Pediatric Patients With Heart Failure

Last updated:
2026-07-11
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View trial details

Overview

Official protocol title:

MULTICENTER, OPEN-LABEL, STUDY TO EVALUATE SAFETY, TOLERABILITY, PHARMACOKINETICS AND, PHARMACODYNAMICS OF LCZ696 FOLLOWED BY A 52-WEEK RANDOMIZED, DOUBLE-BLIND, PARALLEL GROUP, ACTIVE-CONTROLLED STUDY TO EVALUATE THE EFFICACY AND SAFETY OF LCZ696 COMPARED WITH ENALAPRIL IN PEDIATRIC PATIENTS FROM1 MONTH TO < 18 YEARS OF AGE WITH HEART FAILURE DUE TO SYSTEMIC LEFT VENTRICLE SYSTOLIC DYSFUNCTION

Intervention/treatment:
LCZ696 (SACUBITRIL-VALSARTAN)
Medical condition:
HEART FAILURE
Protocol code:
CLCZ696B2319
Control number:
200879
Status:
Closed
Approved:
December 28, 2016
Date Completed:
Trial phase:
Phase 2, Phase 3
For more information:
ClinicalTrials.gov - NCT02678312
This is an external link. The information is not authorized by the Government of Canada.

Eligibility

Sex: ALL
Age
1 Month to 17 Years
Accepts healthy volunteers: No

Contacts and locations

Contact
Name
Study Director
Organization
Novartis Pharmaceuticals
Phone:
862-778-8300
Sponsor
NOVARTIS PHARMACEUTICALS CANADA INC

Locations

Alberta

Novartis Investigative Site
Edmonton, Alberta, T6G 1C9

Ontario

Novartis Investigative Site
Toronto, Ontario, M5G 1X8

Results

See the results from the trial NCT02678312. This is an external link. The information is not authorized by the Government of Canada.

Date posted:
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