Trial Assessing Efficacy, Safety and Tolerability of Proprotein Convertase Subtilisin/Kexin Type 9 (PCSK9) Inhibition in Paediatric Subjects With Genetic Low-Density Lipoprotein (LDL) Disorders

Last updated:
2026-07-11
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View trial details

Overview

Official protocol title:

DOUBLE-BLIND, RANDOMIZED, MULTICENTER, PLACEBO-CONTROLLED, PARALLEL GROUP STUDY TO CHARACTERIZE THE EFFICACY, SAFETY AND TOLERABLITY OF 24 WEEKS OF EVOLOCUMAB FOR LOW DENSITY LIPOPROTEIN-CHOLESTEROL (LSL-C) REDUCTION, AS ADD-ON TO DIET AND LIPID-LOWERING THERAPY, IN PEDIATRIC SUBJECTS 10 TO 17 YEARS OF AGE WITH HETEROZYGOUS FAMILIAL HYPERCHOLESTEROLEMIA (HEFH)

Intervention/treatment:
AMG 145 (EVOLOCUMAB)
Medical condition:
HETEROZYGOUS FAMILIAL HYPERCHOLESTEROLEMIA
Protocol code:
20120123
Control number:
182247
Status:
Closed
Approved:
March 19, 2015
Date Completed:
Trial phase:
Phase 3
For more information:
ClinicalTrials.gov - NCT02392559
This is an external link. The information is not authorized by the Government of Canada.

Eligibility

Sex: ALL
Age
10 Years to 17 Years
Accepts healthy volunteers: No

Contacts and locations

Contact
Name
Study Director
Organization
Amgen Inc.
Phone:
866-572-6436
Sponsor
AMGEN CANADA INC

Locations

Quebec

Research Site
Chicoutimi, Quebec, G7H 5H6
Research Site
Chicoutimi, Quebec, G7H 7K9
Research Site
Québec, Quebec, G1V 4W2

Results

See the results from the trial NCT02392559. This is an external link. The information is not authorized by the Government of Canada.

Date posted:
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