Evolocumab Compared to LDL-C Apheresis in Patients Receiving LDL-C Apheresis Prior to Study Enrollment

PHASE3CompletedINTERVENTIONAL
Enrollment

39

Participants

Timeline

Start Date

December 21, 2015

Primary Completion Date

September 1, 2016

Study Completion Date

January 20, 2017

Conditions
Hypercholesterolemia
Interventions
BIOLOGICAL

Evolocumab

Administered by subcutaneous injection once every 2 weeks

PROCEDURE

Low-density Lipoprotein Cholesterol (LDL-C) Apheresis

Participants received apheresis for LDL-C according the their physician's prescription and local custom.

Trial Locations (17)

3084

Research Site, Heidelberg

13353

Research Site, Berlin

24939

Research Site, Flensburg

33434

Research Site, Boca Raton

40210

Research Site, Düsseldorf

41013

Research Site, Seville

44093

Research Site, Nantes

49418

Research Site, Grandville

56124

Research Site, Pisa

66160

Research Site, Kansas City

69677

Research Site, Bron

97239

Research Site, Portland

500 05

Research Site, Hradec Králové

01307

Research Site, Dresden

00161

Research Site, Roma

UB9 6JH

Research Site, Harefield

CF64 2XX

Research Site, Penarth

Sponsors

Lead Sponsor

All Listed Sponsors
lead

Amgen

INDUSTRY