Safety and Tolerability of Higher Infusion Parameters of IgPro20 (Hizentra) in Subjects With Primary Immunodeficiency (PID)

PHASE4CompletedINTERVENTIONAL
Enrollment

49

Participants

Timeline

Start Date

February 1, 2017

Primary Completion Date

December 14, 2018

Study Completion Date

December 14, 2018

Conditions
Primary Immunodeficiency
Interventions
DRUG

IgPro20

A liquid formulation of normal human IgG at a concentration of 20% administered as a subcutaneous infusion at a dose prescribed by subject's physician prior to study entry.

Trial Locations (12)

10029

Icahn Medical Institute, New York

11021

Long Island Jewish Medical Center, Great Neck

14607

Center for Clinical Research Rochester General Hospital, Rochester

27705

Duke University School of Medicine, Durham

28203

Levine Children's Hospital, Charlotte

31707

Georgia Pollens Clinical Research Centers, Albany

33701

University of Southern Florida, St. Petersburg

35209

Clinical Research Center of Alabama, Birmingham

53226

Medical College of Wisconsin, Milwaukee

85340

Research Solutions of Arizona, Litchfield Park

K1H 8L6

The Ottawa Hospital, Ottawa

H4A3J1

McGill University, Montreal

Sponsors

Lead Sponsor

All Listed Sponsors
lead

CSL Behring

INDUSTRY