Safety and Pharmacokinetics of IGSC 20% in Subjects With Primary Immunodeficiency

Last updated:
2026-07-11
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View trial details

Overview

Official protocol title:

AN OPEN-LABEL, MULTI-CENTER STUDY TO EVALUATE THE SAFETY AND PHARMACOKINETICS OF IGSC 20% ADMINISTERED FOR 6 MONTHS IN SUBJECTS WITH PRIMARY IMMUNODEFICIENCY

Intervention/treatment:
IGSC 20%, IMMUNE GLOBULIN SUBCUTANEOUS (HUMAN), 20% CAPRYLATE/CHROMATOGRAPHY PURIFIED
Medical condition:
PRIMARY IMMUNODEFICIENCY DISEASES
Protocol code:
GTI1502
Control number:
187988
Status:
Closed
Approved:
October 23, 2015
Date Completed:
Trial phase:
Phase 3
For more information:
ClinicalTrials.gov - NCT02604810
This is an external link. The information is not authorized by the Government of Canada.

Eligibility

Sex: ALL
Age
2 Years to 75 Years
Accepts healthy volunteers: No

Contacts and locations

Contact
Name
Rhonda Griffin
Organization
Grifols Therapeutics LLC
Phone:
919-316-6693
Sponsor
GRIFOLS THERAPEUTICS INC

Locations

Clinique d'asthme et d'allergie de Quebec
Québec, G1V 4M6
The Hospital for Sick Children
Toronto, M5G 1X8

Ontario

McGill University Health Center
Montreal, Ontario, H4A 3J1
Ottawa Hospital, Division of Infectious Disease and Respirology
Ottawa, Ontario, K1H 8L6

Quebec

CHU Sainte-Justine
Montreal, Quebec, H3T 1C4

Results

See the results from the trial NCT02604810. This is an external link. The information is not authorized by the Government of Canada.

Date posted:
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