166
Participants
Start Date
May 31, 2008
Primary Completion Date
April 30, 2010
Study Completion Date
April 30, 2010
Canakinumab (ACZ885)
6 mL glass vial containing 150 mg lyophilized Canakinumab reconstituted with water for a subcutaneous injection every 8 weeks. Dosage based on body weight.
Allergy Center at Brookstone, Columbus
Cleveland Clinic, Cleveland
University of Wisconsin, Madison
Rush-Presbyterian St. Lukes Medical Center, Chicago
Little Rock Allergy and Asthma Clinic, Little Rock
UCSF School of Medicine, San Francisco
Novartis Investigative Site, Laken
Novartis Investigative Site, Le Kremlin-Bicêtre
Novartis Investigative Site, Lille
Novartis Investigative Site, Montpelier Cedex
Novartis Investigative site, Nantes
Novartis Investigative site, Berlin
Novartis Investigative Site, Hamburg
Novartis Investigative site, Heidelberg
Novartis Investigative Site, Herne
Novartis Investigative Site, Marburg
Novartis Investigative site, Tübingen
Novartis Investigative site, New Delhi
Novartis Investigative site, Genova
Novartis Investigative Site, Napoli
Novartis Investigative Site, Padua
Novartis Investigative Site, Rome
Novartis Investigative Site, Trieste
Novartis Investigative Site, Madrid
Novartis Investigative site, Oviedo
Novartis Investigative Site, Vigo
Novartis Investigative site, Istanbul
Novartis Investigative site, London
Lead Sponsor
Novartis
INDUSTRY