19
Participants
Start Date
May 7, 2015
Primary Completion Date
March 7, 2017
Study Completion Date
August 1, 2018
Canakinumab
canakinumab was provided as a 150 mg/1 mL solution for subcutaneous injection and administered at 4mg/kg every 4 weeks.
Novartis Investigative Site, Ōbu
Novartis Investigative Site, Chiba
Novartis Investigative Site, Kanazawa
Novartis Investigative Site, Kagoshima
Novartis Investigative Site, Yokohama
Novartis Investigative Site, Yokohama
Novartis Investigative Site, Sendai
Lead Sponsor
Novartis Pharmaceuticals
INDUSTRY