88
Participants
Start Date
November 5, 2019
Primary Completion Date
April 20, 2022
Study Completion Date
August 15, 2022
Canakinumab
200 mg of canakinumab administered via subcutaneous injections once every 3 weeks for a maximum duration of 6 weeks
Pembrolizumab
200 mg of pembrolizumab administered via infusion once every 3 weeks for a maximum duration of 6 weeks
Novartis Investigative Site, Taipei
Novartis Investigative Site, Brussels
Novartis Investigative Site, 's-Hertogenbosch
SUNY - Upstate Medical University, Syracuse
Novartis Investigative Site, Jaén
Novartis Investigative Site, Madrid
Novartis Investigative Site, Oviedo
Novartis Investigative Site, Montpellier
Novartis Investigative Site, Giessen
Novartis Investigative Site, Cologne
Novartis Investigative Site, Sakarya
Novartis Investigative Site, Thessaloniki
University of Kansas Medical Center Neurology Dept., Kansas City
Novartis Investigative Site, Bron
Novartis Investigative Site, Paris
Methodist Hospital / Methodist Cancer Center, Houston
UCLA Oncology Hematology, La Jolla
Novartis Investigative Site, Bad Berka
Novartis Investigative Site, Taipei
Novartis Investigative Site, Saint Petersburg
Novartis Investigative Site, Saint Petersburg
Novartis Investigative Site, Omsk
Novartis Investigative Site, Montreal
Novartis Investigative Site, Halle
Novartis Investigative Site, Kashiwa
Novartis Investigative Site, Breda
Novartis Investigative Site, Maastricht
Novartis Investigative Site, Izmir
Novartis Investigative Site, Sihhiye / Ankara
Lead Sponsor
Novartis Pharmaceuticals
INDUSTRY