116
Participants
Start Date
February 14, 2017
Primary Completion Date
August 10, 2018
Study Completion Date
May 13, 2020
PDR001
PDR001 was administered at a dose of 400 mg via intravenous infusion once every 4 weeks (Q4W). PDR001 was administered on Day 1 of every cycle. Each cycle was 28 days.
Novartis Investigative Site, St Leonards
Novartis Investigative Site, Leuven
Memorial Sloan Kettering Cancer Center, New York
Montefiore Medical Center, The Bronx
Novartis Investigative Site, Marseille
Novartis Investigative Site, Milan
Novartis Investigative Site, Milan
Novartis Investigative Site, Madrid
Novartis Investigative Site, Madrid
Novartis Investigative Site, Toulouse
H Lee Moffitt Cancer Center and Research Institute, Tampa
Novartis Investigative Site, Marburg
Novartis Investigative Site, Bologna
Novartis Investigative Site, Essen
Novartis Investigative Site, Meldola
Novartis Investigative Site, Mainz
Mayo Clinic - Rochester, Rochester
Novartis Investigative Site, Lyon
University of TX MD Anderson Cancer Center, Houston
Novartis Investigative Site, Napoli
Rocky Mountain Cancer Centers SC-2, Denver
City of Hope National Medical Center, Duarte
Novartis Investigative Site, Erlangen
Novartis Investigative Site, Vienna
Novartis Investigative Site, Brussels
Novartis Investigative Site, Toronto
Novartis Investigative Site, Montreal
Novartis Investigative Site, Roma
Novartis Investigative Site, Nagoya
Novartis Investigative Site, Kashiwa
Novartis Investigative Site, Fukuoka
Novartis Investigative Site, Chuo Ku
Novartis Investigative Site, Amsterdam
Novartis Investigative Site, L'Hospitalet de Llobregat
Novartis Investigative Site, London
Lead Sponsor
Novartis Pharmaceuticals
INDUSTRY