67
Participants
Start Date
May 8, 2015
Primary Completion Date
July 5, 2016
Study Completion Date
January 19, 2018
Copanlisib (Aliqopa, BAY80-6946)
Participants assigned to receive copanlisib intravenous (IV) infusion at a dose of 60 mg as single agent on Days 1, 8, and 15 of 28-day treatment cycle. Copanlisib treatment was to be continued until disease progression (PD), unacceptable toxicity, or until another criterion was met for withdrawal from the study treatment
Bruxelles - Brussel
Wilrijk
Edegem
Kingswood
Leuven
Box Hill
Prahran
Ballarat
Odense C
Aarhus C
Ghent
Berlin
Caen
Milan
Münster
Lille
Pierre-Bénite
Paris
Poitiers
Créteil
Singapore
St. John's
Brampton
Montreal
Montreal
Sherbrooke
Leipzig
Seoul
Seoul
Truro
Southampton
London
Lead Sponsor
Bayer
INDUSTRY