4
Participants
Start Date
August 24, 2015
Primary Completion Date
April 8, 2016
Study Completion Date
August 31, 2016
Copanlisib (BAY80-6946)
Starting dose 60 mg (dose reduction due to toxicities to 45 mg allowed). Administered in slow IV bolus on days 1, 8 and 15 of each 28 day cycle until disease progression or until another criterion is met for withdrawal from study treatment.
New York
New York
Baltimore
Hackensack
Burlington
Lead Sponsor
Bayer
INDUSTRY