20
Participants
Start Date
March 24, 2015
Primary Completion Date
July 27, 2016
Study Completion Date
July 27, 2016
BAY1187982
A dose of 0.1 mg BAY 1187982 per kilogram (kg) body weight (BW) was chosen as the starting dose based on toxicology data. The investigational drug will be administered as a 1-hour IV infusion once every 21 days at the trial site (Day 1 of each 21-day Cycle). The maximum possible dose escalation will be 2-fold and not more than 0.5 mg/kg BW until maximum tolerated dose is selected
New York
Baltimore
Nashville
Chicago
St Louis
Houston
San Francisco
Singapore
Santa Monica
New Haven
Seattle
Seoul
Seoul
Lead Sponsor
Bayer
INDUSTRY