81
Participants
Start Date
May 26, 2016
Primary Completion Date
November 8, 2018
Study Completion Date
December 3, 2024
BAY1436032
The selected starting dose of BAY1436032 is 300 mg/day (150 mg BID) to be administered orally continuously in tablet form in 21-day cycles. Adjustments to this schedule may be made if warranted by information collected during the course of the study. The maximum feasible dose of BAY1436032 is expected to be 3000 mg/day.
København Ø
Charlottesville
Essen
Frankfurt am Main
Heidelberg
Tübingen
Houston
München
Los Angeles
Los Angeles
Nagoya
Kashiwa
Chuo-ku
Lead Sponsor
Bayer
INDUSTRY