36
Participants
Start Date
June 13, 2018
Primary Completion Date
September 29, 2021
Study Completion Date
March 29, 2022
BAY2287411
"Dose Escalation part:~A single dose will be administered intravenously on Day 1 of each cycle lasting 6 weeks (42 days)."
BAY2287411
"Dose Expansion part:~The selection of the dose level(s) /regimen(s) to be evaluated will be based on the overall benefit / risk and PK profile observed in the dose escalation."
National Cancer Institute - Maryland, Bethesda
University of Texas MD Anderson Cancer Center, Houston
HUS, Meilahden sairaala, Helsinki
Nederlands Kanker Instituut, Amsterdam
Universitair Medisch Centrum Groningen, Groningen
Skånes Universitetssjukhus, Lund
Royal Marsden NHS Trust (Surrey), Sutton
Lead Sponsor
Bayer
INDUSTRY