31
Participants
Start Date
December 31, 2014
Primary Completion Date
June 29, 2017
Study Completion Date
June 29, 2017
MSC2490484A (M3814)
Participants received MSC2490484A capsules at escalated dose from 100 mg to 400 mg orally from Day 1 to Day 21 of each treatment cycle until disease progression, unacceptable toxicity, withdrawal of consent, and/or occurrence of any criterion for withdrawal from study or M3814.
Institut Jules Bordet, Brussels
UZ Leuven, Leuven
Rigshospitalet - Onkologisk KFE, Copenhagen
Herlev Hospital University of Copenhagen, Herlev
Antoni van Leeuwenhoek Ziekenhuis, Amsterdam
VU Medisch Centrum - Dept of Medical Oncology, Amsterdam
Erasmus Medisch Centrum - Parent, Rotterdam
Merck KGaA, Darmstadt, Germany
INDUSTRY