11
Participants
Start Date
February 21, 2013
Primary Completion Date
October 17, 2016
Study Completion Date
January 9, 2019
Nilotinib
"Participants will remain on the same dose of nilotinib they have been receiving prior to enrollment on the trial. This will range from 300 mg PO BID to 400 mg PO BID.~Dose modifications will not occur, as the purpose of this study is to determine the maximum tolerated dose of ruxolitinib, based on the number of dose."
Ruxolitinib
Dose escalation will follow a 3+3 study design. Dose modifications will not occur, as the purpose of this study is to determine the maximum tolerated dose, based on the number of dose limiting toxicities seen at a specific dose.
H. Lee Moffitt Cancer Center and Research Institute, Tampa
Collaborators (1)
Incyte Corporation
INDUSTRY
H. Lee Moffitt Cancer Center and Research Institute
OTHER