80
Participants
Start Date
December 31, 2013
Primary Completion Date
November 30, 2017
Study Completion Date
November 30, 2017
Ibrutinib
All subjects will receive 560 mg of Ibrutinib orally.
rituximab
All subjects will receive rituximab 375 mg/m2 intravenously
Memorial Sloan-Kettering Cancer Center, New York
Weill Cornell Medical College New York-Presbyterian Hospital, New York
Southeastern Regional Medical Center, Newnan
Tennessee Oncology, PLLC The Sarah Cannon Research Institute, Nashville
Mid-Ohio Oncology/ Hematology Inc, Columbus
Community Health Network Community Regional Cancer Center North, Indianapolis
The University of Texas MD Anderson Cancer Center, Houston
Comprehensive Cancer Centers of Nevada, Henderson
UCLA Medical Center, Los Angeles
City of Hope, Duarte
Providence Saint Joseph Medical Center, Burbank
Stanford University, Stanford Care Center, Stanford
Lead Sponsor
Pharmacyclics LLC.
INDUSTRY