176
Participants
Start Date
August 31, 2011
Primary Completion Date
June 30, 2015
Study Completion Date
June 30, 2015
brentuximab vedotin
1.8 mg/kg every 3 weeks by IV infusion
rituximab
375 mg/m2 every 3 weeks by IV infusion
NYU Clinical Cancer Center, New York
Columbia University Medical Center, New York
Memorial Sloan Kettering Cancer Center, New York
New York Oncology Hematology, P.C., Albany
Virginia Cancer Specialists, PC, Fairfax
Medical University of South Carolina, Charleston
St. Francis Hospital, Greenville
Emory Winship Cancer Institute, Atlanta
Cancer Specialists of North Florida - St. Augustine, Saint Augustine
Cleveland Clinic, The, Cleveland
Minnesota Oncology Hematology P.A., Minneapolis
Northwestern University, Chicago
Washington University School of Medicine, St Louis
Texas Oncology - Medical City Dallas, Dallas
Charles A. Sammons Cancer Center, Dallas
Texas Oncology - Tyler, Tyler
Texas Oncology-Southwest Fort Worth, Fort Worth
Texas Oncology - Seton Williamson, Round Rock
Rocky Mountain Cancer Centers - Aurora, Aurora
Colorado Blood Cancer Institute, Denver
Comprehensive Cancer Centers of Nevada, Las Vegas
PMK Medical Group Inc., DBA Ventura County Hematology Oncology Specialists, Oxnard
Willamette Valley Cancer and Research / USOR, Eugene
Swedish Cancer Institute Medical Oncology, Edmonds
Seattle Cancer Care Alliance / University of Washington Medical Center, Seattle
Northwest Cancer Specialists, P.C., Vancouver
University of Alabama at Birmingham, Birmingham
City of Hope, Duarte
Stanford Cancer Center, Stanford
University of Chicago, Chicago
Dana-Farber Cancer Institute, Boston
Hackensack University Medical Center, Hackensack
MD Anderson Cancer Center / University of Texas, Houston
British Columbia Cancer Agency - Vancouver Centre, Vancouver
Seagen Inc.
INDUSTRY