53
Participants
Start Date
March 31, 2008
Primary Completion Date
May 31, 2012
Study Completion Date
November 30, 2014
Sorafenib
Sorafenib 400 mg twice daily by mouth Study treatment will be given in cycles of 28 days. Patients will be re-staged every 2 treatment cycles (every 8 weeks). Patients with an objective response or stable disease will continue study treatment. Patients will continue until disease progression or intolerable toxicity occurs.
Erlotinib
Erlotinib 150 mg once daily by mouth
Center for Cancer and Blood Disorders, Bethesda
National Capital Clinical Research Consortium, Bethesda
Wellstar Cancer Research, Marietta
Northeast Georgia Medical Center, Gainesville
Florida Cancer Specialists, Fort Myers
Tennessee Oncology, PLLC, Nashville
Associates in Hematology Oncology, Chattanooga
Chattanooga Oncology Hematology Associates, Chattanooga
Jackson Oncology Associates, Jackson
Norton Cancer Institute, Louisville
Providence Medical Group, Terre Haute
St. Louis Cancer Care, Chesterfield
Research Medical Center, Kansas City
Nebraska Methodist Cancer Center, Omaha
Hematology Oncology Clinic, LLP, Baton Rouge
Hematology-Oncology Associates of Northern NJ, Morristown
Collaborators (2)
Bayer
INDUSTRY
OSI Pharmaceuticals
INDUSTRY
SCRI Development Innovations, LLC
OTHER