This study will evaluate safety and efficacy of TKI258 in patients with relapsed or refractory multiple myeloma
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
TREATMENT
Masking
NONE
Enrollment
43
Overall response rate
Time frame: 4 weeks
frequency and severity of adverse events as per CTCAE
Time frame: throughout the study
Progression free survival (PFS)
Time frame: every 4 weeks
Plasma exposure of TKI258
Time frame: during the first 3 cycles
This platform is for informational purposes only and does not constitute medical advice. Always consult a qualified healthcare professional.
University of South Alabama / Mitchell Cancer Institute Dept. of Mitchell Cancer Inst.
Mobile, Alabama, United States
Central Hematology Oncology Medical Group
Alhambra, California, United States
Central Coast Medical Oncology Corporation
Santa Maria, California, United States
St. Jude Heritage Medical Group Virginia Crosson Cancer Center
Yorba Linda, California, United States
Kootenai Medical Center Kootenai Medical Center
Coeur d'Alene, Idaho, United States
Hematology and Oncology Specialists Dept of Hem&Onc Specialist - 2
Metairie, Louisiana, United States
Mayo Clinic - Rochester Rochester
Rochester, Minnesota, United States
Memorial Sloan Kettering Cancer Center MSKCC
New York, New York, United States
Duke University Medical Center Dept. of DUMC (4)
Durham, North Carolina, United States
Lancaster Cancer Center
Lancaster, Pennsylvania, United States
...and 20 more locations