The novel indole-ether quinazoline Cediranib is a highly potent (IC < 1 nmol/L) ATP-competitive inhibitor of recombinant KDR tyrosine kinase in vitro. It is being developed clinically as a once-daily oral therapy for the treatment of cancer.
For the treatment of liver cancer, advanced non-small cell lung cancer (NSCLC), advanced colorectal cancer (CRC) and other solid tumors.
M D Anderson Cancer Center, Houston, Texas, United States
Massachusetts General Hospital Cancer Center, Boston, Massachusetts, United States
National Institutes of Health Clinical Center, 9000 Rockville Pike, Bethesda, Maryland, United States
Massachusetts General Hospital Cancer Center, Boston, Massachusetts, United States
Wayne State University/Karmanos Cancer Institute, Detroit, Michigan, United States
University of Maryland/Greenebaum Cancer Center, Baltimore, Maryland, United States
Children's Hospital of Pittsburgh of UPMC, Pittsburgh, Pennsylvania, United States
Pediatric Brain Tumor Consortium, Memphis, Tennessee, United States
Duke University Medical Center, Durham, North Carolina, United States
Massachusetts General Hospital Cancer Center, Boston, Massachusetts, United States
Howard University Hospital, Washington, D.C., District of Columbia, United States
Dana-Farber Cancer Institute, Boston, Massachusetts, United States
North Central Cancer Treatment Group, Rochester, Minnesota, United States
Warren Grant Magnuson Clinical Center - NCI Clinical Studies Support, Bethesda, Maryland, United States
Cancer Institute of New Jersey at UMDNJ - Robert Wood Johnson Medical School, New Brunswick, New Jersey, United States
University of Chicago Comprehensive Cancer Center, Chicago, Illinois, United States
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