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
Princess Margaret Cancer Centre, Toronto, Ontario, Canada
Addenbrooke's Hospital, Cambridge, England, United Kingdom
Beatson Institute for Cancer Research, Glasgow, United Kingdom
Case Western Reserve University, Cleveland, Ohio, United States
Sutter Cancer Centers Radiation Oncology Services-Auburn, Auburn, California, United States
Kaiser Permanente-Baldwin Park, Baldwin Park, California, United States
Velindre Cancer Centre, Velindre University NHS Trust, Cardiff, United Kingdom
Royal United Hospitals Bath NHS Foundation Trust, Bath, United Kingdom
Bristol Haematology & Oncology Centre, University Hospitals Bristol NHS Foundation Trust, Bristol, United Kingdom
Research Site, Sevilla, Spain
Spedali Civili di Brescia, Brescia, BS, Italy
Istituto Oncologico Veneto (IOV), Padova, PD, Italy
Arcispedale Santa Maria Nuova, Reggio Emilia, RE, Italy
Calvary Mater Hospital, Sydney, New South Wales, Australia
Campbelltown Hospital, Sydney, New South Wales, Australia
Prince of Wales Hospital, Sydney, New South Wales, Australia
Royal Marsden Chelsea & Sutton, London, United Kingdom
The Christie, Manchester, United Kingdom
Royal Surrey County Hospital, Guildford, Surrey, United Kingdom
Massachusetts General Hospital Cancer Center, Boston, Massachusetts, United States
University of Pittsburgh Cancer Institute (UPCI), Pittsburgh, Pennsylvania, United States
UC San Diego Moores Cancer Center, La Jolla, California, United States
Stay informed with timely notifications on clinical trials, regulatory changes, and research advancements related to this medication.