Vatalanib (PTK787/ZK-222584) is a new oral antiangiogenic molecule that inhibits all known vascular endothelial growth factor receptors. Vatalanib is under investigation for the treatment of solid tumors. Disposition and biotransformation of vatalanib were studied in an open-label, single-center study in patients with advanced cancer. Seven patients were given a single oral (14)C-radiolabeled dose of 1,000 mg of vatalanib administered at steady state, obtained after 14 consecutive daily oral doses of 1,000 mg of nonradiolabeled vatalanib. Plasma, urine, and feces were analyzed for radioactivity, vatalanib, and its metabolites. Metabolite patterns were determined by high-performance liquid chromatography coupled to radioactivity detection wi...
Abstract Background Chiauranib is a novel orally active multi-target inhibitor that simultaneously i...
AbstractWe have recently reported that vatalanib, an orally active small molecule multi-tyrosine kin...
Purpose: To assess the maximum tolerated dose (MTD)/dose-limiting toxicities (DLT), safety, pharmaco...
Vatalanib (PTK787/ZK-222584) is a new oral antiangiogenic mole-cule that inhibits all known vascular...
Targeting angiogenesis in glioblastoma (GBM) may improve patient outcome by normalizing tumor vascul...
Background: Vatalanib is a selective inhibitor of vascular endothelial growth factor (VEGF) receptor...
PurposeVatalanib (PTK 787/ZK22584) is an oral poly-tyrosine kinase inhibitor with strong affinity fo...
Lenvatinib is an orally available multi-targeted tyrosine kinase inhibitor with anti-angiogenic and ...
PTK787/ZK222584 (Vatalanib), an orally active inhibitor of vascular endothelial growth factor recept...
Background A phase 2 study of vatalanib (PTK787/ZK222584) an oral tyrosine kinase inhibitor of VEGF...
Vandetanib, lenvatinib and cabozantinib are inhibitors of receptor tyrosine kinases approved to trea...
We have recently reported that vatalanib, an orally active small molecule multi-tyrosine kinase inhi...
BACKGROUND: Due to the hypervascular nature of glioblastoma (GBM), antiangiogenic treatments, such a...
PTK787/ZK 222584 (PTK/ZK) offers a novel approach to inhibit tumour angiogenesis.; This study charac...
Apatinib is a new oral antiangiogenic molecule that inhibits vascular endothelial growth factor rece...
Abstract Background Chiauranib is a novel orally active multi-target inhibitor that simultaneously i...
AbstractWe have recently reported that vatalanib, an orally active small molecule multi-tyrosine kin...
Purpose: To assess the maximum tolerated dose (MTD)/dose-limiting toxicities (DLT), safety, pharmaco...
Vatalanib (PTK787/ZK-222584) is a new oral antiangiogenic mole-cule that inhibits all known vascular...
Targeting angiogenesis in glioblastoma (GBM) may improve patient outcome by normalizing tumor vascul...
Background: Vatalanib is a selective inhibitor of vascular endothelial growth factor (VEGF) receptor...
PurposeVatalanib (PTK 787/ZK22584) is an oral poly-tyrosine kinase inhibitor with strong affinity fo...
Lenvatinib is an orally available multi-targeted tyrosine kinase inhibitor with anti-angiogenic and ...
PTK787/ZK222584 (Vatalanib), an orally active inhibitor of vascular endothelial growth factor recept...
Background A phase 2 study of vatalanib (PTK787/ZK222584) an oral tyrosine kinase inhibitor of VEGF...
Vandetanib, lenvatinib and cabozantinib are inhibitors of receptor tyrosine kinases approved to trea...
We have recently reported that vatalanib, an orally active small molecule multi-tyrosine kinase inhi...
BACKGROUND: Due to the hypervascular nature of glioblastoma (GBM), antiangiogenic treatments, such a...
PTK787/ZK 222584 (PTK/ZK) offers a novel approach to inhibit tumour angiogenesis.; This study charac...
Apatinib is a new oral antiangiogenic molecule that inhibits vascular endothelial growth factor rece...
Abstract Background Chiauranib is a novel orally active multi-target inhibitor that simultaneously i...
AbstractWe have recently reported that vatalanib, an orally active small molecule multi-tyrosine kin...
Purpose: To assess the maximum tolerated dose (MTD)/dose-limiting toxicities (DLT), safety, pharmaco...