Drug intelligence / Profile preview

cediranib + lomustine

Development stage
Unknown
Lead developer
AstraZeneca
Modality
Small Molecules
Administration
Oral
01

Overview

Cediranib + lomustine is a combination therapy investigated for the treatment of recurrent glioblastoma. Cediranib is an oral small molecule inhibitor targeting vascular endothelial growth factor (VEGF) receptors, thereby inhibiting angiogenesis in tumors. Lomustine is an oral alkylating agent from the nitrosourea class that induces DNA cross-linking and damage, leading to cell death. The combination was evaluated in phase III clinical trials to determine if it improved progression-free survival compared to standard therapy with lomustine alone. While the combination showed some secondary benefits such as delayed neurologic deterioration and corticosteroid-sparing effects, it did not significantly improve progression-free or overall survival compared to monotherapy with lomustine[1][3][6].

Brand names
Recentin + lomustineCeeNu (for lomustine)
Other names
cediranib maleate + lomustinecediranib hydrochloride + lomustine
02

Targets

VEGFR2 (Vascular endothelial growth factor receptor 2)VEGFR-1 (Vascular endothelial growth factor receptor 1)VEGFR3 (Vascular endothelial growth factor receptor 3)DNA

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