Drug intelligence / Profile preview

osimertinib + ramucirumab

Development stage
Unknown
Lead developer
AstraZeneca
Modality
Monoclonal Antibodies → Antibody-Based Therapeutics, Small Molecules
Administration
Oral, Intravenous
01

Overview

Osimertinib + ramucirumab is a combination therapy under investigation for the treatment of advanced non-small cell lung cancer (NSCLC) with epidermal growth factor receptor (EGFR) mutations. Osimertinib is a third-generation, irreversible EGFR tyrosine kinase inhibitor that selectively targets both EGFR-sensitizing and T790M resistance mutations. Ramucirumab is a human IgG1 monoclonal antibody that inhibits angiogenesis by binding to vascular endothelial growth factor receptor 2 (VEGFR2), blocking its activation by VEGF ligands. The rationale for combining these agents is to simultaneously inhibit tumor cell proliferation via EGFR blockade and suppress tumor angiogenesis via VEGF pathway inhibition, potentially delaying resistance mechanisms and improving clinical outcomes. Clinical trials have shown this combination significantly prolongs progression-free survival compared to osimertinib alone in patients with TKI-naïve EGFR-mutant NSCLC, with an acceptable safety profile[1][2][3][6].

Brand names
Tagrisso (osimertinib)Cyramza (ramucirumab)
Other names
osimertinib plus ramucirumabramucirumab plus osimertinib
02

Targets

VEGFR2 (Vascular endothelial growth factor receptor 2)EGFR T790M (Epidermal growth factor receptor T790M mutant)

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