CYRAMZA® (Ramucirumab)

The FDA on December 12, 2014 approved CYRAMZA® for use in combination with TAXOTERE® (Docetaxel) for the treatment of patients with metastatic Non Small Cell Lung Cancer (NSCLC) with disease progression on or after platinum-based chemotherapy. Patients with EGFR or ALK genomic tumor aberrations should have disease progression on FDA-approved therapy for these aberrations prior to receiving CYRAMZA®. CYRAMZA® injection for intravenous infusion is a product of Eli Lilly and Company.