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Cyramza ® (ramucirumab) injection
10 mg/mL solution
This information is provided in response to your request. Resources may contain information about doses, uses, formulations and populations different from product labeling. See Prescribing Information above, if applicable.
Ramucirumab: Approval for Treatment of NSCLC
In the US, ramucirumab, in combination with erlotinib, is indicated for the first-line treatment of patients with metastatic NSCLC whose tumors have EGFR exon 19 deletions or exon 21 (L858R) substitution mutations.
On May 29, 2020, the FDA approved ramucirumab, in combination with erlotinib, for the first-line treatment of patients with metastatic NSCLC whose tumors have EGFR exon 19 deletions or exon 21 (L858R) substitution mutations.1
Enclosed Prescribing Information
1Cyramza [package insert]. Indianapolis, IN: Eli Lilly and Company; 2020.
EGFR = epidermal growth factor receptor
FDA = Food and Drug Administration
NSCLC = non-small cell lung cancer
Date of Last Review: May 29, 2020