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.

CYRAMZA® (ramucirumab): Approval for Treatment of HCC

Cyramza (ramucirumab), as a single agent, is indicated for the treatment of HCC who have an AFP ≥400 ng/mL and have been treated with sorafenib.

Detailed Information

On May 10, 2019, the FDA approved ramucirumab as a single agent for the treatment of patients with HCC who have an AFP ≥400 ng/mL and have been treated with sorafenib therapy.1

Enclosed Prescribing Information

CYRAMZA® (ramucirumab) injection, for intravenous use, Lilly

Reference

1. Cyramza [package insert]. Indianapolis, IN: Eli Lilly and Company; 2019.

Glossary

AFP = alpha-fetoprotein

FDA = Food and Drug Administration 

HCC = hepatocellular carcinoma

Date of Last Review: March 28, 2019

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