Cyramza

Ramucirumab · Eli Lilly and Company
CANCER MEDICINE · PRESCRIPTION ONLY (USA)

Cyramza ingredients

Active ingredientStrength
Ramucirumab10 mg/mL

What Cyramza is used for

The FDA lists the approved uses on the official label (below). In the EU, ramucirumab is approved as Cyramza for:

Gastric cancer Cyramza in combination with paclitaxel is indicated for the treatment of adult patients with advanced gastric cancer or gastro-oesophageal junction adenocarcinoma with disease progression after prior platinum and fluoropyrimidine chemotherapy. Cyramza monotherapy is indicated for the treatment of adult patients with advanced gastric cancer or gastro-oesophageal junction adenocarcinoma with disease progression after prior platinum or fluoropyrimidine chemotherapy, for whom treatment in combination with paclitaxel is not appropriate. Colorectal cancer Cyramza, in combination with FOLFIRI (irinotecan, folinic acid, and 5-fluorouracil), is indicated for the treatment of adult patients with metastatic colorectal cancer (mCRC) with disease progression on or after prior therapy with bevacizumab, oxaliplatin and a fluoropyrimidine. Non-small cell lung cancer Cyramza in combination…

EU wording from the European Medicines Agency; US approved uses can differ.

Key facts

Brand
Cyramza
Generic name
Ramucirumab
Made by
Eli Lilly and Company
Forms
Solution
Given
Intravenous
Drug class
Vascular Endothelial Growth Factor Receptor 2 Antagonist
FDA approval
Biologic licence (BLA) BLA125477
On the US market since
2014

Official information

In India

Specialist medicine: started and supervised by a specialist doctor or hospital. This page is a plain-language summary of public official information, not medical advice; follow your doctor and the official product information.

Common questions

What is Cyramza?

Cyramza (Ramucirumab) is a cancer medicine made by Eli Lilly and Company, approved by the US FDA.

What are the ingredients of Cyramza?

Cyramza contains Ramucirumab (10 mg/mL).

Is Cyramza approved in Europe?

The same active substance is approved in the EU as Cyramza.

From the FDA National Drug Code directory (open.fda.gov, public domain) and the European Medicines Agency medicines list. Page made 5 November 2026 by Satya Babu.

← All specialty medicines, USA

For information only, not medical advice. This page is a plain-language summary written from standard prescribing information and the public guides linked below. Brands sometimes change their formula, so always check the composition printed on the pack. Doses here are typical adult doses; yours may differ. Do not start, stop or change a medicine without your doctor or pharmacist, and keep all medicines away from children. In an emergency, call 112 (India) or your local emergency number.