Stivarga

regorafenib · Bayer Pharma AG
AUTHORISED IN THE EU

What Stivarga is used for

Stivarga is indicated as monotherapy for the treatment of adult patients with: metastatic colorectal cancer (CRC) who have been previously treated with, or are not considered candidates for, available therapies - these include fluoropyrimidine-based chemotherapy, an anti-VEGF therapy and an anti-EGFR therapy; unresectable or metastatic gastrointestinal stromal tumors (GIST) who progressed on or are intolerant to prior treatment with imatinib and sunitinib; hepatocellular carcinoma (HCC) who have been previously treated with sorafenib.

Approved use, as published by the European Medicines Agency.

Key facts

Brand
Stivarga
Active substance
regorafenib
Disease area
Colorectal Neoplasms
Medicine group
Antineoplastic agents;Protein kinase inhibitors
ATC code
L01EX05
Marketing authorisation holder
Bayer Pharma AG
Authorised in the EU since
2013

Official information

In the USA

Same active substance: Stivarga

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 Stivarga used for?

Stivarga is indicated as monotherapy for the treatment of adult patients with: metastatic colorectal cancer (CRC) who have been previously treated with, or are not considered candidates for, available therapies - these include fluoropyrimidine-based chemotherapy, an anti-VEGF therapy and an anti-EGFR therapy; unresectable or metastatic gastrointestinal stromal tumors (GIST) who progressed on or are intolerant to prior treatment with imatinib and sunitinib; hepatocellular carcinoma (HCC) who have been previously treated with sorafenib.

What is the active substance in Stivarga?

Stivarga contains regorafenib.

Who makes Stivarga?

The EU marketing authorisation holder is Bayer Pharma AG.

Source: European Medicines Agency medicines data (ema.europa.eu), reproduced with acknowledgement of the source. Page made 5 November 2026 by Satya Babu.

← All specialty medicines, EU

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