Regorafenib tablets | China Drugs List
Public reference information, not medical advice, a prescription or an offer to supply a medicine. Confirm current approval, availability and suitability with licensed professionals.
Others
- Brand
- Stivarga
- Company
- Bayer Pharma AG (EU authorization holder)
- Medicine type
- Chemical medicine
- Therapeutic area
- Oncology
- Indications recorded in the public source
- Selected EU indications: Monotherapy for adults with metastatic colorectal cancer after available therapies or when these are unsuitable, including fluoropyrimidine chemotherapy and anti-VEGF and anti-EGFR therapy. Also for unresectable or metastatic gastrointestinal stromal tumors after progression or intolerance on imatinib and sunitinib, and hepatocellular carcinoma after sorafenib. This summary does not establish the approved indications in China.
- Indication source and scope
- Web page accessed 2026-11-02. Selected overseas indications; does not establish the Chinese approved scope.
- Prescribing-information limitations
- Regulatory product information / approval evidence is linked; a complete current prescribing-information document has not been verified in this review.
- China availability status
- Chinese approval, current Chinese indications and continuous market availability were not independently verified in this English-source review.
- Overseas status
- See the linked overseas regulator / manufacturer evidence. Approval and indications are jurisdiction-specific; current supply is not established.
- Insurance classification
- Not yet verified
- Insurance edition
- Chinese national insurance review pending
- Insurance verification notes
- No reimbursement determination was made for this addition; missing information is not proof of exclusion.
Sources
- https://www.ema.europa.eu/en/medicines/human/EPAR/stivarga
- Stivarga — EMA European public assessment report
Regulatory medicine overview · Web page accessed 2026-11-02
English primary regulatory source opened and reviewed. Selected EU indications and the EU authorization holder are reported; this is not evidence of Chinese approval.
Evidence reviewed:
Open the interactive record, public price references and discussions