Talazoparib capsules | 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
- Talzenna
- Company
- Pfizer Europe MA EEIG (EU authorization holder)
- Medicine type
- Chemical medicine
- Therapeutic area
- Oncology
- Indications recorded in the public source
- EU: Used alone for adults with germline BRCA1/2-mutated, HER2-negative locally advanced or metastatic breast cancer after an anthracycline and/or taxane unless unsuitable; hormone receptor-positive disease also requires prior endocrine therapy or unsuitability. With enzalutamide for adults with metastatic castration-resistant prostate cancer when chemotherapy is not clinically indicated.
- Indication source and scope
- EU SmPC accessed 2026-11-02; current linked revision. Selected overseas indications; does not establish the Chinese approved scope.
- Prescribing-information limitations
- Overseas official prescribing information linked; a complete current Chinese label has not been verified.
- China availability status
- Chinese approval, locally approved indications and current availability have not been independently verified in this import.
- 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/documents/product-information/talzenna-epar-product-information_en.pdf
- Talzenna — official prescribing information
Official prescribing information · EU SmPC accessed 2026-11-02; current linked revision
English primary source reviewed. This evidence describes the cited overseas jurisdiction and does not verify Chinese approval, indications, reimbursement or market availability.
Evidence reviewed:
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