공식 규제·평가 기관 출처를 바탕으로 한 국가별 승인·접근 상태입니다. 무엇이 어디에 존재하는지를 보여줄 뿐, 추천이 아닙니다.
European Union
Retifanlimab (Zynyz) with carboplatin and paclitaxel[1]EMA authorisedNo biomarker requirement stated in fetched EMA news source; Adults with SCAC that cannot be removed by surgery and is metastatic or locally recurrent, in combination with carboplatin and paclitaxel. · The fetched EMA source is a recommendation/news page, not final EPAR product information; European Commission authorization status and member-state reimbursement must be verified separately. No claim is made for monotherapy EU use from this source. Confidence/conflicts: Medium-high for EMA CHMP recommendation; final authorization and country access remain follow-up gaps.
Retifanlimab (Zynyz) with carboplatin and paclitaxel[1]EMA authorisedNo biomarker requirement stated in fetched EMA news source; Adults with SCAC that cannot be removed by surgery and is metastatic or locally recurrent, in combination with carboplatin and paclitaxel. · The fetched EMA source is a recommendation/news page, not final EPAR product information; European Commission authorization status and member-state reimbursement must be verified separately. No claim is made for monotherapy EU use from this source. Confidence/conflicts: Medium-high for EMA CHMP recommendation; final authorization and country access remain follow-up gaps.
Retifanlimab (Zynyz) with carboplatin and paclitaxel[1]EMA authorisedNo biomarker requirement stated in fetched EMA news source; Adults with SCAC that cannot be removed by surgery and is metastatic or locally recurrent, in combination with carboplatin and paclitaxel. · The fetched EMA source is a recommendation/news page, not final EPAR product information; European Commission authorization status and member-state reimbursement must be verified separately. No claim is made for monotherapy EU use from this source. Confidence/conflicts: Medium-high for EMA CHMP recommendation; final authorization and country access remain follow-up gaps.
위 내용은 공식 규제·접근 상태일 뿐, 의학적 조언이나 추천이 아니고, 적격성을 판단하지도 않습니다. 어떤 선택지가 적합한지는 환자의 상황과 종양내과 팀에 달려 있습니다. 규제 상태는 바뀔 수 있으니 표시된 출처에서 확인하세요. 임상 세부 내용은 영문이 정본입니다. 최종 확인 2026-06-12.