공식 규제·평가 기관 출처를 바탕으로 한 국가별 승인·접근 상태입니다. 무엇이 어디에 존재하는지를 보여줄 뿐, 추천이 아닙니다.
European Union
Avelumab (Bavencio)[1]EMA authorisedNo biomarker requirement stated in fetched EMA Bavencio page; Adult metastatic Merkel cell carcinoma. · EMA central authorization does not establish reimbursement or availability in Germany, France, or other EU member states. No claim is made for localized MCC or pediatric use in the EU from this fetched source. Confidence/conflicts: High for EMA authorization text; member-state access remains a gap.
Avelumab (Bavencio)[1]EMA authorisedNo biomarker requirement stated in fetched EMA Bavencio page; Adult metastatic Merkel cell carcinoma. · EMA central authorization does not establish reimbursement or availability in Germany, France, or other EU member states. No claim is made for localized MCC or pediatric use in the EU from this fetched source. Confidence/conflicts: High for EMA authorization text; member-state access remains a gap.
United Kingdom
Avelumab (Bavencio)[2]ApprovedNo biomarker requirement stated in fetched NICE recommendation; Adults with untreated metastatic MCC who have not had chemotherapy for metastatic disease; post-chemotherapy routine NHS availability noted by NICE. · NICE recommendation is an England/Wales NHS appraisal context and includes a commercial arrangement. It does not establish MHRA label wording, Scotland/Northern Ireland status, or individual suitability. Confidence/conflicts: High for NICE recommendation text; devolved UK and MHRA label specifics remain active gaps.
Avelumab (Bavencio)[2]ApprovedNo biomarker requirement stated in fetched NICE recommendation; Adults with untreated metastatic MCC who have not had chemotherapy for metastatic disease; post-chemotherapy routine NHS availability noted by NICE. · NICE recommendation is an England/Wales NHS appraisal context and includes a commercial arrangement. It does not establish MHRA label wording, Scotland/Northern Ireland status, or individual suitability. Confidence/conflicts: High for NICE recommendation text; devolved UK and MHRA label specifics remain active 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.