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基石藥業-B(02616.HK):高選擇性RET抑制劑普吉華®(Pralsetinib)在中國台灣獲批用於治療晚期RET融合非小細胞肺癌和RET變異甲狀腺癌
格隆匯 01-17 08:05

格隆匯1月17日丨基石藥業-B(02616.HK)發佈公吿,高選擇性RET抑制劑普吉®(Pralsetinib)在中國台灣獲批,用於治療局部晚期或轉移的轉染重排(“RET”)融合陽性非小細胞肺癌(“NSCLC”)、需接受全身性治療的晚期或轉移的RET突變甲狀腺髓樣癌(“MTC”)以及需接受全身性治療且經放射性碘治療無效(如適用放射性碘治療)的晚期或轉移的RET融合陽性甲狀腺癌成人患者。

普吉華®是一種強效、選擇性RET抑制劑,由基石藥業合作伙伴Blueprint Medicines公司開發。基石藥業與Blueprint Medicines公司達成了獨家合作和許可協議,獲得普拉替尼在大中華地區的獨家開發和商業化權利。

基石藥業首席執行官兼執行董事楊建新博士表示:“我們非常高興地看到繼泰時維®獲批用於治療晚期攜帶PDGFRAD842V突變的胃腸道間質瘤患者後,又一款重磅精準藥物普吉華®成功在中國台灣獲批上市。普吉華®已經在大中華區的多個地區獲批上市,具有優越和持久的臨牀抗腫瘤活性,整體安全可控。此次普吉華®獲批上市,將會為在中國台灣的RET變異的肺癌和甲狀腺癌患者帶來新的治療選擇。一直以來,基石藥業始終致力於研發創新藥物,滿足癌症患者未解決的醫療需求。未來,我們將繼續在腫瘤領域不斷探索,力爭加速為全球患者帶來更多高品質的藥物。”

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