
台灣成亞洲第一個核准雅絲媞®用於子宮內膜異位症市場,擴大婦女健康領域布局
健喬信元與日本橘生藥品共同宣布,口服GnRH拮抗劑「雅絲媞®膜衣錠 100 毫克」獲衛福部核准新增子宮內膜異位症適應症。台灣成亞洲首個核准市場,為育齡女性提供全新口服治療選擇。
AI-generated summary
橘生藥品於2022年11月授予健喬信元Yselty®在台開發及銷售權利,原核准適應症為治療子宮肌瘤引起的經血過多。
健喬董事長林智暉。
〔記者陳永吉/台北報導〕國內藥廠健喬信元(4114)與日本合作夥伴橘生藥品(Kissei)今日共同宣布,新一代口服促性腺激素釋放激素(GnRH)拮抗劑「雅絲媞(Yselty)®膜衣錠 100 毫克」獲衛生福利部核准新增子宮內膜異位症適應症,適用於治療曾接受內科或外科治療的成年育齡女性因子宮內膜異位症引起的疼痛症狀。健喬表示,台灣是亞洲第一個核准雅絲媞®用於子宮內膜異位症的市場,為國內患者帶來全新的口服治療新選擇。
健喬表示,橘生藥品於2022年11月授予健喬信元Yselty®在台開發及銷售權利,2025年10月取得台灣上市許可,原核准適應症為治療成年育齡女性因子宮肌瘤引起的經血過多,同年12月提出新增子宮內膜異位症適應症申請,2026年3月以子宮肌瘤適應症在台上市,目前已獲174家醫療院所引進,涵蓋12家醫學中心,此次新增適應症獲准,進一步擴大健喬在婦女健康領域的治療布局。
健喬指出,子宮內膜異位症是育齡女性常見的慢性婦科疾病,患者可能出現痛經、骨盆腔疼痛及性交疼痛,部分患者也可能面臨不孕。此次新增適應症,為曾接受內科或外科治療、仍受疼痛困擾的患者提供另一項口服治療選擇。
AI outlook — possibilities, not facts
雅絲媞®將在台推展子宮內膜異位症適應症治療應用
Very likely · Within months

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