【瞩目】石药集团吸入剂大爆发，超200亿市场再掀波澜

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精彩内容3月5日，石药集团发布公告，集团开发的茚达特罗莫米松吸入粉雾剂获批在中国开展临床试验。米内网数据显示，吸入剂（化+中+生）在近年中国三大终端六大市场均保持200亿元以上销售规模，2025年Q1-Q3同比略有下滑，呼吸系统用药（化+生）是TOP1大类。3月6日，集团开发的化药1类新药SYH2059吸入粉雾剂获美国FDA批准，可以在美国开展临床试验。茚达特罗莫米松吸入粉雾剂用于成人和12岁及...

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Waves Again","themeId":null,"isJumpTheme":false,"ttsUrl":null,"symbols_score_info":{"01093":1.5},"content_text":"精彩内容3月5日，石药集团发布公告，集团开发的茚达特罗莫米松吸入粉雾剂获批在中国开展临床试验。米内网数据显示，吸入剂（化+中+生）在近年中国三大终端六大市场均保持200亿元以上销售规模，2025年Q1-Q3同比略有下滑，呼吸系统用药（化+生）是TOP1大类。3月6日，集团开发的化药1类新药SYH2059吸入粉雾剂获美国FDA批准，可以在美国开展临床试验。茚达特罗莫米松吸入粉雾剂用于成人和12岁及以上青少年哮喘的维持治疗。该产品是首个纳入《国家医保目录（2022年版）》中可一天一次使用的吸入ICS-LABA二联复方吸入制剂，为哮喘患者提供更高效、更便捷的治疗选择。2025年Q1-Q3中国三大终端六大市场吸入剂（化+中+生）大类格局来源：米内网格局数据库吸入剂（化+中+生）在近年中国三大终端六大市场（统计范围见文末）均保持200亿元以上销售规模，2025年Q1-Q3同比略有下滑，呼吸系统用药（化+生）是TOP1大类。米内网数据显示，茚达特罗莫米松吸入粉雾剂仅Grand Medical拥有生产批文，暂无企业报产在审。石药集团表示，此次茚达特罗莫米松吸入粉雾剂获批临床，是集团高端创新吸入技术平台的又一重要成果，为管线内后续吸入制剂的开发奠定良好基础。3月6日，石药集团再发公告，集团开发的化药1类新药SYH2059吸入粉雾剂获美国FDA批准，可以在美国开展临床试验。该产品是集团1款全新的、具有完全自主知识产权的高活性与高选择性磷酸二酯酶4B(PDE4B)抑制剂，获批的临床适应症为肺纤维化（PF），包括特发性肺纤维化（IPF）及进展性肺纤维化（PPF）。目前市场上用于治疗该类疾病的药物为数不多，且患者治疗获益有限，该产品具有望成为该类疾病的有效治疗药物，具有较大的临床开发价值。在此之前，石药集团新品公告捷报频传。艾美赛珠单抗注射液（SYS6053）在中国获批临床，该产品为原研药（商品名：舒友立乐）的生物类似药，适用于A型血友病患者；注射用紫杉醇白蛋白纳米粒（速溶型）（SYHX2011G1）已获美国FDA批准，可以在美国开展临床试验，该产品采用专利技术开发的新型纳米制剂，有望成为全球首个速溶白蛋白结合型紫杉醇制剂。资料来源：公司公告、米内网数据库注：米内网《中国三大终端六大市场药品竞争格局》，统计范围：城市公立医院和县级公立医院、城市社区中心和乡镇卫生院、城市实体药店和网上药店，不含民营医院、私人诊所、村卫生室，不含县乡村药店；上述销售额以产品在终端的平均零售价计算。如有疏漏，欢迎指正！","kind":"news","is_publish_news":true,"is_publish_highlight":false,"is_publish_live":false,"is_publish_wemedia":null,"editions":null,"column":"","sentiment":"2","news_tag":"productRelease","news_rank":0,"isVideo":false,"video":null,"symbols":[],"gpt_button":1,"need_auth":false,"need_login_tip":false,"code":"91000000","status":"200"},"commentList":[],"isCommentEnd":true,"newsSizeData":{"likeSize":0,"commentSize":0,"repostSize":0,"favoriteSize":0,"likeStatus":false,"favoriteStatus":false},"APP":{"userAgent":"Mozilla/5.0 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