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中國生物製藥

5.505

+0.0851.57%

成交量：2,859.10萬

成交額：1.58億

市值：1,028.50億

市盈率：36.28

高：5.585

開：5.500

低：5.395

收：5.420

52周最高：8.598

52周最低：4.136

股本：186.83億

香港流通股本：186.83億

量比：0.95

換手率：0.15%

股息：0.12

股息率：2.23%

每股收益(LYR):0.152

淨資產收益率：14.07%

總資產收益率：7.51%

市淨率：2.70

市盈率(LYR):36.28

市銷率: 2.61

資料載入中...

總覽公司新聞資訊公告

中國生物製藥(01177.HK)貝莫蘇拜單抗聯合安羅替尼新適應症獲批上市

阿斯达克财经

中國生物製藥：附屬公司自研1類創新藥貝莫蘇拜單抗注射液聯合療法獲批上市

中國生物製藥(01177.HK)：貝莫蘇拜單抗聯合化療序貫聯合安羅替尼一線治療鱗狀非小細胞肺癌新適應症獲批上市

中國生物製藥：NMPA批准貝莫蘇拜單抗聯合化療序貫安羅替尼一線治療肺鱗癌

異動解讀｜中國生物製藥盤中上漲3.25%，多款新藥密集獲批推進

中生製藥(01177.HK)第二代氟比洛芬貼劑獲批上市

阿斯达克财经

中國生物製藥(01177)宣佈第二代氟比洛芬貼劑獲NMPA批准上市

中國生物製藥(01177.HK)：第二代氟比洛芬貼劑獲批上市

中國生物製藥(01177)將於2026年8月19日召開董事會審議中期業績及派息事宜

港股早盤震盪走弱恒生指數半日跌1.75% 友邦保險（01299）跌8.75%

中國生物製藥（01177）BCL-2抑制劑TQB3909遞交NDA並獲CDE受理

中生製藥(01177.HK)TQB3909片新藥上市申請獲受理

阿斯达克财经

中國生物製藥(01177.HK)：TQB3909片(BCL-2 抑制劑)新藥上市申請獲得受理

中國生物製藥：創新藥TQB2102獲第三項突破性療法認定

中國生物製藥（01177）ADC新藥TQB2102第三次入選CDE突破性治療名單

中國生物製藥(01177)：TQB2102「HER2雙抗ADC」第三次被CDE納入突破性治療藥物名單

中國生物製藥TQB2102 HER2雙特異性ADC獲CDE突破性療法認定，針對HER2低表達乳腺癌

中國生物製藥2026年7月股份變動月報：已發行股份減少22,065,000股

中國生物製藥(01177)出現大手賣出220萬股，成交價$4.9，涉資1.078千萬

阿斯达克财经

中國生物製藥（01177）將於2026年CSCO年會發布21項研究成果含5項口頭報告

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20:32","pubTimestamp":1786105920,"startTime":"0","endTime":"0","summary":"8月7日，中国生物制药（01177）发布公告，附属公司正大天晴药业集团股份有限公司自主研发的国家1类创新药贝莫苏拜单抗注射液联合化疗序贯联合盐酸安罗替尼胶囊已获得中国国家药品监督管理局的上市批准，用于一线治疗局部晚期或转移性鳞状非小细胞肺癌。公告提到，这是安罗替尼获批的第12个适应症，是贝莫苏拜单抗获批的第6个适应症。","market":"hk","thumbnail":null,"type":0,"news_type":0,"thumbnails":[],"rights":{"source":"stock_eastmoney","url":"http://finance.eastmoney.com/a/202608073835411830.html","rn_cache_url":null,"directOrigin":true},"property":[],"language":"zh","translate_title":"","themeId":null,"theme_name":"","theme_type":"","isJumpTheme":false,"source_url":"http://finance.eastmoney.com/a/202608073835411830.html","is_publish_highlight":false,"source_rank":0,"column":"","sentiment":"1","news_top_title":null,"news_tag":"productRelease","news_rank":0,"length":0,"strategy_id":0,"source":"stock_eastmoney","symbols":["BK1589","159992","BK1515","IE00BZ08YS42.EUR","BK1161","IBBQ","01177","BK1191","06978","BK1574","HK0000165453.HKD","IE00BZ08YR35.GBP","MEDX","IE00BZ08YT58.USD","IPOS","BK1521","LNGR"],"isVideo":false,"video":null,"gpt_icon":0},{"id":"2657610364","title":"中國生物製藥(01177.HK)：貝莫蘇拜單抗聯合化療序貫聯合安羅替尼一線治療鱗狀非小細胞肺癌新適應症獲批上市","url":"https://stock-news.laohu8.com/highlight/detail?id=2657610364","media":"智通财经","labels":[],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2657610364?lang=zh_tw&edition=fundamental","pubTime":"2026-08-07 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18:59","pubTimestamp":1786100349,"startTime":"0","endTime":"0","summary":"中国生物制药宣布，国家药监局（NMPA）已正式批准贝莫苏拜单抗联合化疗，随后序贯安罗替尼的方案，用于一线治疗鳞状非小细胞肺癌（Sq-NSCLC）。这一突破性进展，为晚期肺鳞癌患者带来了全新的治疗选择。","market":"us","thumbnail":"","type":0,"news_type":0,"thumbnails":[],"rights":null,"property":[],"language":"zh","translate_title":"","themeId":null,"theme_name":"","theme_type":"","isJumpTheme":false,"source_url":"","is_publish_highlight":false,"source_rank":0,"column":"","sentiment":"1","news_top_title":null,"news_tag":"productRelease","news_rank":0,"length":0,"strategy_id":0,"source":null,"symbols":["BK1191","BK1521","BK1589","IE00BZ08YT58.USD","BK1515","HK0000165453.HKD","IE00BZ08YR35.GBP","IE00BZ08YS42.EUR","01177"],"isVideo":false,"video":null,"gpt_icon":0},{"id":"1122425877","title":"異動解讀｜中國生物製藥盤中上漲3.25%，多款新藥密集獲批推進","url":"https://stock-news.laohu8.com/highlight/detail?id=1122425877","media":"行情直击","labels":[],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/1122425877?lang=zh_tw&edition=fundamental","pubTime":"2026-08-07 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17:24","pubTimestamp":1786008240,"startTime":"0","endTime":"0","summary":"中生制药(01177.HK) 公布，附属北京泰德的国家5.1类新药第二代氟比洛芬贴剂，商品名为泽普思，已获得国家药品监督管理局(NMPA)批准上市，用于镇痛、消炎：骨关节炎、肩周炎、肌腱及腱鞘炎、腱鞘周围炎、肱骨外上髁炎(网球肘)、肌肉痛、外伤所致肿胀、疼痛。该产品亦获得NMPA 4年数据保护期。(ha/u)(港股报价延迟最少十五分钟。沽空资料截至 2026-08-06 16:25。)AASTOCKS新闻","market":"hk","thumbnail":"https://plib.aastocks.com/aafnnews/image/medialib/20220728114525438_s.jpg","type":0,"news_type":0,"thumbnails":["https://plib.aastocks.com/aafnnews/image/medialib/20220728114525438_s.jpg"],"rights":{"source":"aastocks_highlight","url":"http://www.aastocks.com/tc/stocks/news/aafn-con/NOW.1536995/latest-news/AAFN","rn_cache_url":null,"directOrigin":true},"property":[],"language":"zh","translate_title":"","themeId":null,"theme_name":"","theme_type":"","isJumpTheme":false,"source_url":"http://www.aastocks.com/tc/stocks/news/aafn-con/NOW.1536995/latest-news/AAFN","is_publish_highlight":false,"source_rank":0,"column":"","sentiment":"1","news_top_title":null,"news_tag":"productRelease","news_rank":0,"length":0,"strategy_id":0,"source":"aastocks_highlight","symbols":["IE00BZ08YS42.EUR","HK0000165453.HKD","01477","BK1521","01177","BK1589","BK1574","IE00BZ08YT58.USD","BK1515","BK1191","IE00BZ08YR35.GBP"],"isVideo":false,"video":null,"gpt_icon":0},{"id":"1110598101","title":"中國生物製藥(01177)宣佈第二代氟比洛芬貼劑獲NMPA批准上市","url":"https://stock-news.laohu8.com/highlight/detail?id=1110598101","media":"公告速递","labels":["productRelease","SGX"],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/1110598101?lang=zh_tw&edition=fundamental","pubTime":"2026-08-06 17:21","pubTimestamp":1786008111,"startTime":"0","endTime":"0","summary":"2026年8月6日，中国生物制药有限公司发布自愿公告称，其附属公司北京泰德制药股份有限公司的国家5.1类新药第二代氟比洛芬贴剂已获中国国家药品监督管理局批准上市。公告指出，中国慢性疼痛患者超过2亿，且呈现年轻化趋势。中国生物制药已建立现代透皮技术平台及产品矩阵。","market":"sh","thumbnail":"","type":0,"news_type":0,"thumbnails":[],"rights":null,"property":[],"language":"zh","translate_title":"","themeId":null,"theme_name":"","theme_type":"","isJumpTheme":false,"source_url":"","is_publish_highlight":false,"source_rank":0,"column":"","sentiment":"1","news_top_title":null,"news_tag":"productRelease,SGX","news_rank":0,"length":0,"strategy_id":0,"source":null,"symbols":["01177"],"isVideo":false,"video":null,"gpt_icon":0},{"id":"2657689222","title":"中國生物製藥(01177.HK)：第二代氟比洛芬貼劑獲批上市","url":"https://stock-news.laohu8.com/highlight/detail?id=2657689222","media":"智通财经","labels":[],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2657689222?lang=zh_tw&edition=fundamental","pubTime":"2026-08-06 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后，获得的第三项突破性治疗认定。","market":"hk","thumbnail":"","type":0,"news_type":0,"thumbnails":[],"rights":null,"property":[],"language":"zh","translate_title":"","themeId":null,"theme_name":"","theme_type":"","isJumpTheme":false,"source_url":"","is_publish_highlight":false,"source_rank":0,"column":"","sentiment":"1","news_top_title":null,"news_tag":"productRelease,SGX","news_rank":0,"length":0,"strategy_id":0,"source":null,"symbols":["01177"],"isVideo":false,"video":null,"gpt_icon":0},{"id":"2656248463","title":"中國生物製藥(01177)：TQB2102「HER2雙抗ADC」第三次被CDE納入突破性治療藥物名單","url":"https://stock-news.laohu8.com/highlight/detail?id=2656248463","media":"智通财经","labels":["corporation"],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2656248463?lang=zh_tw&edition=fundamental","pubTime":"2026-08-03 16:37","pubTimestamp":1785746238,"startTime":"0","endTime":"0","summary":"智通财经APP讯，中国生物制药 发布公告，集团附属公司正大天晴药业集团股份有限公司自主研发的国家1类创新药TQB2102“HER2双抗 ADC”已被中国国家药品监督管理局药品审评中心纳入突破性治疗药物名单，用于在复发或转移性疾病阶段未接受过化疗的不可切除或转移性HER2低表达成人乳腺癌患者。这是继HER2阳性早期乳腺癌新辅助治疗、HER2 IHC 3+晚期结直肠癌之后，TQB2102获得的第三项突破性疗法认定，进一步印证了其在HER2表达实体瘤治疗领域的广泛应用潜力。","market":"sh","thumbnail":null,"type":0,"news_type":0,"thumbnails":[],"rights":null,"property":[],"language":"zh","translate_title":"","themeId":null,"theme_name":"","theme_type":"","isJumpTheme":false,"source_url":"http://www.zhitongcaijing.com/content/detail/1475261.html","is_publish_highlight":false,"source_rank":0,"column":"","sentiment":"1","news_top_title":null,"news_tag":"corporation","news_rank":0,"length":0,"strategy_id":0,"source":"stock_zhitongcaijing","symbols":["SGDM","ADC","BK1515","01177","IE00BZ08YS42.EUR","IE00BZ08YT58.USD","NETL","XME","BK1191","CDE","BK4080","LU1223082196.USD","SIL","BK1589","BK1521","HK0000165453.HKD","LU1223083913.SGD","BK4017","GDXJ","LU1223082519.USD","IE00BZ08YR35.GBP","BK4231"],"isVideo":false,"video":null,"gpt_icon":0},{"id":"1182089708","title":"中國生物製藥TQB2102 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