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和黄医药

14.65

+0.35002.45%

成交量：1.23万

成交额：17.83万

市值：25.55亿

市盈率：5.63

高：14.65

开：14.32

低：14.32

收：14.30

52周最高：19.50

52周最低：11.51

股本：1.74亿

流通股本：1.04亿

量比：0.67

换手率：0.01%

股息：- -

股息率：- -

每股收益(TTM):2.60

每股收益(LYR):2.60

净资产收益率：45.25%

总资产收益率：-1.62%

市净率：2.06

市盈率(LYR):5.63

数据加载中...

总览公司新闻资讯公告

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和黄医药(00013)发布年度业绩股东应占溢利4.57亿美元同比增长1111.03%

下周备忘

财报前瞻｜和黄医药临床催化密集落地或优化营收结构，机构观点偏多

和黄医药(00013.HK)拟3月5日举行董事会会议批准年度业绩

零缺陷！和黄医药上海旗舰生产基地获美国食药管理部门认证

【券商聚焦】交银国际维持和黄医药(00013)买入评级指产品销售即将重新步入增长通道

更好满足患者需求！浦东创新药企持续发力

和黄医药涨逾5% SACHI III期研究结果于《柳叶刀》发表

Black Titan Corp盘中异动早盘股价大涨6.06%

和黄医药盘中异动早盘急速拉升5.23%报16.11美元

港股异动 | 和黄医药(00013)再涨超4% 月内累涨逾两成 SACHI III期研究结果于《柳叶刀》发表

和黄医药盘中涨超3% SACHI III期研究结果于《柳叶刀》发表

百时美施贵宝宣布评估玛伐凯泰治疗青少年有症状的梗阻性肥厚型心肌病（oHCM）的III 期临床试验SCOUT-HCM取得阳性结果

和黄医药(00013)宣布SACHI III期研究结果于《柳叶刀 (The Lancet)》发表

多重利好刺激股价走出“五连阳”，“躲过牛市”的和黄医药(00013)迎来反转时刻？

和黄医药盘中异动早盘快速拉升5.02%

索乐匹尼布取得突破性进展！和黄医药股价涨5.45%

和黄医药(00013)宣布索乐匹尼布用于治疗温抗体型自身免疫性溶血性贫血的 ESLIM-02中国研究的III期阶段取得阳性顶线结果

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09:43","pubTimestamp":1769391803,"startTime":"0","endTime":"0","summary":"该机构认为SAFFRON全球III期研究的成功概率较大。公司预计年中读出数据并提交NDA、2027年有望获批，该机构预计赛沃替尼全球销售峰值或超18亿美元。HMPL-A251已完成首个全球I期研究的首例患者给药，该机构建议重点关注其BD出海潜力。另两款ATTC候选分子将分别于1H26和2H26进入临床。","market":"nz","thumbnail":"https://static.szfiu.com/news/20250106/ZGNkM2E3NDVjMTk0N2Q5ZDk4NjYxNjc1YjA4NjMzOTA5MjkwMDE=.jpg","type":0,"news_type":0,"thumbnails":["https://static.szfiu.com/news/20250106/ZGNkM2E3NDVjMTk0N2Q5ZDk4NjYxNjc1YjA4NjMzOTA5MjkwMDE=.jpg"],"rights":null,"property":["rate"],"language":"zh","translate_title":"","themeId":null,"theme_name":"","theme_type":"","isJumpTheme":false,"source_url":"1973906","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":["HCM","00013"],"isVideo":false,"video":null,"gpt_icon":0},{"id":"2604679944","title":"更好满足患者需求！浦东创新药企持续发力","url":"https://stock-news.laohu8.com/highlight/detail?id=2604679944","media":"市场资讯","labels":[],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2604679944?lang=zh_cn&edition=fundamental","pubTime":"2026-01-17 00:00","pubTimestamp":1768579200,"startTime":"0","endTime":"0","summary":"eslim-01研究旨在评估索乐匹尼布长期治疗成人慢性原发itp患者的疗效和安全性。共有16例患者接受了imc002单次输注治疗，并全部纳入安全性分析。其中15例患者可评估疗效。据悉，基于本次研究结果，易慕峰生物已启动imc002在晚期gc/gej患者中的iii期随机对照临床研究，以进一步验证疗效和安全性。此次数据发布标志着易慕峰生物在实体瘤car-t领域，尤其是胃癌等高未满足临床需求适应症上的持续推进，为晚期胃/gej癌患者提供了新的治疗希望。","market":"us","thumbnail":null,"type":0,"news_type":0,"thumbnails":[],"rights":{"source":"tencent","url":"http://gu.qq.com/resources/shy/news/detail-v2/index.html#/?id=nesSN20260117004708a723b9e3&s=b","rn_cache_url":null,"customStyle":"body{padding-top:10px;}#news_title{font-weight:bold;#titleStyle#;}#news_description span{font-size:12px;#descriptionStyle#;}.footer-note{#statement#}","selectors":".mod-LoadTzbdNews, body","filters":".relate-stock, .hot-list, .recom-box, 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III期研究的结果于《柳叶刀》发表。SACHI是一项赛沃替尼和奥希替尼的联合疗法，用于治疗伴有MET扩增的接受一线表皮生长因子受体酪氨酸激酶抑制剂治疗后疾病进展的EGFR突变阳性局部晚期或转移性非小细胞肺癌患者的III期研究。基于SACHI研究的数据，赛沃替尼和奥希替尼的联合疗法已于2025年6月在中国获批。","market":"us","thumbnail":null,"type":0,"news_type":0,"thumbnails":[],"rights":{"source":"tencent","url":"http://gu.qq.com/resources/shy/news/detail-v2/index.html#/?id=nesSN20260116232631a72389bb&s=b","rn_cache_url":null,"customStyle":"body{padding-top:10px;}#news_title{font-weight:bold;#titleStyle#;}#news_description span{font-size:12px;#descriptionStyle#;}.footer-note{#statement#}","selectors":".mod-LoadTzbdNews, body","filters":".relate-stock, .hot-list, .recom-box, 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Corp股票出现异动，股价急速上涨6.06%。截至发稿，该股报1.75美元/股，成交量1.5502万股，换手率0.17%，振幅3.42%。Black Titan Corp股票所在的软件服务行业中，整体跌幅为0.41%。Black Titan Corp公司简介：Black Titan Corp 使用 PeopleSoft 平台提供人力资源和薪资咨询、软件实施和培训解决方案。","market":"us","thumbnail":null,"type":0,"news_type":0,"thumbnails":[],"rights":{"source":"tencent","url":"http://gu.qq.com/resources/shy/news/detail-v2/index.html#/?id=nesSN20260116225623a72374d6&s=b","rn_cache_url":null,"customStyle":"body{padding-top:10px;}#news_title{font-weight:bold;#titleStyle#;}#news_description span{font-size:12px;#descriptionStyle#;}.footer-note{#statement#}","selectors":".mod-LoadTzbdNews, body","filters":".relate-stock, .hot-list, .recom-box, 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III期研究的结果于《柳叶刀》发表。SACHI是一项赛沃替尼和奥希替尼的联合疗法，用于治疗伴有MET扩增的接受一线表皮生长因子受体酪氨酸激酶抑制剂治疗后疾病进展的EGFR突变阳性局部晚期或转移性非小细胞肺癌患者的III期研究。基于SACHI研究的数据，赛沃替尼和奥希替尼的联合疗法已于2025年6月在中国获批。","market":"fut","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/1393697.html","is_publish_highlight":false,"source_rank":0,"column":"","sentiment":"1","news_top_title":null,"news_tag":"dataReport","news_rank":0,"length":0,"strategy_id":0,"source":"stock_zhitongcaijing","symbols":["HCM","BK4585","BK1191","III","BK4588","BK1588","BK1587","BK4007","00013","BK4531","BK4134"],"isVideo":false,"video":null,"gpt_icon":0},{"id":"2603662471","title":"和黄医药盘中涨超3% SACHI III期研究结果于《柳叶刀》发表","url":"https://stock-news.laohu8.com/highlight/detail?id=2603662471","media":"新浪港股","labels":["dataReport"],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2603662471?lang=zh_cn&edition=fundamental","pubTime":"2026-01-15 10:40","pubTimestamp":1768444800,"startTime":"0","endTime":"0","summary":"　　和黄医药盘中涨超3%，截至发稿，股价上涨2.39%，现报23.98港元，成交额7741.10万港元。　　据和黄医药官微消息，1月14日，和黄医药宣布SACHI III期研究的结果于《柳叶刀 》发表。　　据介绍，赛沃替尼是一种强效、高选择性的口服MET TKI，由阿斯利康与和黄医药共同开发，并由阿斯利康商业化。基于SACHI研究的数据，赛沃替尼和奥希替尼的联合疗法已于2025年6月在中国获批。","market":"us","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":"https://finance.sina.com.cn/stock/hkstock/marketalerts/2026-01-15/doc-inhhiyxt4368442.shtml","is_publish_highlight":false,"source_rank":0,"column":"","sentiment":"1","news_top_title":null,"news_tag":"dataReport","news_rank":0,"length":0,"strategy_id":0,"source":"sina","symbols":["BK4007","BK4134","BK4585","BK4588","BK1191","BK4531","HCM","III","00013","BK1588","BK1587"],"isVideo":false,"video":null,"gpt_icon":0},{"id":"2603253613","title":"百时美施贵宝宣布评估玛伐凯泰治疗青少年有症状的梗阻性肥厚型心肌病（oHCM）的III 期临床试验SCOUT-HCM取得阳性结果","url":"https://stock-news.laohu8.com/highlight/detail?id=2603253613","media":"美通社","labels":["productRelease"],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2603253613?lang=zh_cn&edition=fundamental","pubTime":"2026-01-14 19:55","pubTimestamp":1768391700,"startTime":"0","endTime":"0","summary":"SCOUT-HCM 的阳性研究结果展现了玛伐凯泰有望成为首个用于青少年 oHCM 患者的心肌肌球蛋白抑制剂。青少年oHCM严重损害健康，主要临床表现与运动耐量下降相关。在欧盟，玛伐凯泰获批用于治疗有症状的NYHA心功能分级II-III级的梗阻性肥厚型心肌病成人患者。","market":"hk","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://wwwold.prnasia.com/story/archive/4863243_ZH63243_1","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":"prnasia","symbols":["BK4559","LU1261432733.SGD","LU1571399168.USD","LU1868836591.USD","LU0225771236.USD","LU0306806265.USD","BK4534","LU0237698245.USD","LU1093756325.SGD","IE0002141913.USD","BK4585","LU1430594728.SGD","IE00B2B36J28.USD","LU1074936037.SGD","LU1718418525.SGD","LU1868836914.USD","LU1291159041.SGD","LU0306807586.USD","IE0009355771.USD","BK4588","LU2125154935.USD","LU1093756168.USD","III","BK4134","LU0321505439.SGD","LU1323610961.USD","IE00BJJMRZ35.SGD","IE00BSNM7G36.USD","LU1868837136.USD","LU1670711123.USD","BMY","LU0985481810.HKD","LU0225284248.USD","IE00BJT1NW94.SGD","LU0114720955.EUR","HCM","IE00BFXG1179.USD","LU1989771016.USD","LU2242646821.SGD","LU0267386448.USD","LU0061475181.USD","LU0456855351.SGD","LU1670710588.SGD","LU1868837300.USD","LU2242652126.USD","LU1585245621.USD","LU0868494617.USD","LU1670710661.SGD","LU0096364046.USD","LU0321505868.SGD"],"isVideo":false,"video":null,"gpt_icon":0},{"id":"2603666888","title":"和黄医药(00013)宣布SACHI III期研究结果于《柳叶刀 (The Lancet)》发表","url":"https://stock-news.laohu8.com/highlight/detail?id=2603666888","media":"智通财经","labels":["dataReport"],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2603666888?lang=zh_cn&edition=fundamental","pubTime":"2026-01-14 12:11","pubTimestamp":1768363890,"startTime":"0","endTime":"0","summary":"智通财经APP讯，和黄医药 发布公告，公司今日宣布SACHI III期研究的结果于《柳叶刀 》发表。SACHI是一项赛沃替尼和奥希替尼的联合疗法用于治疗伴有MET扩增的接受一线表皮生长因子受体酪氨酸激酶抑制剂治疗后疾病进展的EGFR突变阳性局部晚期或转移性非小细胞肺癌患者的III期研究。基于SACHI研究的数据，赛沃替尼和奥希替尼的联合疗法已于2025年6月在中国获批。中国医学科学院肿瘤医院的王洁教授亦为SACHI 研究的联合主要研究者。","market":"hk","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/1392627.html","is_publish_highlight":false,"source_rank":0,"column":"","sentiment":"1","news_top_title":null,"news_tag":"dataReport","news_rank":0,"length":0,"strategy_id":0,"source":"stock_zhitongcaijing","symbols":["BK1588","BK1587","BK4531","BK1191","BK4134","BK4588","HCM","00013","BK4585","III","BK4007"],"isVideo":false,"video":null,"gpt_icon":0},{"id":"2602207113","title":"多重利好刺激股价走出“五连阳”，“躲过牛市”的和黄医药(00013)迎来反转时刻？","url":"https://stock-news.laohu8.com/highlight/detail?id=2602207113","media":"智通财经","labels":[],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2602207113?lang=zh_cn&edition=fundamental","pubTime":"2026-01-09 19:41","pubTimestamp":1767958896,"startTime":"0","endTime":"0","summary":"相较之下，作为一家手握3款商业化创新药并拥有首创抗体靶向偶联药物的创新药企，和黄医药却最终以8.56%的年度跌幅收场，显著跑输指数。去年8月7日美股盘前，和黄医药公布了其2025年中报业绩。最新数据显示，和黄医药的港股通持股比例已达27.28%。这便是和黄医药在25H2期内股价最大回撤幅度高达35.12%的重要原因之一。根据此前II期研究结果，索乐匹尼布针对wAIHA的整体应答率为66.7%，并展现出良好的安全性特征。","market":"fut","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/1391129.html","is_publish_highlight":false,"source_rank":0,"column":"","sentiment":"1","news_top_title":null,"news_tag":"","news_rank":0,"length":0,"strategy_id":0,"source":"stock_zhitongcaijing","symbols":["BK4007","00013","HCM","BK4585","BK4588","BK1191","BK4531","BK1588","BK1587"],"isVideo":false,"video":null,"gpt_icon":0},{"id":"2601480429","title":"和黄医药盘中异动 早盘快速拉升5.02%","url":"https://stock-news.laohu8.com/highlight/detail?id=2601480429","media":"市场透视","labels":[],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2601480429?lang=zh_cn&edition=fundamental","pubTime":"2026-01-07 22:46","pubTimestamp":1767797189,"startTime":"0","endTime":"0","summary":"北京时间2026年01月07日22时46分，和黄医药股票出现异动，股价急速上涨5.02%。截至发稿，该股报14.44美元/股，成交量7672股，换手率0.00%，振幅1.64%。和黄医药股票所在的制药行业中，整体涨幅为2.39%。和黄医药公司简介：和黄医药（中国）有限公司是一家生物制药公司，致力于发现、开发和商业化用于治疗癌症和免疫疾病的靶向疗法和免疫疗法。该公司目前在全球范围内拥有多个临床研究的癌症候选药物组合，并在其中国本土市场拥有广泛的商业基础设施。","market":"us","thumbnail":null,"type":0,"news_type":0,"thumbnails":[],"rights":{"source":"tencent","url":"http://gu.qq.com/resources/shy/news/detail-v2/index.html#/?id=nesSN2026010722462997a13368&s=b","rn_cache_url":null,"customStyle":"body{padding-top:10px;}#news_title{font-weight:bold;#titleStyle#;}#news_description span{font-size:12px;#descriptionStyle#;}.footer-note{#statement#}","selectors":".mod-LoadTzbdNews, body","filters":".relate-stock, 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20:04","pubTimestamp":1767787448,"startTime":"0","endTime":"0","summary":"另值得关注的是，除了温抗体型自身免疫性溶血性贫血以外，索乐匹尼布治疗免疫性血小板减少症的研究亦正在进行中。和黄医药透露，公司计划于2026年上半年重新提交索乐匹尼布，用于二线治疗免疫性血小板减少症的新药上市申请。综合来看，索乐匹尼布具有不错的商业化前景，后续若其在温抗体型自身免疫性溶血性贫血、免疫性血小板减少症两大适应症的新药上市申请获成功，将有望为公司业绩增长贡献助力。","market":"us","thumbnail":null,"type":0,"news_type":0,"thumbnails":[],"rights":{"source":"tencent","url":"http://gu.qq.com/resources/shy/news/detail-v2/index.html#/?id=nesSN20260107200638a6fead82&s=b","rn_cache_url":null,"customStyle":"body{padding-top:10px;}#news_title{font-weight:bold;#titleStyle#;}#news_description span{font-size:12px;#descriptionStyle#;}.footer-note{#statement#}","selectors":".mod-LoadTzbdNews, body","filters":".relate-stock, .hot-list, .recom-box, 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公布，新型脾酪氨酸激酶抑制剂索乐匹尼布用于治疗温抗体型自身免疫性溶血性贫血成人患者的ESLIM-02研究的III期注册阶段已达到第5至 24周治疗期间持久血红蛋白应答这一主要终点。ESLIM-02研究的完整数据将提交于近期的学术会议上发表。和黄医药计划于2026年上半年向中国国家药品监督管理局提交索乐匹尼布用于治疗温抗体型自身免疫性溶血性贫血的新药上市申请。","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/1389595.html","is_publish_highlight":false,"source_rank":0,"column":"","sentiment":"1","news_top_title":null,"news_tag":"dataReport","news_rank":0,"length":0,"strategy_id":0,"source":"stock_zhitongcaijing","symbols":["BK1588","BK1587","HCM","BK4588","BK4134","III","BK4007","BK1191","BK4585","BK4531","00013"],"isVideo":false,"video":null,"gpt_icon":0}],"pageSize":20,"totalPage":4,"pageCount":2,"totalSize":63,"code":"91000000","status":"200"}]}}