和黄医药(HCM)_个股概要_股票价格_最新资讯_行情走势_历史数据 - 老虎社区

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HCM 和黄医药

休市中 02-06 16:00:00 EST

15.18

+0.61

+4.19%

盘后15.18

+0.000.00%

16:10 EST

最高15.30	最低14.75	成交量3.50万
今开14.75	昨收14.57	日振幅3.81%
总市值26.48亿	流通市值15.79亿	总股本1.74亿
成交额52.69万	换手率0.03%	流通股本1.04亿
市净率--	ROE--	每股收益0.00
52周最高--	52周最低--	市盈率--
股息--	股息收益率--	ROA--

数据加载中...

北京优虎网络科技有限公司

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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":"sh","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":["00013","HCM"],"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://www.laohu8.com/m/news/2604679944?lang=zh_cn&edition=full","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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22:39","pubTimestamp":1768574365,"startTime":"0","endTime":"0","summary":"北京时间2026年01月16日22时39分，和黄医药股票出现异动，股价快速拉升5.23%。截至发稿，该股报16.11美元/股，成交量1.8325万股，换手率0.01%，振幅1.14%。和黄医药股票所在的制药行业中，整体跌幅为0.15%。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=nesSN2026011622392597a22348&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, .wx-sou","directOrigin":true},"property":[],"language":"zh","translate_title":"","themeId":null,"theme_name":"","theme_type":"","isJumpTheme":false,"source_url":"http://gu.qq.com/resources/shy/news/detail-v2/index.html#/?id=nesSN2026011622392597a22348&s=b","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":"tencent","symbols":["HCM","BK4585","BK4531","BK4007","BK4588"],"gpt_icon":0},{"id":"2603554869","title":"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","url":"https://stock-news.laohu8.com/highlight/detail?id=2603554869","media":"智通财经","labels":["dataReport"],"top":-1,"itemType":null,"share":"https://www.laohu8.com/m/news/2603554869?lang=zh_cn&edition=full","pubTime":"2026-01-16 11:03","pubTimestamp":1768532615,"startTime":"0","endTime":"0","summary":"智通财经APP获悉，和黄医药再涨超4%，月内累计涨幅超20%。消息面上，和黄医药宣布，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。","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":"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":["BK1588","BK4585","BK4531","00013","BK4007","BK4588","III","HCM","BK1191","BK4134","BK1587"],"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://www.laohu8.com/m/news/2603662471?lang=zh_cn&edition=full","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":"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":"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":["BK4588","HCM","00013","BK1587","III","BK4585","BK4531","BK1588","BK4007","BK1191","BK4134"],"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://www.laohu8.com/m/news/2603253613?lang=zh_cn&edition=full","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":"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":"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":["IE00BSNM7G36.USD","LU1868837300.USD","IE0002141913.USD","LU0868494617.USD","IE00BFXG1179.USD","III","LU0225771236.USD","LU0267386448.USD","LU2242646821.SGD","LU1430594728.SGD","LU0306807586.USD","LU0985481810.HKD","LU1291159041.SGD","BK4585","BK4534","HCM","LU0096364046.USD","LU0456855351.SGD","LU0114720955.EUR","IE0009355771.USD","LU0225284248.USD","LU0321505868.SGD","LU1074936037.SGD","LU2125154935.USD","BMY","LU1585245621.USD","LU1670710588.SGD","IE00B2B36J28.USD","LU0237698245.USD","BK4134","LU1868837136.USD","LU1571399168.USD","LU1323610961.USD","IE00BJJMRZ35.SGD","BK4559","LU1868836591.USD","LU0061475181.USD","LU1093756168.USD","IE00BJT1NW94.SGD","LU1868836914.USD","LU0306806265.USD","LU1093756325.SGD","LU1670710661.SGD","BK4588","LU0321505439.SGD","LU1261432733.SGD","LU1670711123.USD","LU1718418525.SGD","LU1989771016.USD","LU2242652126.USD"],"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://www.laohu8.com/m/news/2603666888?lang=zh_cn&edition=full","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":["BK1587","BK1191","BK4134","BK1588","BK4531","00013","BK4585","BK4007","HCM","III","BK4588"],"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://www.laohu8.com/m/news/2602207113?lang=zh_cn&edition=full","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":"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/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":["BK4531","BK1587","BK1588","BK4007","HCM","BK4588","00013","BK1191","BK4585"],"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://www.laohu8.com/m/news/2601480429?lang=zh_cn&edition=full","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, .hot-list, 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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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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":"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/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":["BK1587","BK1191","BK4134","BK1588","BK4531","00013","BK4585","BK4007","HCM","III","BK4588"],"gpt_icon":0},{"id":"2601078362","title":"和黄医药(00013)启动现正进行中的索凡替尼联合卡瑞利珠单抗用于治疗初治胰腺导管腺癌研究的III期阶段","url":"https://stock-news.laohu8.com/highlight/detail?id=2601078362","media":"智通财经","labels":["dataReport"],"top":-1,"itemType":null,"share":"https://www.laohu8.com/m/news/2601078362?lang=zh_cn&edition=full","pubTime":"2026-01-05 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公布，赛沃替尼用于经过至少2种治疗后失败的MET基因扩增的局部晚期或转移性胃癌或胃食道连接部腺癌成人患者的新药上市申请已获中国国家药品监督管理局受理，并获纳入优先审评。该新药上市申请是基于一项在中国开展的赛沃替尼用于治疗伴有MET扩增的胃癌患者的单臂、多中心、开放标签的II期注册研究的数据。","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/1387177.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_zhitongcaijing","symbols":["HCM","MET","BK4007","BK4531","BK4585","BK4588","LU1496350502.SGD","LU1291159041.SGD","LU1989772840.SGD","BK1587","LU1989772923.USD","LU1989771016.USD","BK1588","00013","BK4162","BK1191"],"gpt_icon":0},{"id":"2595788714","title":"和黄医药(00013)宣布凡瑞格拉替尼 (HMPL-453) 用于二线治疗肝内胆管癌的中国新药上市申请获受理并获纳入优先审评","url":"https://stock-news.laohu8.com/highlight/detail?id=2595788714","media":"智通财经","labels":["productRelease"],"top":-1,"itemType":null,"share":"https://www.laohu8.com/m/news/2595788714?lang=zh_cn&edition=full","pubTime":"2025-12-29 16:36","pubTimestamp":1766997386,"startTime":"0","endTime":"0","summary":"智通财经APP讯，和黄医药 发布公告，凡瑞格拉替尼 用于既往接受过系统性治疗，且具有成纤维细胞生长因子受体2融合或重排的晚期、转移性或不可手术切除的肝内胆管癌成人患者的新药上市申请已获中国国家药品监督管理局受理 ，并获纳入优先审评。凡瑞格拉替尼是一种新型、选择性的FGFR1 、2和3口服抑制剂。近年来，肝内胆管癌发病率呈持续上升趋势，5年总生存率约9%。","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":"http://www.zhitongcaijing.com/content/detail/1386500.html","is_publish_highlight":false,"source_rank":0,"column":"","sentiment":"1","news_top_title":"和黄医药(00013)宣布凡瑞格拉替尼 (HMPL-453) 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