美股詳情

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和黃醫藥

14.96

+0.07000.47%

成交量：3.99萬

成交額：59.51萬

市值：26.10億

市盈率：5.65

高：15.08

開：14.84

低：14.71

收：14.89

52周最高：19.50

52周最低：11.51

股本：1.74億

流通股本：1.04億

量比：1.05

換手率：0.04%

股息：- -

股息率：- -

每股收益(TTM):2.65

每股收益(LYR):0.2000

淨資產收益率：46.90%

總資產收益率：-0.81%

市淨率：2.12

市盈率(LYR):74.80

資料載入中...

總覽公司新聞資訊公告

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Black Titan Corp盤中異動早盤股價大漲6.06%

和黃醫藥盤中異動早盤急速拉升5.23%報16.11美元

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和黃醫藥盤中升逾3% SACHI III期研究結果於《柳葉刀》發表

百時美施貴寶宣佈評估瑪伐凱泰治療青少年有症狀的梗阻性肥厚型心肌病（oHCM）的III 期臨牀試驗SCOUT-HCM取得陽性結果

和黃醫藥(00013)宣佈SACHI III期研究結果於《柳葉刀 (The Lancet)》發表

多重利好刺激股價走出「五連陽」，「躲過牛市」的和黃醫藥(00013)迎來反轉時刻？

和黃醫藥盤中異動早盤快速拉升5.02%

索樂匹尼布取得突破性進展！和黃醫藥股價漲5.45%

和黃醫藥(00013)宣佈索樂匹尼布用於治療温抗體型自身免疫性溶血性貧血的 ESLIM-02中國研究的III期階段取得陽性頂線結果

和黃醫藥(00013)啓動現正進行中的索凡替尼聯合卡瑞利珠單抗用於治療初治胰腺導管腺癌研究的III期階段

和黃醫藥(00013)宣佈賽沃替尼 (savolitinib) 用於治療伴有MET擴增的胃癌患者的中國新藥上市申請獲受理並獲納入優先審評

和黃醫藥(00013)宣佈凡瑞格拉替尼 (HMPL-453) 用於二線治療肝內膽管癌的中國新藥上市申請獲受理並獲納入優先審評

國家藥監局批准阿夫凱泰片上市

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中国网财经

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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, 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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":"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/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","BK1587","BK4531","BK4588","BK4585","BK1191","BK4134","BK1588","III","00013","BK4007"],"gpt_icon":0},{"id":"2603662471","title":"和黃醫藥盤中升逾3% SACHI III期研究結果於《柳葉刀》發表","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_tw&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":"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":["BK1588","00013","HCM","III","BK4007","BK4531","BK4134","BK4585","BK1587","BK4588","BK1191"],"gpt_icon":0},{"id":"2603253613","title":"百時美施貴寶宣佈評估瑪伐凱泰治療青少年有症狀的梗阻性肥厚型心肌病（oHCM）的III 期臨牀試驗SCOUT-HCM取得陽性結果","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_tw&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":["LU1868836591.USD","LU0225771236.USD","LU1718418525.SGD","LU2242646821.SGD","LU0306807586.USD","LU1670710588.SGD","LU1670711123.USD","IE0002141913.USD","BK4134","IE00B2B36J28.USD","LU2125154935.USD","LU0114720955.EUR","LU1868837300.USD","LU1261432733.SGD","BK4585","LU0267386448.USD","IE00BJJMRZ35.SGD","IE00BFXG1179.USD","IE00BSNM7G36.USD","LU0225284248.USD","IE0009355771.USD","LU0061475181.USD","LU0456855351.SGD","IE00BJT1NW94.SGD","LU0306806265.USD","III","LU1430594728.SGD","BK4534","BK4559","LU1074936037.SGD","LU0321505868.SGD","LU1323610961.USD","LU1868836914.USD","LU1670710661.SGD","LU2242652126.USD","LU0237698245.USD","LU0321505439.SGD","LU1291159041.SGD","LU1868837136.USD","LU0096364046.USD","BMY","BK4588","LU0985481810.HKD","LU1571399168.USD","LU1989771016.USD","LU1093756168.USD","LU1585245621.USD","LU1093756325.SGD","LU0868494617.USD","HCM"],"gpt_icon":0},{"id":"2603666888","title":"和黃醫藥(00013)宣佈SACHI III期研究結果於《柳葉刀 (The Lancet)》發表","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_tw&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":["BK4588","HCM","00013","BK1587","III","BK4585","BK4531","BK1588","BK4007","BK1191","BK4134"],"gpt_icon":0},{"id":"2602207113","title":"多重利好刺激股價走出「五連陽」，「躲過牛市」的和黃醫藥(00013)迎來反轉時刻？","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_tw&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":"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/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":["BK1588","00013","BK1587","HCM","BK4585","BK4588","BK1191","BK4531","BK4007"],"gpt_icon":0},{"id":"2601480429","title":"和黃醫藥盤中異動 早盤快速拉升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_tw&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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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":"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/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","BK4531","BK4588","HCM","BK4585","BK4134","III","00013","BK1191","BK4007","BK1587"],"gpt_icon":0},{"id":"2601078362","title":"和黃醫藥(00013)啓動現正進行中的索凡替尼聯合卡瑞利珠單抗用於治療初治胰腺導管腺癌研究的III期階段","url":"https://stock-news.laohu8.com/highlight/detail?id=2601078362","media":"智通财经","labels":["dataReport"],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2601078362?lang=zh_tw&edition=fundamental","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":"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/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","BK4585","LU1989772840.SGD","LU1989772923.USD","BK4162","00013","BK4588","BK1587","BK1588","LU1989771016.USD","MET","BK4007","LU1291159041.SGD","BK1191","BK4531","LU1496350502.SGD"],"gpt_icon":0},{"id":"2595788714","title":"和黃醫藥(00013)宣佈凡瑞格拉替尼 (HMPL-453) 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12月22日，近日，国家药品监督管理局通过优先审评审批程序，批准Cytokinetics,Incorporated申报的1类创新药阿夫凯泰片(商品名：星舒平)上市，该药用于治疗纽约心脏协会(NYHA)心功能分级II-III级的梗阻性肥厚型心肌病(HCM)成人患者，以改善运动能力和症状。该药品上市为患者提供了新的治疗选择。","market":"hk","thumbnail":"https://media.bjnews.com.cn/cover/2025/12/04/5660775925944492210.jpeg?x-oss-process=image/resize,m_lfit,w_365","type":0,"news_type":0,"thumbnails":["https://media.bjnews.com.cn/cover/2025/12/04/5660775925944492210.jpeg?x-oss-process=image/resize,m_lfit,w_365"],"rights":{"source":"highlight_bjnews","url":"https://www.bjnews.com.cn/detail/1766388465129356.html","rn_cache_url":null,"customStyle":"handleCustomStyle(customStyle, ThemeStyle, getFont(fontSize))","selectors":"#main .nleft","filters":".ntit, 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