美股详情

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4.12

-0.1400-3.29%

盘后：4.120.00000.00%19:34 EDT

成交量：16.93万

成交额：69.72万

市值：1.97亿

市盈率：19.62

高：4.26

开：4.26

低：4.06

收：4.26

52周最高：6.45

52周最低：3.74

股本：4,788.41万

流通股本：3,498.93万

量比：0.88

换手率：0.48%

股息：0.18

股息率：4.37%

每股收益(TTM):0.2100

每股收益(LYR):0.1900

净资产收益率：11.17%

总资产收益率：5.99%

市净率：2.09

市盈率(LYR):21.68

数据加载中...

总览公司新闻公告

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10:10","pubTimestamp":1774318245,"startTime":"0","endTime":"0","summary":"消息面上，四环医药发布公告，公司旗下非全资附属公司轩竹生物科技股份有限公司的创新药安奈拉唑钠肠溶片用于治疗成人反流性食管炎的中国III期临床试验已顺利完成全部500名受试者入组。据悉，安奈拉唑钠肠溶片于2023年6月获得中国国家药品监督管理局批准上市，用于患者治疗十二指肠溃疡。此次III期临床研究于2025年7月全面展开，近期完成受试者入组，标志着本公司在创新药物研发方面取得了重要进展。","market":"nz","thumbnail":"https://static.szfiu.com/news/20241108/YjNiOTNjODIxNjM4MTUzMTI5MQ==.jpg","type":0,"news_type":0,"thumbnails":["https://static.szfiu.com/news/20241108/YjNiOTNjODIxNjM4MTUzMTI5MQ==.jpg"],"rights":null,"property":[],"language":"zh","translate_title":"","themeId":null,"theme_name":"","theme_type":"","isJumpTheme":false,"source_url":"1977089","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":null,"symbols":["BK1191","BK4134","III","BK1593","00460","BK1600","02575","BK1515"],"isVideo":false,"video":null,"gpt_icon":0},{"id":"2621337490","title":"康宁杰瑞制药-B(09966)：KN026辅助治疗HER2+乳腺癌III期临床研究完成首例患者给药","url":"https://stock-news.laohu8.com/highlight/detail?id=2621337490","media":"智通财经","labels":["productRelease"],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2621337490?lang=zh_cn&edition=fundamental","pubTime":"2026-03-24 08:07","pubTimestamp":1774310843,"startTime":"0","endTime":"0","summary":"双靶向联合化疗辅助治疗HER2+ BC 对比仅含曲妥珠单抗的方案，可进一步降低复发风险，其中淋巴结阳性人群的获益最为显著。KN026-007是一项随机、对照、开放、多中心III期临床研究，预计纳入约1,800例术后组织学确认区域淋巴结阳性数量≥4个的可切除HER2+ BC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://www.zhitongcaijing.com/content/detail/1417758.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":["BK1574","BK1161","BK4134","09966","III"],"isVideo":false,"video":null,"gpt_icon":0},{"id":"2621672560","title":"华莱士成立信息服务公司，注册资本5000万","url":"https://stock-news.laohu8.com/highlight/detail?id=2621672560","media":"经济观察网","labels":[],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2621672560?lang=zh_cn&edition=fundamental","pubTime":"2026-03-23 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B细胞淋巴瘤患者的注册性III期临床试验。该研究是一项随机、双盲、阳性对照的III期临床研究，旨在评估HMPL-760联合R-GemOx方案对比安慰剂联合RGemOx方案用于治疗既往接受过一线系统化疗、免疫治疗或免疫化疗联合治疗后复发或难治性且不适合移植的弥漫性大B细胞淋巴瘤患者的疗效、安全性和药代动力学。","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/1417131.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":["BK4588","BK1191","BK4134","00013","BK4007","III","HCM","BK1587","BK4531","BK1588","BK4585"],"isVideo":false,"video":null,"gpt_icon":0},{"id":"2621742594","title":"宜明昂科-B(01541)成功完成IMM01(替达派西普)用于慢性粒-单核细胞白血病(CMML)一线治疗的III期临床试验中期分析的133例患者招募","url":"https://stock-news.laohu8.com/highlight/detail?id=2621742594","media":"智通财经","labels":["dataReport"],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2621742594?lang=zh_cn&edition=fundamental","pubTime":"2026-03-23 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18:34","pubTimestamp":1774175640,"startTime":"0","endTime":"0","summary":"3月22日，四环医药（00460）发布公告，本公司旗下非全资附属公司轩竹生物科技股份有限公司的创新药安奈拉唑钠肠溶片（商品名：安久卫?）用于治疗成人反流性食管炎的中国III期临床试验已顺利完成全部500名受试者入组。该试验是一项多中心、随机、双盲双模拟、阳性药物平行对照的关键性研究，旨在评估安奈拉唑钠肠溶片治疗中国成年反流性食管炎受试者的有效性和安全性。","market":"sh","thumbnail":null,"type":0,"news_type":0,"thumbnails":[],"rights":{"source":"stock_eastmoney","url":"http://finance.eastmoney.com/a/202603223679754978.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/202603223679754978.html","is_publish_highlight":false,"source_rank":0,"column":"","sentiment":"0","news_top_title":null,"news_tag":"","news_rank":0,"length":0,"strategy_id":0,"source":"stock_eastmoney","symbols":["00460","BK1191","BK1515","BK4134","159992","BK1593","BK1161","BK1574","BK1600","06978","III"],"isVideo":false,"video":null,"gpt_icon":0},{"id":"2621714992","title":"轩竹生物-B(02575)：安奈拉唑钠肠溶片(安久卫®)治疗反流性食管炎中国III期临床试验完成全部受试者入组","url":"https://stock-news.laohu8.com/highlight/detail?id=2621714992","media":"智通财经","labels":["productRelease"],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2621714992?lang=zh_cn&edition=fundamental","pubTime":"2026-03-22 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发布公告，公司自主研发的创新药安奈拉唑钠肠溶片用于治疗成人反流性食管炎的中国III期临床试验已于近日顺利完成全部500名受试者入组。该项III期临床试验是一项多中心、随机、双盲双模拟、阳性药物平行对照的关键性研究，旨在评估安奈拉唑钠肠溶片治疗中国成年反流性食管炎受试者的有效性和安全性。安全性指标主要为不良事件的发生类型、发生率、严重程度。","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/1417067.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":["BK4134","III","02575","BK1191"],"isVideo":false,"video":null,"gpt_icon":0},{"id":"2621719302","title":"迪哲医药(688192.SH)：舒沃哲®单药一线治疗EGFRexon20ins非小细胞肺癌国际多中心III期临床试验获阳性顶线结果","url":"https://stock-news.laohu8.com/highlight/detail?id=2621719302","media":"智通财经","labels":["dataReport"],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2621719302?lang=zh_cn&edition=fundamental","pubTime":"2026-03-22 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NSCLC一线治疗取得阳性结果的口服靶向药物。","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/1417047.html","is_publish_highlight":false,"source_rank":0,"column":"","sentiment":"2","news_top_title":null,"news_tag":"dataReport","news_rank":0,"length":0,"strategy_id":0,"source":"stock_zhitongcaijing","symbols":["III","BK0239","688192","BK4134"],"isVideo":false,"video":null,"gpt_icon":0},{"id":"2620270254","title":"康宁杰瑞制药-B(09966.HK)：JSKN016用于治疗TNBC的III期临床研究完成首例患者给药","url":"https://stock-news.laohu8.com/highlight/detail?id=2620270254","media":"中金财经","labels":["dataReport"],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2620270254?lang=zh_cn&edition=fundamental","pubTime":"2026-03-20 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Pharma启动了KITE-753的首个III期临床试验。KITE-753是一款靶向CD19和CD20的双顺反子自体CAR-T细胞疗法。研究的主要终点是第6个月实现完全缓解的患者比例和36个月内的无事件生存期。结果显示，剂量3队列，在14例未接受过CAR-T细胞疗法治疗的患者中，11例实现CR，CR率为79%;总人群，在20例未接受过CAR-T细胞疗法治疗的患者中，14例实现CR，CR率为70%。","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/1416170.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":["SG9999015945.SGD","IE00BKVL7J92.USD","III","LU0122379950.USD","LU0823416689.USD","LU0882574055.USD","LU0058720904.USD","LU0289739699.SGD","LU2112291526.USD","LU1037948897.HKD","LU1571399168.USD","LU1934455863.HKD","IE0002270589.USD","IE00B19Z3B42.SGD","LU1674673691.USD","LU1023059063.AUD","LU0965508806.USD","LU0114720955.EUR","LU0965509010.AUD","LU0965509283.SGD","LU1066051498.USD","LU1585245621.USD","SG9999015952.SGD","BK4583","LU0234570918.USD","LU1839511570.USD","SG9999015986.USD","LU0109394709.USD","LU1061106388.HKD","LU1037948541.HKD","LU0965509101.SGD","BK4022","LU1430594728.SGD","BK4134","LU0861579265.USD","BK4588","LU2089984988.USD","BK4139","BK4532","IE00B19Z3581.USD","LU1674673428.USD","LU1066053197.SGD","IE00BZ1G4Q59.USD","BK4568","LU0889565916.HKD","LU2087621335.USD","IE00B3T34201.USD","SG9999015978.USD","CAR","GILD"],"isVideo":false,"video":null,"gpt_icon":0},{"id":"2620256274","title":"开拓药业-B(09939)：KX-826酊1.0%治疗中国成年男性雄激素脱发关键性临床试验III期阶段达到主要终点","url":"https://stock-news.laohu8.com/highlight/detail?id=2620256274","media":"智通财经","labels":["productRelease"],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2620256274?lang=zh_cn&edition=fundamental","pubTime":"2026-03-18 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KX-826酊1.0%治疗脱发的关键性临床试验III期阶段已获得顶线数据。KX-826作为公司目前进展最快的外用创新药物之一，自开发以来已在中国和美国完成针对男性及女性的多项用于治疗脱发的临床试验，并表现出优异的有效性及安全性。该药物和KX-826均有望作为一种治疗雄激素性脱发的全新疗法，为广大脱发患者提供了更安全且有效的治疗选择。","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/1415598.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":["BK1161","BK1574","09939","BK4134","BK1515","III"],"isVideo":false,"video":null,"gpt_icon":1},{"id":"2620234995","title":"华海药业(600521.SH)：HB0025注射液启动子宫内膜癌III期临床试验","url":"https://stock-news.laohu8.com/highlight/detail?id=2620234995","media":"智通财经","labels":["productRelease"],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2620234995?lang=zh_cn&edition=fundamental","pubTime":"2026-03-18 18:11","pubTimestamp":1773828691,"startTime":"0","endTime":"0","summary":"智通财经APP讯，华海药业(600521.SH)公告，公司下属子公司上海华奥泰生物药业股份有限公司(“华奥泰”)就HB0025联合化疗一线治疗晚期/复发子宫内膜癌经过与国家药品监督管理局药品审评中心(“CDE”)Ⅱ期临床试验结束/Ⅲ期临床试验启动前的会议沟通，公司将正式启动HB0025注射液子宫内膜癌的Ⅲ期临床试验。","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/1415483.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":["BK0185","BK0239","BK0070","600521","BK0028","BK4134","BK0201","BK0012","III","BK0188"],"isVideo":false,"video":null,"gpt_icon":0},{"id":"1125277344","title":"美国悬赏千万美元征集伊朗高层官员情报","url":"https://stock-news.laohu8.com/highlight/detail?id=1125277344","media":"投资观察","labels":[],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/1125277344?lang=zh_cn&edition=fundamental","pubTime":"2026-03-14 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风险权重","url":"https://stock-news.laohu8.com/highlight/detail?id=2619159552","media":"链捕手","labels":["policyRegulatory"],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2619159552?lang=zh_cn&edition=fundamental","pubTime":"2026-03-13 11:02","pubTimestamp":1773370922,"startTime":"0","endTime":"0","summary":" ChainCatcher 消息，据市场消息，美联储负责监管事务的副主席米歇尔·鲍曼表示，美国监管机构将在未来几周内提出实施巴塞尔协议 III 最终阶段的规则提案，预计于 3 月 17 日至 21 日这一周发布，随后将开放 90 天的公众意见征询期。\n\n该提案由美联储与货币监理署和联邦存款保险公司协调制定。根据巴塞尔委员会 2022 年最终确定的全球加密框架，比特币被归入监管机构认为难以对冲且固有波动性的第 2b 组资产，面临 1250% 的风险权重。这意味着银行持有 1 亿美元比特币敞口，将被视为 12.5 亿美元风险加权资产，需为此持有约 1 亿美元资本。\n\n与现金、黄金和美国国债的零风险权重以及企业贷款 20%-100% 的范围相比，比特币的资本处理极为严苛。加密行业机构批评该框架将比特币错误分类，阻止银行提供相关服务。 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贝捷迈全球III期MANEUVER研究结果荣登《柳叶刀》","url":"https://stock-news.laohu8.com/highlight/detail?id=2618985985","media":"智通财经网","labels":["dataReport"],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2618985985?lang=zh_cn&edition=fundamental","pubTime":"2026-03-10 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Lancet)发布贝捷迈®全球III期MANEUVER研究结果","url":"https://stock-news.laohu8.com/highlight/detail?id=2618692617","media":"智通财经","labels":["dataReport"],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2618692617?lang=zh_cn&edition=fundamental","pubTime":"2026-03-09 08:03","pubTimestamp":1773014618,"startTime":"0","endTime":"0","summary":"智通财经APP讯，和誉-B(02256)发布公告，公司的附属公司上海和誉生物医药科技有限公司(和誉医药)宣布，其自主研发的新型、口服、高选择性且高效的小分子CSF-1R抑制剂贝捷迈®(盐酸匹米替尼胶囊，ABSK021)的全球多中心III期MANEUVER研究结果，于3月5日(西欧时间)正式发表于国际医学期刊《柳叶刀》 (The Lancet)1。此次发表标志着和誉医药这一创新疗法在临床研究质量、数据完整性及国际学术认可度方面取得了重要里程碑。","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/1411363.html","is_publish_highlight":false,"source_rank":0,"column":"","sentiment":"0","news_top_title":null,"news_tag":"dataReport","news_rank":0,"length":0,"strategy_id":0,"source":"stock_zhitongcaijing","symbols":["BK1161","LU2476274308.USD","IE00B543WZ88.USD","IE00BPRC5H50.USD","LU2778985437.USD","BK4134","02256","LU2476274720.SGD","LU2488822045.USD","III","IE00B5MMRT66.SGD"],"isVideo":false,"video":null,"gpt_icon":0},{"id":"1125385117","title":"信息服务集团发布2026年第一季度业绩指引：营收预计6050万至6150万美元，调整后EBITDA达750万至850万美元","url":"https://stock-news.laohu8.com/highlight/detail?id=1125385117","media":"美股速递","labels":["dataReport"],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/1125385117?lang=zh_cn&edition=fundamental","pubTime":"2026-03-06 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期临床","url":"https://stock-news.laohu8.com/highlight/detail?id=2617577516","media":"求实药社","labels":["productRelease"],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2617577516?lang=zh_cn&edition=fundamental","pubTime":"2026-03-05 12:03","pubTimestamp":1772683402,"startTime":"0","endTime":"0","summary":"来源：丁香园Insight数据库3 月 4 日，药物临床试验登记与信息公示平台官网显示，阿斯利康登记了一项特泽利尤单抗用于鼻内镜下鼻息肉评分 ≥4 分慢性鼻窦炎伴鼻息肉成人患者附加维持治疗的 IIIb 期临床研究。用药方案为每 4 周皮下注射一次，合计 24 周。通过精准阻断 TSLP，特泽利尤单抗可从源头抑制相关炎症通路激活，从而缓解疾病症状。目前，特泽利尤单抗已经在美国、日本、欧盟获批 2 项适应症，分别是哮喘、慢性鼻窦炎伴鼻息肉病。","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=nesSN2026030514022597a82446&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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