美股詳情

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信息服務

5.19

+0.12002.37%

成交量：15.99萬

成交額：82.86萬

市值：2.51億

市盈率：21.64

高：5.21

開：5.12

低：5.09

收：5.07

52周最高：6.45

52周最低：3.74

股本：4,841.35萬

流通股本：3,555.23萬

量比：0.94

換手率：0.45%

股息：0.18

股息率：3.47%

每股收益(TTM):0.2399

每股收益(LYR):0.1900

淨資產收益率：12.30%

總資產收益率：6.36%

市淨率：2.62

市盈率(LYR):27.32

資料載入中...

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发布公告，公司核心商业化产品舒格利单抗获得欧洲肿瘤内科学会指南的级推荐。2025年2月，舒格利单抗联合化疗已获得ESMO《非驱动基因阳性转移性非小细胞肺癌动态临床指南》的推荐，用于鳞状及非鳞状IV期非小细胞肺癌双适应症的一线治疗。至此，舒格利单抗在欧盟及英国获批的两项肺癌适应症均已被纳入ESMO指南，充分体现了其临床价值。","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/1418760.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","BK4134","III","02616","BK1161"],"isVideo":false,"video":null,"gpt_icon":0},{"id":"2621206968","title":"軒竹生物-B(02575)：吡洛西利聯合氟維司群治療HR+/HER2-晚期乳腺癌III期臨床研究最終分析結果於國際頂尖期刊《JAMA Oncology》發表","url":"https://stock-news.laohu8.com/highlight/detail?id=2621206968","media":"智通财经","labels":["dataReport"],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2621206968?lang=zh_tw&edition=fundamental","pubTime":"2026-03-24 19:12","pubTimestamp":1774350738,"startTime":"0","endTime":"0","summary":"智通财经APP讯，轩竹生物-B 发布公告，公司自主研发的新型CDK2/4/6抑制剂吡洛西利的III期BRIGHT-2临床研究最终分析结果，已于近日在国际顶尖医学期刊《美国医学会杂志·肿瘤学》正式在线全文发表。BRIGHT-2研究最终分析结果显示，吡洛西利联合氟维司群为患者带来了具有临床意义且持久稳健的获益。","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/1418161.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":["BK4134","BK4225","III","BK1191","02575","BK4203","HR"],"isVideo":false,"video":null,"gpt_icon":0},{"id":"2621406605","title":"遠大醫藥(00512)核藥戰略伙伴Telix全球首創rADC國際多中心III期獲積極進展，前列腺癌治療添新希望！","url":"https://stock-news.laohu8.com/highlight/detail?id=2621406605","media":"智通财经","labels":["corporation"],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2621406605?lang=zh_tw&edition=fundamental","pubTime":"2026-03-24 18:59","pubTimestamp":1774349976,"startTime":"0","endTime":"0","summary":"智通财经APP获悉，近日，远大医药核药领域战略合作伙伴澳洲Telix公司传来重磅利好，其用于治疗前列腺癌的全球首创的镥标记的治疗性放射性抗体药物偶联物候选药物TLX591-Tx国际多中心III期临床试验的第一部分已成功达到主要目标，证明了该产品的安全性和耐受性，且未观察到新的不良反应，不仅促进了该创新产品未来的进一步开发及上市，同时也体现了前列腺癌治疗未来有望获得全新选择。","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/1418146.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":["BK0028","BK4134","00512","000876","BK0188","BK0238","BK0196","BK0183","III","BK0187","BK0012","BK1191"],"isVideo":false,"video":null,"gpt_icon":0},{"id":"2621603174","title":"軒竹生物-B(02575)漲逾8% 安久衞治療反流性食管炎III期試驗完成全部受試者入組","url":"https://stock-news.laohu8.com/highlight/detail?id=2621603174","media":"金吾财讯","labels":["dataReport"],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2621603174?lang=zh_tw&edition=fundamental","pubTime":"2026-03-24 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":["00460","BK1515","BK1191","BK1600","III","BK4134","BK1593","02575"],"isVideo":false,"video":null,"gpt_icon":0},{"id":"2621337490","title":"康寧傑瑞製藥-B(09966)：KN026輔助治療HER2+乳腺癌III期臨床研究完成首例患者給藥","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_tw&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":"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/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":["III","BK1161","BK4134","BK1574","09966"],"isVideo":false,"video":null,"gpt_icon":0},{"id":"2621672560","title":"華萊士成立信息服務公司，註冊資本5000萬","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_tw&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":["BK4531","BK1588","BK1587","BK4585","BK4007","III","BK4588","BK1191","HCM","BK4134","00013"],"isVideo":false,"video":null,"gpt_icon":0},{"id":"2621742594","title":"宜明昂科-B(01541)成功完成IMM01(替達派西普)用於慢性粒-單核細胞白血病(CMML)一線治療的III期臨床試驗中期分析的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_tw&edition=fundamental","pubTime":"2026-03-23 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发布公告，本公司成功完成IMM01用于慢性粒-单核细胞白血病一线治疗的III期临床试验中期分析的133例患者招募。此外，IMM01的CD47结合结构域经过特别改造能够避免与人体红细胞结合。凭藉差异化的分子设计，IMM01表现出良好的安全性并证实其激活巨噬细胞的能力。IMM01联合阿扎胞苷进行CMML一线治疗于2023年11月获美国食品药品监督管理局授予的孤儿药资格认定。本集团拥有IMM01的全球知识产权及商业化权利。","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/1417114.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":["01541","BK4134","BK1161","III"],"isVideo":false,"video":null,"gpt_icon":0},{"id":"2621124714","title":"四環醫藥附屬創新藥III期臨床試驗完成500名受試者入組","url":"https://stock-news.laohu8.com/highlight/detail?id=2621124714","media":"财中社","labels":[],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2621124714?lang=zh_tw&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":"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/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":["BK1191","02575","III","BK4134"],"isVideo":false,"video":null,"gpt_icon":0},{"id":"2621719302","title":"迪哲醫藥(688192.SH)：舒沃哲®單藥一線治療EGFRexon20ins非小細胞肺癌國際多中心III期臨床試驗獲陽性頂線結果","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_tw&edition=fundamental","pubTime":"2026-03-22 15:43","pubTimestamp":1774165425,"startTime":"0","endTime":"0","summary":"智通财经APP讯，迪哲医药(688192.SH)公告，公司自主研发的产品舒沃哲®(ZEGFROVY®，通用名：舒沃替尼片)单药一线治疗表皮生长因子受体(EGFR)20号外显子插入突变(exon20ins)晚期非小细胞肺癌(NSCLC)的国际多中心III期临床研究“悟空28”(WU-KONG28)达到主要研究终点、取得阳性顶线结果，是全球首个且唯一在国际多中心随机对照III期临床研究中，针对EGFRexon20ins 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":["688192","III","BK4134","BK0239"],"isVideo":false,"video":null,"gpt_icon":0},{"id":"2620270254","title":"康寧傑瑞製藥-B(09966.HK)：JSKN016用於治療TNBC的III期臨床研究完成首例患者給藥","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_tw&edition=fundamental","pubTime":"2026-03-20 08:17","pubTimestamp":1773965823,"startTime":"0","endTime":"0","summary":"格隆汇3月20日丨康宁杰瑞制药-B发布公告，JSKN016用于治疗三阴性乳腺癌的一项III期临床研究已成功完成首例患者给药。TNBC约占所有BC病例的15%至20%。　　JSKN016-301是一项开放、随机、对照、多中心III期临床研究，预计将在中国约60家临床研究中心开展。该研究计划入组经至少二线系统性治疗失败的不可手术切除的局部晚期、复发或转移性TNBC患者。","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://sc.stock.cnfol.com/gushizhibo/20260320/32083524.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":"zhongjincaijing_highlight","symbols":["III","BK1574","BK1161","BK4134","09966"],"isVideo":false,"video":null,"gpt_icon":0},{"id":"2620225813","title":"吉利德科學(GILD.US)CD19/CD20 CAR-T細胞療法啓動III期臨床","url":"https://stock-news.laohu8.com/highlight/detail?id=2620225813","media":"智通财经","labels":["dataReport"],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2620225813?lang=zh_tw&edition=fundamental","pubTime":"2026-03-19 21:12","pubTimestamp":1773925932,"startTime":"0","endTime":"0","summary":"智通财经APP获悉，3月18日，美国临床试验收录网站显示，吉利德科学旗下公司Kite 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":"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/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":["LU0889565916.HKD","LU1066053197.SGD","SG9999015978.USD","LU0965509283.SGD","III","LU1037948897.HKD","GILD","IE0002270589.USD","CAR","LU0965509101.SGD","LU1066051498.USD","IE00B19Z3B42.SGD","LU1674673691.USD","LU0861579265.USD","LU0965509010.AUD","BK4532","BK4568","LU1430594728.SGD","BK4139","BK4022","IE00BKVL7J92.USD","LU0114720955.EUR","LU0965508806.USD","LU1023059063.AUD","LU2087621335.USD","LU0882574055.USD","LU1585245621.USD","BK4134","IE00B19Z3581.USD","IE00BZ1G4Q59.USD","LU0058720904.USD","BK4583","LU1674673428.USD","LU1934455863.HKD","LU1037948541.HKD","LU1839511570.USD","LU2112291526.USD","SG9999015952.SGD","LU0109394709.USD","LU2089984988.USD","IE00B3T34201.USD","SG9999015986.USD","LU0122379950.USD","LU1571399168.USD","LU0823416689.USD","BK4588","LU0289739699.SGD","LU0234570918.USD","LU1061106388.HKD","SG9999015945.SGD"],"isVideo":false,"video":null,"gpt_icon":0},{"id":"2620256274","title":"開拓藥業-B(09939)：KX-826酊1.0%治療中國成年男性雄激素脱髮關鍵性臨床試驗III期階段達到主要終點","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_tw&edition=fundamental","pubTime":"2026-03-18 20:59","pubTimestamp":1773838785,"startTime":"0","endTime":"0","summary":"智通财经APP讯，开拓药业-B 发布公告，其自主研发、潜在同类首创的 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":"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/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":["BK1574","III","BK1515","BK1161","BK4134","09939"],"isVideo":false,"video":null,"gpt_icon":1},{"id":"2620234995","title":"華海藥業(600521.SH)：HB0025注射液啓動子宮內膜癌III期臨床試驗","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_tw&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":"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/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":["BK0028","BK0012","BK4134","BK0188","600521","BK0201","III","BK0239","BK0185","BK0070"],"isVideo":false,"video":null,"gpt_icon":0}],"pageSize":20,"totalPage":9,"pageCount":9,"totalSize":176,"code":"91000000","status":"200"}]}}