美股详情

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信息服务

5.38

0.0000

盘后：5.380.00000.00%16:15 EDT

成交量：16.47万

成交额：88.71万

市值：2.60亿

市盈率：22.43

高：5.44

开：5.32

低：5.32

收：5.38

52周最高：6.45

52周最低：3.74

股本：4,841.35万

流通股本：3,555.23万

量比：0.96

换手率：0.46%

股息：0.18

股息率：3.35%

每股收益(TTM):0.2399

每股收益(LYR):0.1900

净资产收益率：12.30%

总资产收益率：6.36%

市净率：2.72

市盈率(LYR):28.32

数据加载中...

总览公司新闻资讯公告

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来凯LAE002乳腺癌III期临床达到主要终点

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来凯医药-B(02105)：LAE 002(Afuresertib)III期临床试验(AFFIRM-205)达到无进展生存期(PFS)的主要终点

轩竹生物-B(02575)：安奈拉唑钠新适应症获批开展III期临床试验

港股异动 | 再鼎医药(09688)涨超3% 近日与安进达成全球临床合作 Zoci正处于全球注册性临床III期阶段

港股异动 | 科笛-B(02487)涨超3% CU-20101（注射用A型肉毒毒素）完成中国III期临床试验

做好信息服务破解人岗错配

科笛-B(02487)：CU-20101(注射用A型肉毒毒素)用于改善中度至重度眉间纹完成中国III期临床试验

深桑达Ａ：公司研发重点围绕数字与信息服务业务中的“云数智”相关产品

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美国对失踪飞行员信息泄露事件展开调查

西藏自治区互联网新闻信息服务单位许可信息

中国西藏新闻网

百利天恒：iza-bren联合用药获2个II/III期临床试验批准

每日经济新闻

港股异动 | 欧康维视生物-B(01477)午后涨超16% OT-211治疗干眼症III期临床试验完成首例患者入组

康宁杰瑞制药-B(09966)：KN026新辅助治疗HER2阳性乳腺癌III期临床研究达到主要终点

宜明昂科-B(01541)：IMM0306治疗复发性╱难治性滤泡性淋巴瘤的III期临床试验完成首例患者给药

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发布公告，集团已在2026年4月17日至2026年4月22日举行的2026年美国癌症研究协会年会以口头报告的形式展示地罗阿克一线治疗间变性淋巴瘤激酶阳性晚期非小细胞肺癌的临床III期研究结果。DIAMOND-2研究是一项在中国境内开展的多中心、随机、开放标签的III期临床研究，以克唑替尼作为对照，旨在头对头评估地罗阿克相较克唑替尼在一线治疗ALK阳性晚期NSCLC患者的有效性与安全性。","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/1430365.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":["BK4134","ALK","III","02575","BK1191","BK4500","BK4588","BK4585","BK4008"],"isVideo":false,"video":null,"gpt_icon":0},{"id":"2628227042","title":"药捷安康-B(02617)：替恩戈替尼单药治疗晚期胆管癌患者确证性III期临床完成首例患者给药","url":"https://stock-news.laohu8.com/highlight/detail?id=2628227042","media":"智通财经","labels":[],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2628227042?lang=zh_cn&edition=fundamental","pubTime":"2026-04-17 18:41","pubTimestamp":1776422489,"startTime":"0","endTime":"0","summary":"智通财经APP讯，药捷安康-B(02617)公布，公司核心产品替恩戈替尼(Tinengotinib, TT-00420)单药治疗晚期胆管癌患者的确证性III期临床研究，于近日完成首例患者给药。本试验为在中国开展的一项评价替恩戈替尼对比化疗用于既往经一线系统性治疗后复发或进展的、携带FGFR2融合╱重排或突变的、手术不可切除的晚期或转移性肝内胆管癌患者的疗效与安全性的随机对照、开放、多中心III期临床研究。","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/1430049.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_zhitongcaijing","symbols":["BK1161","BK4134","02617","III"],"isVideo":false,"video":null,"gpt_icon":0},{"id":"2627987288","title":"来凯LAE002乳腺癌III期临床达到主要终点","url":"https://stock-news.laohu8.com/highlight/detail?id=2627987288","media":"医药地理","labels":[],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2627987288?lang=zh_cn&edition=fundamental","pubTime":"2026-04-15 17:09","pubTimestamp":1776244140,"startTime":"0","endTime":"0","summary":"4月15日，来凯医药宣布，LAE002联合氟维司群，治疗HR+/HER2-乳腺癌III期临床试验取得强有力的积极顶线结果，成功达到其主要终点。临床结果显示，LAE002联合氟维司群组的中位无进展生存期为7.6个月，安慰剂联合氟维司群组为2.0个月，风险比为0.33。每日一次口服LAE002的患者耐受性良好，因不良事件停药比例极低；整体安全性特征与此前联合疗法评估数据一致。齐鲁制药获得在中国进行LAE002的研究、开发及商业化的独家许可。","market":"sg","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/relnews/hk/2026-04-15/doc-inhuqnca3537414.shtml","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":"sina","symbols":["BK4134","III"],"isVideo":false,"video":null,"gpt_icon":0},{"id":"2627407539","title":"中国生物制药(01177)：维特柯妥拜单抗“CLDN18.2 ADC”一线胃及胃食管交界部腺癌III期临床试验完成首例患者入组","url":"https://stock-news.laohu8.com/highlight/detail?id=2627407539","media":"智通财经","labels":[],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2627407539?lang=zh_cn&edition=fundamental","pubTime":"2026-04-15 17:02","pubTimestamp":1776243779,"startTime":"0","endTime":"0","summary":"本研究为LM-302开展的第二项Ⅲ期临床试验，也是全球首个CLDN18.2 ADC药物采用无化疗方案用于胃癌一线治疗的Ⅲ期临床试验。这种“ADC+免疫”联合策略有望为CLDN18.2阳性胃癌患者带来更深度的肿瘤缓解。除本次启动的LM-302联合疗法用于一线治疗CLDN18.2阳性GC/GEJ的III期临床外，LM-302单药用于三线及以上CLDN18.2阳性GC/GEJ的III期临床研究已完成全部受试者入组。","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/1428818.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":["ADC","BK1191","01177","BK1589","BK4134","BK1521","BK4231","HK0000165453.HKD","BK4080","IE00BZ08YT58.USD","IE00BZ08YS42.EUR","III","BK1515","IE00BZ08YR35.GBP"],"isVideo":false,"video":null,"gpt_icon":0},{"id":"2627473918","title":"来凯医药-B(02105)：LAE 002(Afuresertib)III期临床试验(AFFIRM-205)达到无进展生存期(PFS)的主要终点","url":"https://stock-news.laohu8.com/highlight/detail?id=2627473918","media":"智通财经","labels":["dataReport"],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2627473918?lang=zh_cn&edition=fundamental","pubTime":"2026-04-15 08:22","pubTimestamp":1776212528,"startTime":"0","endTime":"0","summary":"II期临床试验是一项多中心、随机、双盲、安慰剂对照的关键性研究，旨在评估该联合疗法的抗肿瘤疗效及安全性。.每日一次口服LAE 002的治疗，患者耐受性良好，因不良事件而中止治疗的比例极低。本集团有权就许可区域内LAE 002的未来净销售额收取梯度销售分成，分成比率在十余个百分点至二十余个百分点。本集团计划在中国以外地区寻求战略合作伙伴，以加速LAE 002在国际市场的开发及商业化。","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/1428595.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":["BK4211","III","BK1161","BK4195","PFS","BK4134","02105"],"isVideo":false,"video":null,"gpt_icon":0},{"id":"2627427789","title":"轩竹生物-B(02575)：安奈拉唑钠新适应症获批开展III期临床试验","url":"https://stock-news.laohu8.com/highlight/detail?id=2627427789","media":"智通财经","labels":["productRelease"],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2627427789?lang=zh_cn&edition=fundamental","pubTime":"2026-04-15 06:34","pubTimestamp":1776206064,"startTime":"0","endTime":"0","summary":"智通财经APP讯，轩竹生物-B 发布公告，本集团自主研发的创新药安奈拉唑钠肠溶片近日获得中国国家药品监督管理局药品审评中心批准，开展含安奈拉唑钠肠溶片的铋剂四联疗法根除幽门螺杆菌的III期临床研究。本次安奈拉唑钠新适应症III期临床试验申请获批，有助于拓展产品适应症范围，提升本公司在消化疾病治疗领域的影响力，对本公司长远发展及商业化布局具有重要意义。","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/1428565.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":["02575","BK1191","BK4134","III"],"isVideo":false,"video":null,"gpt_icon":0},{"id":"2627498112","title":"港股异动 | 再鼎医药(09688)涨超3% 近日与安进达成全球临床合作 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pelitecan联合安进IMDELLTRA，一款靶向DLL3的双特异性T细胞衔接器疗法，用于治疗广泛期小细胞肺癌患者。作为该合作协议的一部分，安进将申办一项全球1b期研究，评估zoci联合IMDELLTRA在ES-SCLC患者中的安全性和有效性。再鼎医药将保留zoci的完整所有权，并将向安进提供临床研究用药。","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/1428082.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":["LU0289739699.SGD","BK4531","IE0009355771.USD","III","BK4599","IE00B2B36J28.USD","IE00B4R5TH58.HKD","LU1057294990.SGD","BK1588","LU0122379950.USD","09688","BK4533","LU1023059063.AUD","LU2112291526.USD","BK4534","LU2468319806.SGD","BK4139","LU2242646821.SGD","LU1983299246.USD","AMGN","LU2089984988.USD","BK1574","LU2488822045.USD","LU0320765992.SGD","BK4134","BK4548","LU0889565916.HKD","IE00BJJMRZ35.SGD","IE00BJT1NW94.SGD","VXUS","IE00BFTCPJ56.SGD","LU0109394709.USD","LU1571399168.USD","BK4581","BK4566","BK4585","LU2242652126.USD","LU0868494617.USD","BK1161","BK4526","LU0058720904.USD","ZLAB","IE0002141913.USD","SG9999001440.SGD","LU1061106388.HKD","BK4588"],"isVideo":false,"video":null,"gpt_icon":0},{"id":"2627481537","title":"港股异动 | 科笛-B(02487)涨超3%  CU-20101（注射用A型肉毒毒素）完成中国III期临床试验","url":"https://stock-news.laohu8.com/highlight/detail?id=2627481537","media":"智通财经","labels":["productRelease"],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2627481537?lang=zh_cn&edition=fundamental","pubTime":"2026-04-13 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发布公告，本集团完成CU-20101用于改善中度至重度眉间纹的中国III期临床试验。在安全性方面，CU-20101的整体安全性良好，未发生导致提前煺出试验或导致死亡的不良事件，且未发生治疗有关的严重不良事件。CU-20101与BOTOX的安全性评估情况相近，未出现新的安全性信号。CU-20101多次重复注射给药后的有效性及安全性表现与单次用药相似。CU-20101将进一步丰富本集团的皮肤产品矩阵，并有利于与本集团现有产品形成协同效应。","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/1427503.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_zhitongcaijing","symbols":["BK1161","III","02487","BK4134"],"isVideo":false,"video":null,"gpt_icon":0},{"id":"2626188654","title":"深桑达Ａ：公司研发重点围绕数字与信息服务业务中的“云数智”相关产品","url":"https://stock-news.laohu8.com/highlight/detail?id=2626188654","media":"中金财经","labels":[],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2626188654?lang=zh_cn&edition=fundamental","pubTime":"2026-04-09 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35兆瓦地热电站投入商业运营","url":"https://stock-news.laohu8.com/highlight/detail?id=2626975845","media":"智通财经","labels":["corporation"],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2626975845?lang=zh_cn&edition=fundamental","pubTime":"2026-04-09 07:54","pubTimestamp":1775692490,"startTime":"0","endTime":"0","summary":"智通财经APP讯，开山股份(300257.SZ)公告，公司下属公司Orpower Twenty Two Limited公司(简称“Orpower22”)顺利完成了肯尼亚Menengai III 35兆瓦地热电站的可靠性测试，该电站机组调试、测试工作已圆满结束。Menengai III 35兆瓦地热电站已于2026年3月10日正式投入商业运营。","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/1426300.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":["III","BK4134","BK0117","BK0259","BK0196","BK0188","300257","BK0070"],"isVideo":false,"video":null,"gpt_icon":0},{"id":"1105607138","title":"众议院民主党人要求紧急投票以阻止“第三次世界大战”","url":"https://stock-news.laohu8.com/highlight/detail?id=1105607138","media":"投资观察","labels":[],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/1105607138?lang=zh_cn&edition=fundamental","pubTime":"2026-04-08 02:02","pubTimestamp":1775584951,"startTime":"0","endTime":"0","summary":"众议院民主党高层呼吁议员立即返回华盛顿，就终止伊朗战争进行投票。由纽约州民主党领袖哈基姆·杰弗里斯及其他众议院民主党主要议员联合签署的声明指出，特朗普总统已“完全失控”，必须通过投票阻止其“将国家拖入第三次世界大战”。\n目前众议院休会至下周一。今年三月，一项反对伊朗战争的两党《战争权力决议案》曾以212票赞成、219票反对的结果在众议院被否决，当时议员投票结果基本按党派划线划分。\n（本文结束）道琼斯通讯社\n2026年4月7日 14:01 ET（18:01 GMT）\n版权所有（c）2026 道琼斯公司","market":"hk","thumbnail":"","type":0,"news_type":0,"thumbnails":[],"rights":null,"property":[],"language":"zh","translate_title":"","themeId":null,"theme_name":"","theme_type":"","isJumpTheme":false,"source_url":"","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":null,"symbols":["BK4134","III"],"isVideo":false,"video":null,"gpt_icon":0},{"id":"1175143092","title":"美国对失踪飞行员信息泄露事件展开调查","url":"https://stock-news.laohu8.com/highlight/detail?id=1175143092","media":"投资观察","labels":[],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/1175143092?lang=zh_cn&edition=fundamental","pubTime":"2026-04-07 01:34","pubTimestamp":1775496862,"startTime":"0","endTime":"0","summary":"美国总统特朗普表示，当局已启动调查程序，追查有关失踪飞行员的信息如何被泄露给媒体。\"我们正在全力追查泄密者，\"他表态称。特朗普指责相关报道危及了在伊朗开展的救援行动。\n特朗普透露，计划要求首家报道救援行动的媒体公司公开其消息来源，但未具体点名涉事机构。\"要么交出线人，要么面临牢狱之灾，\"总统警告称，\"他们的行为不仅将那名飞行员置于险境，更连累了数百名参与搜救的人员。\"\n（本文源自道琼斯通讯社实时报道合集，完整内容可通过检索代码P/WSJL获取）\n（报道截止时间：2026年4月6日13:32美国东部时间/17:32格林威治时间）","market":"hk","thumbnail":"","type":0,"news_type":0,"thumbnails":[],"rights":null,"property":[],"language":"zh","translate_title":"","themeId":null,"theme_name":"","theme_type":"","isJumpTheme":false,"source_url":"","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":null,"symbols":["III","BK4134"],"isVideo":false,"video":null,"gpt_icon":0},{"id":"2624017509","title":"西藏自治区互联网新闻信息服务单位许可信息","url":"https://stock-news.laohu8.com/highlight/detail?id=2624017509","media":"中国西藏新闻网","labels":[],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2624017509?lang=zh_cn&edition=fundamental","pubTime":"2026-04-02 20:35","pubTimestamp":1775133300,"startTime":"0","endTime":"0","summary":"截至2026年3月31日，经西藏自治区互联网信息办公室审批的互联网新闻信息服务单位总计86家，具体服务形式包括：互联网站19个、应用程序14个、公众账号440个，共计473个服务项。","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":"https://finance.sina.com.cn/jjxw/2026-04-02/doc-inhtcnfv4278286.shtml","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":"sina","symbols":["III","159792","160636","BK4134"],"isVideo":false,"video":null,"gpt_icon":0},{"id":"2624123594","title":"百利天恒：iza-bren联合用药获2个II/III期临床试验批准","url":"https://stock-news.laohu8.com/highlight/detail?id=2624123594","media":"每日经济新闻","labels":["productRelease"],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2624123594?lang=zh_cn&edition=fundamental","pubTime":"2026-04-01 18:06","pubTimestamp":1775038011,"startTime":"0","endTime":"0","summary":"每经AI快讯，4月1日，百利天恒(688506.SH)公告称，公司近日收到国家药监局签发的2个《药物临床试验批准通知书》，公司自主研发的创新生物药iza-bren(EGFR×HER3双抗ADC)的2个联合用药方案获得批准。获批适应症包括：联合阿比特龙±奥拉帕利、联合奥拉帕利用于去势抵抗性前列腺癌；联合贝伐珠单抗±化疗、联合奥拉帕利±贝伐珠单抗±化疗用于晚期卵巢癌。","market":"us","thumbnail":null,"type":0,"news_type":0,"thumbnails":[],"rights":{"source":"stock_eastmoney","url":"http://finance.eastmoney.com/a/202604013692048171.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/202604013692048171.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_eastmoney","symbols":["688506","02615","III","BK4134","91194","BK0239"],"isVideo":false,"video":null,"gpt_icon":0},{"id":"2624562436","title":"港股异动 | 欧康维视生物-B(01477)午后涨超16% OT-211治疗干眼症III期临床试验完成首例患者入组","url":"https://stock-news.laohu8.com/highlight/detail?id=2624562436","media":"智通财经","labels":["dataReport"],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2624562436?lang=zh_cn&edition=fundamental","pubTime":"2026-04-01 14:26","pubTimestamp":1775024786,"startTime":"0","endTime":"0","summary":"智通财经APP获悉，欧康维视生物-B午后涨超16%，截至发稿，涨15.33%，报8.5港元，成交额2606.87万港元。消息面上，欧康维视生物发布公告称，OT-211在中国开展的III期临床试验已完成首例患者入组。首例患者成功入组标志着OT-211在中国的临床开发取得重要里程碑进展，并体现了集团致力于为DED患者推进创新疗法。公开资料显示，Alcon Inc.开发出AR-15512的0.003%浓度滴眼液配方，并完成一项IIb期及三项III期临床试验。OT-211已于2025年5月28日获FDA批准用于治疗DED的体征及症状。","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/1423857.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":["01477","BK4588","BK4134","BK1574","BK1191","VXUS","BK4585","III"],"isVideo":false,"video":null,"gpt_icon":0},{"id":"2623583940","title":"康宁杰瑞制药-B(09966)：KN026新辅助治疗HER2阳性乳腺癌III期临床研究达到主要终点","url":"https://stock-news.laohu8.com/highlight/detail?id=2623583940","media":"智通财经","labels":["productRelease"],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2623583940?lang=zh_cn&edition=fundamental","pubTime":"2026-03-31 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00:28","pubTimestamp":1774888085,"startTime":"0","endTime":"0","summary":"智通财经APP讯，宜明昂科-B 发布公告，IMM0306联合来那度胺治疗复发性╱难治性滤泡性淋巴瘤的III期临床试验顺利完成首例患者给药。由本集团独立研发的IMM0306是一种靶向分化簇47 及分化簇20 的双特异性分子，是全球首个进入临床阶段的CD47和CD20双靶向双特异性分子。截至本公告日期，本集团拥有IMM0306的全球知识产权及商业化权利。","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/1422402.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":["III","BK4134","01541","BK1161"],"isVideo":false,"video":null,"gpt_icon":0}],"pageSize":20,"totalPage":9,"pageCount":8,"totalSize":175,"code":"91000000","status":"200"}]}}