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Ashland
64.16
+1.03
1.63%
成交量:
63.51万
成交额:
4,074.10万
市值:
29.36亿
市盈率:
-4.24
高:
64.55
开:
63.49
低:
63.49
收:
63.13
52周最高:
67.39
52周最低:
45.21
股本:
4,576.21万
流通股本:
4,177.35万
量比:
0.71
换手率:
1.52%
股息:
1.65
股息率:
2.57%
每股收益(TTM):
-15.1257
每股收益(LYR):
-18.3696
净资产收益率:
-29.98%
总资产收益率:
2.09%
市净率:
1.56
市盈率(LYR):
-3.49
数据加载中...
总览
公司
新闻资讯
公告
美国研究综述-阿美特克、可口可乐、百事可乐
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·
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美股速递
·
02/03
亚什兰集团预计全年将遵循典型季节性节奏 商业活动与运营效率提升推动下半年业绩走强
美股速递
·
02/03
财报前瞻|Ashland本季度营收预计降至4.02亿美元,机构观点偏谨慎
财报Agent
·
01/26
5000亿!一战封神,他是中国最成功的美国人
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·
01/25
重磅!前中金研究所董事总经理带队,企业IPO申请火速获受理!董秘也来自中金!
市场资讯
·
2025/12/24
2025 ASH | 强生公布 CD19/CD20 双靶点 CAR-T 1b 期最新临床进展与生物标志物分析!
医麦客
·
2025/12/24
迪哲医药ASH大会发布高瑞哲®与Birelentinib淋巴瘤治疗最新积极数据
中金财经
·
2025/12/10
股海导航_2025年12月10日_沪深股市公告与交易提示
股市直击
·
2025/12/10
财经早报:光伏行业酝酿第四次洗牌 4个一线城市二手房大卖创4年新高丨2025年12月10日
新浪证券
·
2025/12/10
港股异动 | 维立志博-B(09887)涨超3% LBL-034突破性数据于2025 ASH年会口头报告发布
智通财经
·
2025/12/09
【直击2025 ASH】亚盛医药耐立克®治疗TKI耐药/不耐受CML-CP患者的注册II期研究4年随访数据亮相,长期疗效和安全性优势再获证实
美通社
·
2025/12/09
【直击2025 ASH】亚盛医药耐立克®二线治疗CML-CP临床研究数据更新,更前线治疗潜力明显
美通社
·
2025/12/09
【直击2025 ASH】亚盛医药耐立克®治疗初治Ph+ ALL患者注册III期研究(POLARIS-1)数据国际首发, 最佳MRD阴性完全缓解率超60%
美通社
·
2025/12/09
Syndax公布AML联合疗法强劲数据
环球市场播报
·
2025/12/08
吉利德Anito-cel 神经毒性低,2年多发性骨髓瘤生存率高 | ASH25
Minhua笔记
·
2025/12/08
【直击2025 ASH】亚盛医药Bcl-2抑制剂利生妥®治疗维奈克拉经治髓系肿瘤患者的Ib/II期研究数据积极,全球竞争力持续显现
美通社
·
2025/12/08
ASH 2025口头报告:信达生物公布其三特异性抗体 -IBI3003治疗复发或难治性多发性骨髓瘤患者的首次人体试验的初步数据
美通社
·
2025/12/08
金斯瑞生物科技(01548):传奇宣布于2025年ASH年会上公布报告
智通财经
·
2025/12/07
维立志博-B(09887):LBL-034临床数据于第67届ASH年会发布
智通财经
·
2025/12/07
更多
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韩翔州2010年,旧金山的一次私人聚会上,已在中国创业有成的美国人欧雷强,结识了已在美国功成名就的中国人王晓东。终于在年底,他们决定一起冒险:在中国建立一家世界级的生物科技公司,在中国做创新药卖给全世界。作为一名连续创业者,欧雷强的履历堪称完美。事实证明,中国没有辜负欧雷强的眼光。欧雷强预见到,中国的监管环境即将迎来一场有利于创新药的剧变。","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":"https://www.lanjinger.com/d/1769137313695679325","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":"lanjinger_stock","symbols":["PFS","LU1969619763.USD","BK4211","ASH","BK1500","BK4195","LU1251922891.USD","LU1719994722.HKD","BK1583","BMS","BK1161","LU1770034418.SGD","BK4109","LU0307460666.USD","06160","BK1588","LU0588546209.SGD","ORR","LU1303224171.USD","LU2463526074.USD","LU2328871848.SGD"],"gpt_icon":0},{"id":"2593440742","title":"重磅!前中金研究所董事总经理带队,企业IPO申请火速获受理!董秘也来自中金!","url":"https://stock-news.laohu8.com/highlight/detail?id=2593440742","media":"市场资讯","labels":[],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2593440742?lang=zh_cn&edition=fundamental","pubTime":"2025-12-24 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期最新临床进展与生物标志物分析!","url":"https://stock-news.laohu8.com/highlight/detail?id=2593720654","media":"医麦客","labels":["productRelease"],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2593720654?lang=zh_cn&edition=fundamental","pubTime":"2025-12-24 07:20","pubTimestamp":1766532031,"startTime":"0","endTime":"0","summary":"2025 年 12 月 24 日医麦客新闻 eMedClub News本月 9 日,强生在第 65 届美国血液学会年会上以口头报告形式,更新了其双靶点 CAR-T 疗法 Prizlo-cel的 1b 期临床试验数据及生物标志物关联分析。目前也仅有约 40% 的患者通过现有的单抗原靶向 CD19 CAR-T 细胞疗法获得长期缓解。ORR 达 91%,CR 率 75% 该数据显著优于传统 CD19 CAR-T 历史数据。Grade 3 中位数略高,但 Grade 1 和 Grade 2 中同样有高峰值浓度样本,并未显示 ICANS 严重程度与 CAR-T 细胞扩增有显著关联。","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=nesSN20251224072631a470912f&s=b","rn_cache_url":null,"customStyle":"body{padding-top:10px;}#news_title{font-weight:bold;#titleStyle#;}#news_description 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迪哲(江苏)医药股份有限公司在第67届美国临床血液学会年会上,公布了其两款全球首创新药在淋巴瘤治疗领域的最新临床研究进展。另一方面,其非共价LYN/BTK双靶点抑制剂Birelentinib在B细胞淋巴瘤领域取得新进展。公司同时披露了Birelentinib联合疗法治疗弥漫性大B细胞淋巴瘤的后续研究计划。这些数据进一步验证了迪哲医药两款核心产品的临床价值,为其在淋巴瘤治疗领域的商业化前景提供了支持。","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://sc.stock.cnfol.com/ggzixun/20251210/31856740.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":"zhongjincaijing_highlight","symbols":["ASH","BK4109","688192","BK0239","LU2463526074.USD"],"gpt_icon":0},{"id":"2590373303","title":"股海导航_2025年12月10日_沪深股市公告与交易提示","url":"https://stock-news.laohu8.com/highlight/detail?id=2590373303","media":"股市直击","labels":[],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2590373303?lang=zh_cn&edition=fundamental","pubTime":"2025-12-10 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4个一线城市二手房市场大力度复苏了。","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/y/2025-12-10/doc-inhahhpm2297001.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":["BK0149","BK0228","BK0277","BK0004","02255","BK0028","LU2463526074.USD","BK1241","BK0012","BK0102","BK0098","ASH","603815","BK4109","600576","BK0095","BK0083","BK0211"],"gpt_icon":0},{"id":"2590390894","title":"港股异动 | 维立志博-B(09887)涨超3% LBL-034突破性数据于2025 ASH年会口头报告发布","url":"https://stock-news.laohu8.com/highlight/detail?id=2590390894","media":"智通财经","labels":["productRelease"],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2590390894?lang=zh_cn&edition=fundamental","pubTime":"2025-12-09 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ASH】亚盛医药耐立克®二线治疗CML-CP临床研究数据更新,更前线治疗潜力明显","url":"https://stock-news.laohu8.com/highlight/detail?id=2590316824","media":"美通社","labels":[],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2590316824?lang=zh_cn&edition=fundamental","pubTime":"2025-12-09 09:34","pubTimestamp":1765244040,"startTime":"0","endTime":"0","summary":"此次公布是对该研究在2024 ASH年会口头报告结果的持续更新,展现了更长时间的随访疗效与安全性特征。此次更新的研究结果进一步提示耐立克有望为二线CML-CP患者带来一种安全有效的治疗选择,尤其对那些一线使用二代BCR-ABL1酪氨酸激酶抑制剂治疗失败的患者。此次数据的更新,进一步体现了耐立克为更广泛的CML患者群体提供安全有效治疗选择的潜力。","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":"https://wwwold.prnasia.com/story/archive/4842159_ZH42159_1","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":"prnasia","symbols":["BK1574","06855","LU2463526074.USD","CP","BK4585","LU1261432733.SGD","BK4016","AAPG","ASH","BK4139","BK1161","BK4109","BK4588"],"gpt_icon":0},{"id":"2590316827","title":"【直击2025 ASH】亚盛医药耐立克®治疗初治Ph+ ALL患者注册III期研究(POLARIS-1)数据国际首发, 最佳MRD阴性完全缓解率超60%","url":"https://stock-news.laohu8.com/highlight/detail?id=2590316827","media":"美通社","labels":["dataReport"],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2590316827?lang=zh_cn&edition=fundamental","pubTime":"2025-12-09 09:22","pubTimestamp":1765243320,"startTime":"0","endTime":"0","summary":"此次展示的POLARIS-1研究数据体现了耐立克在Ph+ ALL治疗领域的巨大潜力。数据显示,在诱导治疗3个周期内,耐立克联合低强度化疗在初治Ph+ ALL患者中的最佳微小残留病阴性率和MRD阴性完全缓解率分别为66.0%和64.2%;同时显示出良好的安全性。","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":"https://wwwold.prnasia.com/story/archive/4842157_ZH42157_1","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":"prnasia","symbols":["BK1574","III","ASH","BK4109","BK4588","BK4533","LU1571399168.USD","BK4107","AAPG","BK4139","LU0985320562.USD","ALL","BK1161","06855","BK4585","LU2355687059.USD","LU2463526074.USD","LU1699723380.USD","BK4134"],"gpt_icon":0},{"id":"2589272354","title":"Syndax公布AML联合疗法强劲数据","url":"https://stock-news.laohu8.com/highlight/detail?id=2589272354","media":"环球市场播报","labels":["dataReport"],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2589272354?lang=zh_cn&edition=fundamental","pubTime":"2025-12-08 23:42","pubTimestamp":1765208520,"startTime":"0","endTime":"0","summary":"美股周一早盘,临床阶段的生物制药公司Syndax(SNDX)股价下跌3.2%。该公司在2025年美国血液学会(ASH)年会上展示了revumenib联合疗法的最新数据,在新诊断和移植后急性髓系白血病患者队列中显示出高缓解率和高微小残留病阴性率。\n\n\n海量资讯、精准解读,尽在新浪财经APP\n\n责任编辑:张俊 SF065","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/usstock/c/2025-12-08/doc-inhachkx2122015.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":["LU2463526074.USD","SNDX","ASH","BK4139","BK4109"],"gpt_icon":0},{"id":"2590451393","title":"吉利德Anito-cel 神经毒性低,2年多发性骨髓瘤生存率高 | ASH25","url":"https://stock-news.laohu8.com/highlight/detail?id=2590451393","media":"Minhua笔记","labels":["dataReport"],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2590451393?lang=zh_cn&edition=fundamental","pubTime":"2025-12-08 11:58","pubTimestamp":1765166299,"startTime":"0","endTime":"0","summary":"在ASH 2025年会上,吉利德旗下Kite Pharma公布Anito-cel在iMMagine-1 II期试验中的更新数据,该靶向BCMA的CAR-T疗法在复发/难治性多发性骨髓瘤患者中显示96% ORR、74% sCR/CR率、95% MRD阴性率,中位随访15.9个月,缓解持续。III期iMMagine-3试验正在招募中,该研究将Anito-cel与标准治疗比较,预计2026年获得数据;该药物获FDA快速通道、孤儿药和RMAT资格。ICANS 发生率为 8%,其中 1 例为 3 级;其余均为 2 级或更低。","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=nesSN20251208144817a43ac231&s=b","rn_cache_url":null,"customStyle":"body{padding-top:10px;}#news_title{font-weight:bold;#titleStyle#;}#news_description 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ASH】亚盛医药Bcl-2抑制剂利生妥®治疗维奈克拉经治髓系肿瘤患者的Ib/II期研究数据积极,全球竞争力持续显现","url":"https://stock-news.laohu8.com/highlight/detail?id=2589848384","media":"美通社","labels":["dataReport"],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2589848384?lang=zh_cn&edition=fundamental","pubTime":"2025-12-08 09:58","pubTimestamp":1765159080,"startTime":"0","endTime":"0","summary":"此次数据进一步验证了利生妥在恶性髓系肿瘤领域所具备的稳健疗效与良好安全性。利生妥是亚盛医药自主研发的新型口服Bcl-2选择性抑制剂,通过选择性抑制Bcl-2蛋白,恢复癌细胞的正常凋亡过程,从而达到治疗肿瘤的目的。期待利生妥在未来,能为髓系恶性肿瘤治疗领域带来新的突破。","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":"https://wwwold.prnasia.com/story/archive/4841048_ZH41048_1","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":"prnasia","symbols":["ASH","BK4139","BK1161","BK1574","BK4109","06855","LU2463526074.USD","AAPG"],"gpt_icon":0},{"id":"2589384810","title":"ASH 2025口头报告:信达生物公布其三特异性抗体 -IBI3003治疗复发或难治性多发性骨髓瘤患者的首次人体试验的初步数据","url":"https://stock-news.laohu8.com/highlight/detail?id=2589384810","media":"美通社","labels":["productRelease"],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2589384810?lang=zh_cn&edition=fundamental","pubTime":"2025-12-08 09:04","pubTimestamp":1765155840,"startTime":"0","endTime":"0","summary":"美国旧金山和中国苏州2025年12月8日 /美通社/ -- 信达生物制药集团,一家致力于研发、生产和销售肿瘤、自身免疫、代谢及心血管、眼科等重大疾病领域创新药物的生物制药公司,在2025年美国血液学会年会上以口头报告形式首次公布其自主开发的抗GPRC5D/BCMA/CD3三特异性抗体IBI3003用于复发或难治性多发性骨髓瘤患者的首次人体试验的初步数据。IBI3003的剂量优化研究正在积极推进中。我们也更为期待IBI3003持续治疗下长期随访的生存数据。","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":"https://wwwold.prnasia.com/story/archive/4840966_ZH40966_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":["LU0502904849.HKD","LU2097828557.USD","LU2097828474.EUR","ASH","LU2097828631.EUR","LU2328871848.SGD","01801","IVBIY","BK1161","HK0000165453.HKD","LU0455707207.USD","LU2463526074.USD","LU2097828714.EUR","BK4109","LU2097828805.USD","LU2242644610.SGD","LU2488822045.USD","LU1969619763.USD","BK1589","BK4139","BK1583"],"gpt_icon":0},{"id":"2589874964","title":"金斯瑞生物科技(01548):传奇宣布于2025年ASH年会上公布报告","url":"https://stock-news.laohu8.com/highlight/detail?id=2589874964","media":"智通财经","labels":["conferences"],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2589874964?lang=zh_cn&edition=fundamental","pubTime":"2025-12-07 19:04","pubTimestamp":1765105452,"startTime":"0","endTime":"0","summary":"智通财经APP讯,金斯瑞生物科技 发布公告,传奇生物科技股份有限公司于2025年12月6日发布新闻稿宣布于2025年美国血液学会年会上通过一项口头报告公布了CARVYKTI在复发或难治性多发性骨髓瘤患者中开展的CARTITUDE-1和CARTITUDE-4研究长期随访的临床及转化研究数据,以及III期研究CARTITUDE-4的最新结果,还通过六项壁报展示了CARVYKTI在不同亚组中的缓解持久性数据及真实世界研究结果。","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/1378515.html","is_publish_highlight":false,"source_rank":0,"column":"","sentiment":"0","news_top_title":null,"news_tag":"conferences","news_rank":0,"length":0,"strategy_id":0,"source":"stock_zhitongcaijing","symbols":["BK1583","BK1576","BK4109","BK1141","HK0000320223.HKD","01548","HK0000320264.USD","HK0000306685.HKD","HK0000306701.USD","LU2463526074.USD","ASH"],"gpt_icon":0},{"id":"2589871029","title":"维立志博-B(09887):LBL-034临床数据于第67届ASH年会发布","url":"https://stock-news.laohu8.com/highlight/detail?id=2589871029","media":"智通财经","labels":["dataReport"],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2589871029?lang=zh_cn&edition=fundamental","pubTime":"2025-12-07 18:28","pubTimestamp":1765103333,"startTime":"0","endTime":"0","summary":"智通财经APP讯,维立志博-B 发布公告,于2025年12月6日至9日,第67届ASH年会在美国佛罗里达州奥兰多召开。公司自主研发用于治疗复发性╱难治性多发性骨髓瘤的GPRC5D/CD3双特异性抗体LBL-034在大会首日第一个进行口头报告。LBL-034的主要临床亮点包括:LBL-034剂量递增至1,200μg/kg,未观察到任何剂量限制性毒性,未达到最大耐受剂量。与生活质量密切相关不良事件均为1至2级,多数不良事件发生于第一周期,在后续治疗中的发生率显著降低,不影响治疗连续性。","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/1378501.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":["HK0000500386.USD","HK0000252160.HKD","HK0000252152.HKD","LU2463526074.USD","BK1161","09887","BK4109","ASH"],"gpt_icon":1}],"pageSize":20,"totalPage":2,"pageCount":1,"totalSize":36,"code":"91000000","status":"200"}]}}