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BIIB 渤健公司
未开盘 07-19 16:00:00 EDT
226.40
+1.15
+0.51%
盘后
226.40
+0.00
0.00%
19:16 EDT
最高
227.63
最低
222.38
成交量
85.18万
今开
225.67
昨收
225.25
日振幅
2.33%
总市值
329.63亿
流通市值
328.48亿
总股本
1.46亿
成交额
1.92亿
换手率
0.59%
流通股本
1.45亿
市净率
--
ROE
--
每股收益
0.00
52周最高
--
52周最低
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市盈率
--
股息
--
股息收益率
--
ROA
--
分时
五日
日K
周K
月K
北京优虎网络科技有限公司
资讯
新帖
简况
诺和诺德支持瑞士生物技术公司 Asceneuron 完成 1 亿美元融资
Reuters · 07-16
诺和诺德支持瑞士生物技术公司 Asceneuron 完成 1 亿美元融资
BUZZ--美国股票走势-特斯拉、泰克资源、摩根大通
Reuters · 07-12
BUZZ--美国股票走势-特斯拉、泰克资源、摩根大通
BUZZ-派珀-桑德勒下调百健公司的目标价,预计阿尔茨海默氏症药物Leqembi的接受度不高
Reuters · 07-12
BUZZ-派珀-桑德勒下调百健公司的目标价,预计阿尔茨海默氏症药物Leqembi的接受度不高
BMO:礼来(LLY.US)阿尔茨海默氏症药有望创收71亿美元 优于渤健(BIIB.US)竞品
智通财经 · 07-04
BMO:礼来(LLY.US)阿尔茨海默氏症药有望创收71亿美元 优于渤健(BIIB.US)竞品
背景资料-礼来紧随百健-艾赛之后,获得美国食品及药物管理局对阿尔茨海默氏症药物的批准
Reuters · 07-03
背景资料-礼来紧随百健-艾赛之后,获得美国食品及药物管理局对阿尔茨海默氏症药物的批准
BUZZ-券商观点:礼来的阿尔茨海默氏症药物获批也可能使百健受益
Reuters · 07-03
BUZZ-券商观点:礼来的阿尔茨海默氏症药物获批也可能使百健受益
礼来(LLY.US)阿尔茨海默氏症药获美国FDA批准 与渤健(BIIB.US)展开两强争霸!
智通财经 · 07-03
礼来(LLY.US)阿尔茨海默氏症药获美国FDA批准 与渤健(BIIB.US)展开两强争霸!
卫材与百健联合在中国推出阿尔茨海默氏症药物乐清碧
Reuters · 06-28
卫材与百健联合在中国推出阿尔茨海默氏症药物乐清碧
媒体-百健下一步并购赌注高达 100 亿美元--彭博新闻社
Reuters · 06-26
媒体-百健下一步并购赌注高达 100 亿美元--彭博新闻社
更新 5-礼来阿尔茨海默氏症药物获得 FDA 顾问小组一致支持
Reuters · 06-11
更新 5-礼来阿尔茨海默氏症药物获得 FDA 顾问小组一致支持
美国食品和药物管理局顾问将审查礼来公司的阿尔茨海默氏症药物
Reuters · 06-10
美国食品和药物管理局顾问将审查礼来公司的阿尔茨海默氏症药物
更新版 1-美国 FDA 专家小组将就礼来老年痴呆症药物的数据和安全性进行投票表决
Reuters · 06-06
更新版 1-美国 FDA 专家小组将就礼来老年痴呆症药物的数据和安全性进行投票表决
欧盟执委会批准百健公司 ALS 药物上市
Reuters · 05-31
欧盟执委会批准百健公司 ALS 药物上市
加拿大皇家银行:重申Biogen(BIIB.US)评级,由优于大市调整至优于大市评级, 目标价317.00美元。
智通财经 · 05-29
加拿大皇家银行:重申Biogen(BIIB.US)评级,由优于大市调整至优于大市评级, 目标价317.00美元。
卫材(ESALY.US)/渤健(BIIB.US)阿尔茨海默病抗体新药在韩国获批上市
智通财经 · 05-28
卫材(ESALY.US)/渤健(BIIB.US)阿尔茨海默病抗体新药在韩国获批上市
Biogen Inc-在韩国卫材韩国公司将分销产品并开展信息提供活动
智通财经 · 05-27
Biogen Inc-在韩国卫材韩国公司将分销产品并开展信息提供活动
HC Wainwright & Co.:重申Biogen(BIIB.US)评级,由买入调整至买入评级, 目标价300.00美元。
智通财经 · 05-23
HC Wainwright & Co.:重申Biogen(BIIB.US)评级,由买入调整至买入评级, 目标价300.00美元。
百健(BIIB.US)将以18亿美元收购免疫药物开发商 HI-Bio
智通财经 · 05-22
百健(BIIB.US)将以18亿美元收购免疫药物开发商 HI-Bio
更新版 1-百健公司将以最高 18 亿美元收购人类免疫学生物科学公司
Reuters · 05-22
更新版 1-百健公司将以最高 18 亿美元收购人类免疫学生物科学公司
Biogen Inc-Biogen预计将用现金为收购融资还可能利用其循环信贷协议
智通财经 · 05-22
Biogen Inc-Biogen预计将用现金为收购融资还可能利用其循环信贷协议
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公司概况
公司名称:
渤健公司
所属市场:
NASDAQ
上市日期:
--
主营业务:
Biogen Inc.于1985年在加利福尼亚州以IDEC制药公司的名义成立,并于1997年重新注册为特拉华州公司。2003年,他们收购了Biogen, Inc.,并将公司名称更改为Biogen Idec Inc.。该公司是一家全球性的生物制药公司,专注于为患有严重神经和神经退行性疾病的患者以及相关的治疗邻接患者发现、开发和提供全球创新疗法。该公司的核心增长领域包括多发性硬化症(MS)和神经免疫学;阿尔茨海默病(AD)和痴呆症;神经肌肉疾病,包括脊髓肌萎缩症(SMA)和肌萎缩侧索硬化症(ALS);运动障碍,包括帕金森氏症;以及眼科学。该公司还专注于在免疫学、神经认知障碍、急性神经学和疼痛等新兴增长领域发现、开发和提供全球创新疗法。
发行价格:
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18:55","pubTimestamp":1720781735,"startTime":"0","endTime":"0","summary":" 7月12日 - ** 券商Piper Sandler将百健 的股票交易价格从335美元下调至313美元,同时下调了该公司阿尔茨海默病 药物Leqembi的近期和长期销售前景。** 经纪公司称,虽然准入限制有所放宽,但医生们仍对安全性、输液物流以及该药物的预期疗效表示担忧。** 现将 Leqembi 公司 24 年第二季度的营业额预测从 490 万美元下调至 3000 万美元,并下调了第三季度和第四季度的预测。","market":"us","thumbnail":null,"type":0,"news_type":0,"thumbnails":[],"rights":null,"property":["rate"],"language":"zh","translate_title":"","themeId":null,"isJumpTheme":false,"source_url":"https://api.rkd.refinitiv.com/api/News/News.svc/REST/News_1/RetrieveStoryML_1","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":["BIIB","LLY","BUZZ"],"gpt_icon":0},{"id":"2448449335","title":"BMO:礼来(LLY.US)阿尔茨海默氏症药有望创收71亿美元 优于渤健(BIIB.US)竞品","url":"https://stock-news.laohu8.com/highlight/detail?id=2448449335","media":"智通财经","labels":[],"top":-1,"share":"https://www.laohu8.com/m/news/2448449335?lang=zh_cn&edition=full","pubTime":"2024-07-04 11:59","pubTimestamp":1720065555,"startTime":"0","endTime":"0","summary":"智通财经获悉,据BMO报道,礼来公司 最新获批准的阿尔茨海默病药物donanemab可能为该公司带来高达71亿美元的峰值销售额,并将有助于该制药商的收入来源多样化。礼来公司表示,符合条件的患者可以获得医疗保险覆盖和报销。该药物预计将与日本卫材医药和渤健的同类药物Leqembi竞争,Leqembi于2023年获得FDA批准。礼来公司的乳腺癌药物Verzenio以39亿美元的销售额位居第三。礼来2023年的总收入为340亿美元。","market":"hk","thumbnail":null,"type":0,"news_type":0,"thumbnails":[],"rights":null,"property":[],"language":"zh","translate_title":"","themeId":null,"isJumpTheme":false,"source_url":"http://www.zhitongcaijing.com/content/detail/1145468.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":["IE0002141913.USD","IE00B1BXHZ80.USD","LU2237443622.USD","LU0114720955.EUR","LU2237443978.SGD","LU1804176565.USD","LU0079474960.USD","LU0417517546.SGD","LU2237443382.USD","LU0943347566.SGD","BK4534","LU0238689110.USD","LU2491050071.SGD","BK4007","IE00B19Z9P08.USD","IE00BJJMRZ35.SGD","LU1057294990.SGD","LU0234570918.USD","LU1023059063.AUD","LU0708995401.HKD","BK4581","BK4533","LU0058720904.USD","BMO","LU0061475181.USD","LU0320765992.SGD","IE00B19Z9Z06.USD","IE00B894F039.SGD","LLY","LU1551013342.USD","LU1551013425.SGD","LU0256863811.USD","LU2237443549.SGD","LU2468319806.SGD","LU0122379950.USD","BK4532","LU1814569148.SGD","LU2264538146.SGD","IE0004445239.USD","GB00BDT5M118.USD","LU1988902786.USD","LU0289739699.SGD","LU1280957306.USD","LU2491049909.HKD","LU0882574055.USD","IE00BJT1NW94.SGD","LU0672654240.SGD","BIIB","LU2237438978.USD","LU0109391861.USD"],"gpt_icon":0},{"id":"2448104359","title":"背景资料-礼来紧随百健-艾赛之后,获得美国食品及药物管理局对阿尔茨海默氏症药物的批准","url":"https://stock-news.laohu8.com/highlight/detail?id=2448104359","media":"Reuters","labels":[],"top":-1,"share":"https://www.laohu8.com/m/news/2448104359?lang=zh_cn&edition=full","pubTime":"2024-07-03 20:18","pubTimestamp":1720009106,"startTime":"0","endTime":"0","summary":" 路透7月3日 - 礼来公司 的Kisunla周二获得了美国食品和药物管理局的标准批准,用于减缓阿尔茨海默氏症的进展。Kisunla是继百健 和日本卫材 的Leqembi之后,第二种获得美国监管机构传统批准的治疗脑萎缩疾病的药物,这在一个经历了多次失败的领域是一个重要的里程碑。","market":"us","thumbnail":null,"type":0,"news_type":0,"thumbnails":[],"rights":null,"property":[],"language":"zh","translate_title":"","themeId":null,"isJumpTheme":false,"source_url":"https://api.rkd.refinitiv.com/api/News/News.svc/REST/News_1/RetrieveStoryML_1","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":["LU0289739699.SGD","LU1814569148.SGD","LU0708995401.HKD","IE0004445239.USD","ACW.AU","BIIB","IE00B19Z9P08.USD","LU0061475181.USD","BK4007","CGTX","LU2491049909.HKD","LGVN","LU0122379950.USD","LU1988902786.USD","ACIU","IE00B894F039.SGD","GB00BDT5M118.USD","LU1057294990.SGD","LU0256863811.USD","ANVS","LU1551013425.SGD","LLY","BK4533","LU1023059063.AUD","IE00BJJMRZ35.SGD","LU1804176565.USD","LU0058720904.USD","LU2237443978.SGD","LU2264538146.SGD","BK4534","IE00BJT1NW94.SGD","BIVI","LU2237438978.USD","COYA","LU2237443549.SGD","LU2237443382.USD","LU0320765992.SGD","IE00B1BXHZ80.USD","LU0079474960.USD","IE0002141913.USD","LU0882574055.USD","LU2468319806.SGD","LU2491050071.SGD","BK4532","LU1280957306.USD","LU2237443622.USD","LU0109391861.USD","LU1551013342.USD","BK7067","LU0943347566.SGD"],"gpt_icon":0},{"id":"2448773691","title":"BUZZ-券商观点:礼来的阿尔茨海默氏症药物获批也可能使百健受益","url":"https://stock-news.laohu8.com/highlight/detail?id=2448773691","media":"Reuters","labels":[],"top":-1,"share":"https://www.laohu8.com/m/news/2448773691?lang=zh_cn&edition=full","pubTime":"2024-07-03 18:02","pubTimestamp":1720000945,"startTime":"0","endTime":"0","summary":" 7月3日 - ** 美国食品和药物管理局周二批准了 礼来公司的 治疗早期阿尔茨海默氏症的药物,该药物的品牌名称为Kisunla,这是将向美国患者提供的第二种减缓这种脑损伤疾病进展的疗法。** BMO Capital Markets 称,预计 Kisunla 的销售峰值将达到 71 亿美元,这将使该公司在本十年后半期的收入实现多样化。** Truist Securities 称,Kisunla的差异化特征有可能降低总体治疗成本。","market":"us","thumbnail":null,"type":0,"news_type":0,"thumbnails":[],"rights":null,"property":[],"language":"zh","translate_title":"","themeId":null,"isJumpTheme":false,"source_url":"https://api.rkd.refinitiv.com/api/News/News.svc/REST/News_1/RetrieveStoryML_1","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":["LU0234570918.USD","LU0672654240.SGD","LU1804176565.USD","LU2491050071.SGD","LU0882574055.USD","LU0943347566.SGD","LU0061475181.USD","LU2237438978.USD","LLY","LU2237443549.SGD","LU1551013342.USD","IE00B894F039.SGD","IE00BJJMRZ35.SGD","IE00B19Z9P08.USD","LU0079474960.USD","LU0122379950.USD","LU0114720955.EUR","LU2237443622.USD","LU2468319806.SGD","BK4533","LU0109391861.USD","IE0004445239.USD","IE00B1BXHZ80.USD","LU1988902786.USD","LU0417517546.SGD","BK4007","LU2237443978.SGD","BK4581","LU0058720904.USD","IE0002141913.USD","IE00B19Z9Z06.USD","BK4532","LU0708995401.HKD","LU1023059063.AUD","LU1057294990.SGD","LU1551013425.SGD","LU1814569148.SGD","LU2237443382.USD","BUZZ","LU2491049909.HKD","LU0256863811.USD","IE00BJT1NW94.SGD","GB00BDT5M118.USD","LU0320765992.SGD","LU0289739699.SGD","BIIB","LU1280957306.USD","BK4534","LU2264538146.SGD","LU0238689110.USD"],"gpt_icon":0},{"id":"2448119882","title":"礼来(LLY.US)阿尔茨海默氏症药获美国FDA批准 与渤健(BIIB.US)展开两强争霸!","url":"https://stock-news.laohu8.com/highlight/detail?id=2448119882","media":"智通财经","labels":[],"top":-1,"share":"https://www.laohu8.com/m/news/2448119882?lang=zh_cn&edition=full","pubTime":"2024-07-03 08:06","pubTimestamp":1719965170,"startTime":"0","endTime":"0","summary":"智通财经获悉,礼来研发的药物“donanemab-azbt”被美国食品和药物管理局批准用于治疗有轻度认知障碍的阿尔茨海默病早期患者,商品名为“Kisunla”。根据阿尔茨海默病协会的数据,近700万美国人患有这种疾病,是65岁以上老年人的第五大死因。“双雄争霸”阿尔茨海默病治疗领域Donanemab将与渤健及其日本合作伙伴卫材药业的另一种治疗药物Leqembi展开正面竞争。FDA因在2021年加速批准Aduhelm而受到批评,尽管咨询小组提出了负面建议。","market":"us","thumbnail":null,"type":0,"news_type":0,"thumbnails":[],"rights":null,"property":[],"language":"zh","translate_title":"","themeId":null,"isJumpTheme":false,"source_url":"http://www.zhitongcaijing.com/content/detail/1144820.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":["BK4534","LU1551013342.USD","LU1623119135.USD","LU1814569148.SGD","LU2237443549.SGD","LU0122379950.USD","LU2237443382.USD","LU0256863811.USD","LU2264538146.SGD","IE00BJT1NW94.SGD","BK4532","LU1551013425.SGD","IE00BJJMRZ35.SGD","LU2468319806.SGD","LU2491049909.HKD","LU1988902786.USD","LU0385154629.USD","LU0097036916.USD","LU0061475181.USD","LU2491050071.SGD","IE0002141913.USD","LU0289739699.SGD","LU1804176565.USD","BK4533","LU2237443978.SGD","LU0708995401.HKD","LU1023059063.AUD","LU1280957306.USD","LU1712237335.SGD","LU2265009873.SGD","LU0943347566.SGD","IE00B1BXHZ80.USD","BIIB","IE00B894F039.SGD","GB00BDT5M118.USD","LU0689472784.USD","LU1057294990.SGD","IE0009355771.USD","LU0820561909.HKD","LU0114720955.EUR","BK4007","IE00B19Z9P08.USD","LU2237443622.USD","LU0079474960.USD","LU0320765992.SGD","LU0882574055.USD","LU0058720904.USD","LLY","LU0109391861.USD","IE0004445239.USD"],"gpt_icon":0},{"id":"2446513977","title":"卫材与百健联合在中国推出阿尔茨海默氏症药物乐清碧","url":"https://stock-news.laohu8.com/highlight/detail?id=2446513977","media":"Reuters","labels":[],"top":-1,"share":"https://www.laohu8.com/m/news/2446513977?lang=zh_cn&edition=full","pubTime":"2024-06-28 08:48","pubTimestamp":1719535689,"startTime":"0","endTime":"0","summary":" 路透6月28日 - 卫材 和百健 周五表示,它们已在中国推出阿尔茨海默氏症治疗药物Leqembi,中国是继美国和日本之后的第三个国家。Leqembi通过清除大脑中一种叫做β淀粉样蛋白的有毒蛋白质而发挥作用,它是第一种被证实能改变这种致命性脑损伤疾病病程的阿尔茨海默氏症治疗药物。卫材公司还与中国一家大型医疗保险公司合作,计划承担部分药费,但未透露保险公司名称。","market":"us","thumbnail":null,"type":0,"news_type":0,"thumbnails":[],"rights":null,"property":[],"language":"zh","translate_title":"","themeId":null,"isJumpTheme":false,"source_url":"https://api.rkd.refinitiv.com/api/News/News.svc/REST/News_1/RetrieveStoryML_1","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":["BIIB","BK4533","BK4139","IE00B19Z9P08.USD","LU0109394709.USD","IE00B19Z9Z06.USD","BK4585","BK4532","LU0234570918.USD","IE00B894F039.SGD","LU0889565916.HKD","LU0320765992.SGD","BK4588"],"gpt_icon":0},{"id":"2446111826","title":"媒体-百健下一步并购赌注高达 100 亿美元--彭博新闻社","url":"https://stock-news.laohu8.com/highlight/detail?id=2446111826","media":"Reuters","labels":[],"top":-1,"share":"https://www.laohu8.com/m/news/2446111826?lang=zh_cn&edition=full","pubTime":"2024-06-26 00:19","pubTimestamp":1719332399,"startTime":"0","endTime":"0","summary":"((自动化翻译由路透提供,请见免责声明 )) 6月25日 - -- 来源链接: -- 注:路透未核实此报道,不保证其准确性","market":"us","thumbnail":null,"type":0,"news_type":0,"thumbnails":[],"rights":null,"property":[],"language":"zh","translate_title":"","themeId":null,"isJumpTheme":false,"source_url":"https://api.rkd.refinitiv.com/api/News/News.svc/REST/News_1/RetrieveStoryML_1","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":["BK4532","LU0320765992.SGD","BK4585","BK4533","LU0889565916.HKD","IE00B19Z9Z06.USD","BIIB","BK4139","IE00B19Z9P08.USD","LU0109394709.USD","IE00B894F039.SGD","BK4588","LU0234570918.USD"],"gpt_icon":0},{"id":"2442587286","title":"更新 5-礼来阿尔茨海默氏症药物获得 FDA 顾问小组一致支持","url":"https://stock-news.laohu8.com/highlight/detail?id=2442587286","media":"Reuters","labels":[],"top":-1,"share":"https://www.laohu8.com/m/news/2442587286?lang=zh_cn&edition=full","pubTime":"2024-06-11 05:48","pubTimestamp":1718056097,"startTime":"0","endTime":"0","summary":"几位专家组成员指出,对于有两个 APOE4 基因拷贝的人来说,安全问题更为突出,因为这种基因拷贝与更高的阿尔茨海默氏症风险有关。礼来公司说,它正计划在有阿尔茨海默氏症遗传倾向的患者中进行试验,测试这种治疗方法。","market":"us","thumbnail":null,"type":0,"news_type":0,"thumbnails":[],"rights":null,"property":[],"language":"zh","translate_title":"","themeId":null,"isJumpTheme":false,"source_url":"https://api.rkd.refinitiv.com/api/News/News.svc/REST/News_1/RetrieveStoryML_1","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":["LU1023059063.AUD","BK4534","LU0943347566.SGD","LU2237443622.USD","LU1267930730.SGD","LU1988902786.USD","BIIB","LU0640476718.USD","LU1057294990.SGD","BK4588","LU2237443382.USD","LU2491050071.SGD","IE0002141913.USD","IE0004445239.USD","LU1804176565.USD","IE00B1BXHZ80.USD","BK4007","IE00B19Z9Z06.USD","IE00BJT1NW94.SGD","LU0238689110.USD","LU0708995401.HKD","LU0882574139.USD","GB00BDT5M118.USD","IE00B2B36J28.USD","LU0320765059.SGD","LU1551013342.USD","LU2237438978.USD","LU0820561818.USD","IE00B19Z9P08.USD","BK4532","LU0058720904.USD","BK4581","BK4533","LU0289739699.SGD","LU1712237335.SGD","LU2468319806.SGD","LU0234570918.USD","LU0109394709.USD","LU1064131342.USD","LU0889565916.HKD","LLY","LU0097036916.USD","LU0256863811.USD","LU2264538146.SGD","IE00BFTCPJ56.SGD","BK4139","LU2237443978.SGD","LU2265009873.SGD","LU2491049909.HKD","LU0122379950.USD"],"gpt_icon":1},{"id":"2442284834","title":"美国食品和药物管理局顾问将审查礼来公司的阿尔茨海默氏症药物","url":"https://stock-news.laohu8.com/highlight/detail?id=2442284834","media":"Reuters","labels":[],"top":-1,"share":"https://www.laohu8.com/m/news/2442284834?lang=zh_cn&edition=full","pubTime":"2024-06-10 19:00","pubTimestamp":1718017235,"startTime":"0","endTime":"0","summary":" Bhanvi Satija/Julie Steenhuysen 路透6月10日 - 美国食品和药物管理局的一个独立顾问小组将于周一晚些时候就礼来公司 的阿尔茨海默氏症试验性药物多奈单抗的安全性和有效性进行投票表决。礼来公司的这种药物和其他同类药物可能导致致命的脑肿胀或脑出血。至少有四位华尔街分析师上周表示,美国食品及药物管理局的审查人员 ,没有提出任何严重的警示,他们预计donanemab将获得批准。据阿尔茨海默氏症协会称,超过 600 万美国人患有某种形式的破坏记忆的疾病。","market":"us","thumbnail":null,"type":0,"news_type":0,"thumbnails":[],"rights":null,"property":[],"language":"zh","translate_title":"","themeId":null,"isJumpTheme":false,"source_url":"https://api.rkd.refinitiv.com/api/News/News.svc/REST/News_1/RetrieveStoryML_1","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":["LU0079474960.USD","IE0002141913.USD","IE00B19Z9P08.USD","IE00B1BXHZ80.USD","LU0320765992.SGD","LU1804176565.USD","LU1551013342.USD","LU1551013425.SGD","LU0061475181.USD","LLY","LU2237443549.SGD","LU2468319806.SGD","LU2491049909.HKD","LU2491050071.SGD","LU2491050154.USD","LU1023059063.AUD","LU0234570918.USD","LU0256863811.USD","BK4007","LU0289739699.SGD","LU2264538146.SGD","LU0238689110.USD","GB00BDT5M118.USD","LU1057294990.SGD","BK4532","LU0114720955.EUR","IE0004445239.USD","LU0708995401.HKD","BK4534","LU2237438978.USD","BIIB","LU2237443382.USD","LU1988902786.USD","IE00BJT1NW94.SGD","IE00B894F039.SGD","LU2237443978.SGD","LU0122379950.USD","LU0943347566.SGD","BK4533","IE00BJJMRZ35.SGD","LU0417517546.SGD","LU1280957306.USD","LU2237443622.USD","BK4581","LU0672654240.SGD","LU0058720904.USD","LU0882574055.USD","LU1814569148.SGD","LU0109391861.USD","IE00B19Z9Z06.USD"],"gpt_icon":0},{"id":"2441710171","title":"更新版 1-美国 FDA 专家小组将就礼来老年痴呆症药物的数据和安全性进行投票表决","url":"https://stock-news.laohu8.com/highlight/detail?id=2441710171","media":"Reuters","labels":[],"top":-1,"share":"https://www.laohu8.com/m/news/2441710171?lang=zh_cn&edition=full","pubTime":"2024-06-06 21:56","pubTimestamp":1717682196,"startTime":"0","endTime":"0","summary":" 路透6月6日 - 美国卫生监管机构的一个外部专家小组将于周一召开会议,就礼来 的多那单抗的安全性和疗效数据进行投票,并向FDA提出建议,该药是卫材 和百健 的Leqembi的潜在竞争对手。该机构网站周四公布的文件显示,该小组还将就治疗的益处是否大于风险进行投票。阿尔茨海默氏症试验曾发现该类药物存在脑肿胀和出血等安全隐患。在礼来公司的试验中,有三名参与者死于与治疗有关的并发症。","market":"us","thumbnail":null,"type":0,"news_type":0,"thumbnails":[],"rights":null,"property":[],"language":"zh","translate_title":"","themeId":null,"isJumpTheme":false,"source_url":"https://api.rkd.refinitiv.com/api/News/News.svc/REST/News_1/RetrieveStoryML_1","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":["BK4588","LU0114720955.EUR","LU0097036916.USD","LU2491049909.HKD","BK4007","LU0943347566.SGD","LU1280957306.USD","BK4534","LU0289739699.SGD","LU0320765992.SGD","LU0058720904.USD","IE0002141913.USD","LU1988902786.USD","LU2237443978.SGD","LU2264538146.SGD","LU1712237335.SGD","LU2491050154.USD","BK4533","IE00BJT1NW94.SGD","LU0122379950.USD","LU0708995401.HKD","LU2491050071.SGD","IE0004445239.USD","LU1623119135.USD","IE00B1BXHZ80.USD","IE0009355771.USD","LU1551013342.USD","LU1814569148.SGD","LU1023059063.AUD","LLY","LU0882574055.USD","LU2237443622.USD","IE00BJJMRZ35.SGD","LU1551013425.SGD","GB00BDT5M118.USD","IE00B19Z9P08.USD","LU2237443382.USD","BK4581","LU1804176565.USD","LU2237443549.SGD","LU0061475181.USD","LU0109391861.USD","BIIB","LU0256863811.USD","IE00B894F039.SGD","BK4532","LU1057294990.SGD","LU2468319806.SGD","LU0820561909.HKD","LU0079474960.USD"],"gpt_icon":0},{"id":"2439601669","title":"欧盟执委会批准百健公司 ALS 药物上市","url":"https://stock-news.laohu8.com/highlight/detail?id=2439601669","media":"Reuters","labels":[],"top":-1,"share":"https://www.laohu8.com/m/news/2439601669?lang=zh_cn&edition=full","pubTime":"2024-05-31 06:04","pubTimestamp":1717106694,"startTime":"0","endTime":"0","summary":"((自动化翻译由路透提供,请见免责声明 )) 路透5月30日 - 百健 周四称,欧盟执委会在特殊情况下批准了其肌萎缩性脊髓侧索硬化症(ALS) 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