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Ultragenyx Pharmaceutical Inc

15.30

-0.1800-1.16%

盘前：15.20-0.1000-0.65%07:32 EDT

成交量：289.86万

成交额：4,426.93万

市值：15.04亿

市盈率：-2.63

高：15.49

开：15.42

低：15.10

收：15.48

52周最高：39.89

52周最低：12.73

股本：9,831.72万

流通股本：8,071.56万

量比：0.69

换手率：3.59%

股息：- -

股息率：- -

每股收益(TTM):-5.8279

每股收益(LYR):-5.8316

净资产收益率：-608.47%

总资产收益率：-24.22%

市净率：-5.17

市盈率(LYR):-2.62

数据加载中...

总览公司新闻资讯公告

Ultragenyx通过出售价值2.1亿美元的美国FDA凭证获利

Ultragenyx Pharmaceutical与美国卫生部达成协议，需将PRV销售收益的20%支付给NIH——SEC文件披露

Ultragenyx达成协议，将以2.1亿美元出售罕见儿科疾病优先审评券

Ultragenyx Pharmaceutical宣布其基因疗法Rebisufligene Etisparvovec的上市许可申请获欧洲药品管理局受理

异动解读｜Ultragenyx Pharmaceutical盘中上涨9.39%，FDA批准首款Sanfilippo综合征基因疗法持续提振股价

FDA批准治疗罕见病药物后，Ultragenyx股价上涨

Ultragenyx股票因里程碑式FDA批准而大涨

老虎资讯综合

Ultragenyx高管电话会议透露：Fayuvi在美国的每位患者批发采购成本定为395万美元

美国食品药品监督管理局（FDA）批准了Ultragenyx公司针对一种罕见疾病的基因疗法

Ionis Pharma将首款获FDA批准的亚历山大病治疗药物定价为每剂285,000美元

BUZZ——美国股市动态-黄金矿企、极星汽车、英伟达

美股盘前｜美债收益率回落，美股股指期货上涨；绩优股Snowflake盘前飙23%、Netskope涨12%，博通绩后跌超3%、维多利亚的秘密跌逾17%

老虎资讯综合

Ultragenyx Pharma股价暴跌，因罕见病药物临床试验失败

Ultragenyx Pharmaceutical治疗罕见病Angelman综合征的药物在后期试验中失败

老虎资讯综合

Ultragenyx的一款罕见病药物在后期临床试验中失败

Ultragenyx制药宣布评估Apazunersen项目并实施重大费用削减计划

Ultragenyx宣布Genglycos™（亦称DTX401）AAV基因疗法治疗GSD Ia的96周随机安慰剂对照交叉试验成功发表于《遗传代谢病杂志》

BUZZ——美国股市动态-苹果、Hims & Hers Health、Sysco

BUZZ——美国股市行情动态-诺德森、内比乌斯、迪尔

Ultragenyx罕见代谢病基因疗法获FDA批准，盘前股价飙升8.6%

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Inc.已签订协议，将出售其罕见儿科疾病优先审评券，交易金额达2.1亿美元。","market":"us","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":"1","news_top_title":null,"news_tag":"shareholding","news_rank":0,"length":0,"strategy_id":0,"source":null,"symbols":["RARE","BK4139"],"isVideo":false,"video":null,"gpt_icon":0},{"id":"1145307306","title":"Ultragenyx Pharmaceutical宣布其基因疗法Rebisufligene Etisparvovec的上市许可申请获欧洲药品管理局受理","url":"https://stock-news.laohu8.com/highlight/detail?id=1145307306","media":"美股速递","labels":["productRelease"],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/1145307306?lang=zh_cn&edition=fundamental","pubTime":"2026-10-02 14:04","pubTimestamp":1790921049,"startTime":"0","endTime":"0","summary":"Ultragenyx Pharmaceutical Inc（简称Ultragenyx Pharmaceutical）今日宣布，其针对Rebisufligene Etisparvovec基因疗法的上市许可申请（MAA）已通过欧洲药品管理局（EMA）的验证。","market":"us","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":"1","news_top_title":null,"news_tag":"productRelease","news_rank":0,"length":0,"strategy_id":0,"source":null,"symbols":["RARE","BK4139"],"isVideo":false,"video":null,"gpt_icon":0},{"id":"1115884749","title":"异动解读｜Ultragenyx Pharmaceutical盘中上涨9.39%，FDA批准首款Sanfilippo综合征基因疗法持续提振股价","url":"https://stock-news.laohu8.com/highlight/detail?id=1115884749","media":"行情直击","labels":["productRelease"],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/1115884749?lang=zh_cn&edition=fundamental","pubTime":"2026-09-23 00:39","pubTimestamp":1790095164,"startTime":"0","endTime":"0","summary":"9月22日，Ultragenyx Pharmaceutical盘中上涨9.39%，报16.025美元/股，成交额6472.9万美元，延续此前FDA获批后的上行动能。消息面上，FDA于上周批准公司旗下基因疗法Fayuvi，用于治疗A型Sanfilippo综合征儿童患者，系该适应症首个获批疗法。Fayuvi通过一次性静脉输注递送功能性基因，临床试验显示2至5岁患儿认知能力获得维持或改善。该药每位患者批发采购成本定为395万美元，为公司第六项FDA批准及第二款获批基因疗法。","market":"us","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":"2","news_top_title":"Ultragenyx盘中上涨，首款Sanfilippo基因疗法获批提振","news_tag":"productRelease","news_rank":0,"length":0,"strategy_id":0,"source":null,"symbols":["RARE"],"isVideo":false,"video":null,"gpt_icon":0},{"id":"2668923933","title":"FDA批准治疗罕见病药物后，Ultragenyx股价上涨","url":"https://stock-news.laohu8.com/highlight/detail?id=2668923933","media":"路透中文","labels":[],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2668923933?lang=zh_cn&edition=fundamental","pubTime":"2026-09-18 20:02","pubTimestamp":1789732921,"startTime":"0","endTime":"0","summary":"BUZZ-FDA批准治疗罕见病药物后，Ultragenyx股价上涨9月18日-** 制药公司Ultragenyx Pharmaceutical（RARE.O）的股价在盘前交易中上涨1%，至14.65美元，此前该公司周四收盘上涨12.58%** 美国食品和药物管理局（FDA）于周四晚间 (link) 批准了Ultragenyx的基因疗法Fayuvi，将其作为首款用于治疗A型桑菲利波综合征儿童的疗法*","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://api.refinitiv.com/data/news/v1/stories/urn:newsml:reuters.com:20260918:nL4S45A11L:1","is_publish_highlight":false,"source_rank":0,"column":"","sentiment":"2","news_top_title":null,"news_tag":"","news_rank":0,"length":0,"strategy_id":0,"source":null,"symbols":["RARE","BK4139","ABEO"],"isVideo":false,"video":null,"gpt_icon":0},{"id":"1113158668","title":"Ultragenyx股票因里程碑式FDA批准而大涨","url":"https://stock-news.laohu8.com/highlight/detail?id=1113158668","media":"老虎资讯综合","labels":["productRelease"],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/1113158668?lang=zh_cn&edition=fundamental","pubTime":"2026-09-18 10:25","pubTimestamp":1789698334,"startTime":"0","endTime":"0","summary":"消息公布后，Ultragenyx股价上涨。Ultragenyx股价周四大幅上涨，此前美国食品药品监督管理局批准了一种首创治疗方法，用于治疗患有罕见神经发育疾病的儿童患者。周四，Ultragenyx股价收涨13%，报14.50美元。FDA此次批准基于最长达8年的临床试验数据。Ultragenyx将在未来几天内推出一个网站，列出获得授权的治疗地点，并预计在30至60天内向这些治疗中心发货。Fayuvi是Ultragenyx获得批准的第二款基因疗法，也是该公司获得的第六项FDA批准。","market":"us","thumbnail":"https://community-static.tradeup.com/news/d506e40a3e9ad81e00eae5900753f7d1","type":0,"news_type":0,"thumbnails":["https://community-static.tradeup.com/news/d506e40a3e9ad81e00eae5900753f7d1"],"rights":null,"property":[],"language":"zh","translate_title":"","themeId":null,"theme_name":"","theme_type":"","isJumpTheme":false,"source_url":"","is_publish_highlight":true,"source_rank":0,"column":"","sentiment":"2","news_top_title":"Ultragenyx股票因里程碑式FDA批准而大涨","news_tag":"productRelease","news_rank":0,"length":0,"strategy_id":0,"source":null,"symbols":["RARE"],"isVideo":false,"video":null,"gpt_icon":1},{"id":"1145317877","title":"Ultragenyx高管电话会议透露：Fayuvi在美国的每位患者批发采购成本定为395万美元","url":"https://stock-news.laohu8.com/highlight/detail?id=1145317877","media":"美股速递","labels":["dataReport"],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/1145317877?lang=zh_cn&edition=fundamental","pubTime":"2026-09-18 05:59","pubTimestamp":1789682352,"startTime":"0","endTime":"0","summary":"在近期的一场电话会议中，Ultragenyx Pharmaceutical高管披露了一项关键定价信息。据其所述，该公司旗下药物Fayuvi在美国市场的每位患者批发采购成本已正式设定为395万美元。值得注意的是，此价格点被明确表述为“批发采购成本”，而非终端零售价，这一定价机制在医药行业内具有特定的经济意义，它通常构成了供应链中各环节定价的基础。","market":"us","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":"dataReport","news_rank":0,"length":0,"strategy_id":0,"source":null,"symbols":["BK4139","RARE"],"isVideo":false,"video":null,"gpt_icon":0},{"id":"2668991772","title":"美国食品药品监督管理局（FDA）批准了Ultragenyx公司针对一种罕见疾病的基因疗法","url":"https://stock-news.laohu8.com/highlight/detail?id=2668991772","media":"路透中文","labels":["productRelease"],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2668991772?lang=zh_cn&edition=fundamental","pubTime":"2026-09-18 02:39","pubTimestamp":1789670394,"startTime":"0","endTime":"0","summary":"美国食品药品监督管理局（FDA）批准了Ultragenyx公司针对一种罕见疾病的基因疗法路透9月17日-美国食品药品监督管理局周四表示，已批准Ultragenyx公司的RARE.O基因疗法，用于治疗一种罕见的致命性疾病。","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://api.refinitiv.com/data/news/v1/stories/urn:newsml:reuters.com:20260917:nL4S4591KZ: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":null,"symbols":["RARE","BK4139"],"isVideo":false,"video":null,"gpt_icon":0},{"id":"2664801101","title":"Ionis Pharma将首款获FDA批准的亚历山大病治疗药物定价为每剂285,000美元","url":"https://stock-news.laohu8.com/highlight/detail?id=2664801101","media":"路透中文","labels":["productRelease"],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2664801101?lang=zh_cn&edition=fundamental","pubTime":"2026-09-04 04:27","pubTimestamp":1788467231,"startTime":"0","endTime":"0","summary":"更新版 3-Ionis Pharma将首款获FDA批准的亚历山大病治疗药物定价为每剂285,000美元更新9月3日的报道，在第1段补充了定价细节，在第5段补充了患者护理人员的评论，在第7-8段补充了分析师的评论；修改了发稿地Siddhi Mahatole/Christy Santhosh路透9月4日-Ionis Pharmaceuticals公司周五表示，其新获批的亚历山大病治疗药物每剂定价为28.5万美元。Ionis预计，该疗法的峰值销售额将超过1亿美元，并表示该药物将在未来几周内于美国上市。Ionis表示，公司将继续通过一项开放标签扩展试验对Zanvastro进行研究。","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://api.refinitiv.com/data/news/v1/stories/urn:newsml:reuters.com:20260903:nL4S44V1NM:1","is_publish_highlight":false,"source_rank":0,"column":"","sentiment":"2","news_top_title":null,"news_tag":"productRelease","news_rank":0,"length":0,"strategy_id":0,"source":null,"symbols":["RARE","BK4139","IONS"],"isVideo":false,"video":null,"gpt_icon":0},{"id":"2664785872","title":"BUZZ——美国股市动态-黄金矿企、极星汽车、英伟达","url":"https://stock-news.laohu8.com/highlight/detail?id=2664785872","media":"路透中文","labels":[],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2664785872?lang=zh_cn&edition=fundamental","pubTime":"2026-09-03 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ental","pubTime":"2026-09-03 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Pharma股价暴跌，因罕见病药物临床试验失败","url":"https://stock-news.laohu8.com/highlight/detail?id=2664204388","media":"路透中文","labels":["dataReport"],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2664204388?lang=zh_cn&edition=fundamental","pubTime":"2026-09-03 16:54","pubTimestamp":1788425693,"startTime":"0","endTime":"0","summary":"BUZZ-Ultragenyx Pharma股价暴跌，因罕见病药物临床试验失败9月3日-** Ultragenyx Pharmaceutical（RARE.O）股价在盘前交易中下跌45.5%，至14.4美元** 该公司研发的药物阿帕祖纳森（apazunersen） (link) 在针对安杰尔曼综合征（一种影响神经系统并导致儿童期大脑发育异常的疾病）的晚期临床试验中未能达到主要研究目标** 与安慰剂","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://api.refinitiv.com/data/news/v1/stories/urn:newsml:reuters.com:20260903:nL4T44V0N3:1","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":null,"symbols":["BK4139","IONS","RARE"],"isVideo":false,"video":null,"gpt_icon":0},{"id":"1124499300","title":"Ultragenyx Pharmaceutical治疗罕见病Angelman综合征的药物在后期试验中失败","url":"https://stock-news.laohu8.com/highlight/detail?id=1124499300","media":"老虎资讯综合","labels":["dataReport"],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/1124499300?lang=zh_cn&edition=fundamental","pubTime":"2026-09-03 16:34","pubTimestamp":1788424478,"startTime":"0","endTime":"0","summary":"生物技术公司  $Ultragenyx Pharmaceutical Inc$ 表示，其治疗Angelman综合征的实验性疗法在一项大型3期试验中与模拟治疗相比未显示出获益。该药物GTX-102在早期试验中曾显示出显著效果，给受这种毁灭性疾病影响的家庭带来了希望。这一消息对Ultragenyx的业务也是一个重大打击。尽管该公司有多种获批药物，但它们大多针对超罕见疾病，投资者一直指望这款Angelman综合征药物成为公司实现盈利的途径。","market":"us","thumbnail":"https://static.tigerbbs.com/85675909dc6c67ee0181339c18bcfdff","type":0,"news_type":0,"thumbnails":["https://static.tigerbbs.com/85675909dc6c67ee0181339c18bcfdff"],"rights":null,"property":[],"language":"zh","translate_title":"","themeId":null,"theme_name":"","theme_type":"","isJumpTheme":false,"source_url":"","is_publish_highlight":true,"source_rank":0,"column":"","sentiment":"-2","news_top_title":"Ultragenyx Pharmaceutical治疗罕见病Angelman综合征的药物在后期试验中失败","news_tag":"dataReport","news_rank":0,"length":0,"strategy_id":0,"source":null,"symbols":["RARE"],"isVideo":false,"video":null,"gpt_icon":0},{"id":"2664849377","title":"Ultragenyx的一款罕见病药物在后期临床试验中失败","url":"https://stock-news.laohu8.com/highlight/detail?id=2664849377","media":"路透中文","labels":["dataReport"],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2664849377?lang=zh_cn&edition=fundamental","pubTime":"2026-09-03 04:06","pubTimestamp":1788379577,"startTime":"0","endTime":"0","summary":"Ultragenyx的一款罕见病药物在后期临床试验中失败路透9月2日-Ultragenyx制药公司（RARE.O）周三表示，其用于治疗一种罕见遗传性神经发育障碍的试验性药物在后期临床试验中未达到主要目标。","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://api.refinitiv.com/data/news/v1/stories/urn:newsml:reuters.com:20260902:nL4S44U1TK:1","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":null,"symbols":["BK4139","RARE"],"isVideo":false,"video":null,"gpt_icon":0},{"id":"1162487658","title":"Ultragenyx制药宣布评估Apazunersen项目并实施重大费用削减计划","url":"https://stock-news.laohu8.com/highlight/detail?id=1162487658","media":"美股速递","labels":[],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/1162487658?lang=zh_cn&edition=fundamental","pubTime":"2026-09-03 04:03","pubTimestamp":1788379416,"startTime":"0","endTime":"0","summary":"Ultragenyx Pharmaceutical——这家专注于罕见病药物研发的生物制药公司，近日对外宣布，将对其Apazunersen项目进行全面评估，同时着手推行一系列意义深远的费用缩减措施。\n这一战略调整，无疑透露出公司在管线优化与资源分配上的深思熟虑。对于Apazunersen这一在研项目，公司显然意在通过严谨的审视，为其后续走向定夺方向。\n与此同时，费用削减计划的实施，也昭示着公司正在积极应对当前的经济环境，力求在研发投入与财务稳健之间寻求更为精准的平衡。此举或将对公司未来的运营格局产生重要影响。","market":"us","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":"-1","news_top_title":null,"news_tag":"","news_rank":0,"length":0,"strategy_id":0,"source":null,"symbols":["BK4139","RARE"],"isVideo":false,"video":null,"gpt_icon":0},{"id":"1192232987","title":"Ultragenyx宣布Genglycos™（亦称DTX401）AAV基因疗法治疗GSD Ia的96周随机安慰剂对照交叉试验成功发表于《遗传代谢病杂志》","url":"https://stock-news.laohu8.com/highlight/detail?id=1192232987","media":"美股速递","labels":["dataReport"],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/1192232987?lang=zh_cn&edition=fundamental","pubTime":"2026-09-02 04:07","pubTimestamp":1788293247,"startTime":"0","endTime":"0","summary":"Ultragenyx Pharmaceutical今日宣布，其针对Ia型糖原贮积病的AAV基因疗法Genglycos所开展的一项长达96周的随机、安慰剂对照、交叉设计临床试验，其研究成果已正式发表于权威期刊《遗传代谢病杂志》。该项研究历时近两年，采用严谨的双盲、随机、安慰剂对照方法，并在后期阶段引入交叉治疗设计，旨在全面评估Genglycos在GSD Ia患者群体中的疗效与安全性。","market":"us","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":"1","news_top_title":null,"news_tag":"dataReport","news_rank":0,"length":0,"strategy_id":0,"source":null,"symbols":["BK4139","RARE"],"isVideo":false,"video":null,"gpt_icon":0},{"id":"2660235572","title":"BUZZ——美国股市动态-苹果、Hims & Hers Health、Sysco","url":"https://stock-news.laohu8.com/highlight/detail?id=2660235572","media":"路透中文","labels":["dataReport"],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2660235572?lang=zh_cn&edition=fundamental","pubTime":"2026-08-20 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19:04","pubTimestamp":1787223856,"startTime":"0","endTime":"0","summary":"Ultragenyx Pharmaceutical（股票代码：RARE）周三盘前交易时段股价大幅攀升8.6%，此前该公司宣布其针对罕见代谢紊乱的基因疗法已获得美国食品药品监督管理局（FDA）的正式批准。这一里程碑式的进展，无疑为这家生物制药公司注入了强劲的市场信心。该疗法专门用于治疗一种罕见的遗传性代谢疾病，为长期缺乏有效治疗方案的患者群体带来了新的希望。市场对此消息反应热烈，投资者情绪高涨，推动股价在常规交易开始前即出现显著上涨。分析人士指出，此次获批不仅有望为Ultragenyx打开新的收入渠道，也可能巩固其在基因治疗细分领域的领先地位。","market":"us","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":"2","news_top_title":null,"news_tag":"productRelease","news_rank":0,"length":0,"strategy_id":0,"source":null,"symbols":["RARE","BK4139"],"isVideo":false,"video":null,"gpt_icon":0}],"pageSize":20,"totalPage":2,"pageCount":1,"totalSize":28,"code":"91000000","status":"200"}]}}