Ultragenyx Pharmaceutical Inc(RARE)_个股概要_股票价格_最新资讯_行情走势_历史数据 - 老虎社区

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RARE Ultragenyx Pharmaceutical Inc

未开盘 06-29 16:00:00 EDT

30.68

-0.09

-0.29%

盘后31.28

+0.60+1.96%

19:51 EDT

最高31.16	最低30.19	成交量399.52万
今开30.77	昨收30.77	日振幅3.15%
总市值30.16亿	流通市值28.99亿	总股本9,832万
成交额1.23亿	换手率4.23%	流通股本9,449万
市净率--	ROE--	每股收益0.00
52周最高--	52周最低--	市盈率--
股息--	股息收益率--	ROA--

数据加载中...

北京优虎网络科技有限公司

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Biotherapeutics任命前基因泰克/罗氏与Celgene高管Corsee Sanders博士加入董事会","url":"https://stock-news.laohu8.com/highlight/detail?id=1154584198","media":"美股速递","labels":["executive"],"top":-1,"itemType":null,"share":"https://www.laohu8.com/m/news/1154584198?lang=zh_cn&edition=full","pubTime":"2026-06-23 20:03","pubTimestamp":1782216238,"startTime":"0","endTime":"0","summary":"Calidi Biotherapeutics宣布，任命在生物技术领域拥有丰富经验的前基因泰克/罗氏及Celgene公司高管Corsee Sanders博士加入其董事会。此项人事任命旨在强化公司的战略指导与治理能力。","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":"executive","news_rank":0,"length":0,"strategy_id":0,"source":null,"symbols":["LEGN","BK4585","BK4139","BK4588","RARE","CLDI","BK4505"],"isVideo":false,"video":null,"gpt_icon":0},{"id":"1106153135","title":"Ultragenyx 根据纳斯达克上市规则授予员工入职激励股权","url":"https://stock-news.laohu8.com/highlight/detail?id=1106153135","media":"投资观察","labels":["shareholding"],"top":-1,"itemType":null,"share":"https://www.laohu8.com/m/news/1106153135?lang=zh_cn&edition=full","pubTime":"2026-06-20 04:30","pubTimestamp":1781901039,"startTime":"0","endTime":"0","summary":"专注于研发和商业化罕见及超罕见疾病创新疗法的生物制药公司 Ultragenyx Pharmaceutical Inc. 今日宣布，根据纳斯达克上市规则 5635，公司已向 15 名新入职的非高管人员授予了 44,409 份公司普通股限制性股票单位。该奖项由公司董事会薪酬委员会批准，依据 Ultragenyx 员工入职激励计划授予，授予日期为 2026 年 6 月 16 日，旨在作为吸引新员工加入公司的重要激励措施。Ultragenyx 的战略立足于高效、经济的药物开发，目标是以最快的速度向患者提供安全有效的疗法。","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":"1","news_top_title":null,"news_tag":"shareholding","news_rank":0,"length":0,"strategy_id":0,"source":null,"symbols":["RARE","BK4139","NQmain"],"isVideo":false,"video":null,"gpt_icon":0},{"id":"1139455884","title":"Ultragenyx宣布美国FDA接受UX111 AAV基因疗法BLA重新提交，用于治疗A型圣菲利波综合征（MPS IIIA）","url":"https://stock-news.laohu8.com/highlight/detail?id=1139455884","media":"美股速递","labels":["productRelease"],"top":-1,"itemType":null,"share":"https://www.laohu8.com/m/news/1139455884?lang=zh_cn&edition=full","pubTime":"2026-04-02 20:32","pubTimestamp":1775133132,"startTime":"0","endTime":"0","summary":"Ultragenyx Pharmaceutical（纳斯达克代码：RARE）近日宣布，美国食品药品监督管理局（FDA）已正式受理其针对UX111 AAV基因疗法的生物制品许可申请（BLA）重新提交。该疗法旨在治疗A型圣菲利波综合征（又称黏多糖贮积症IIIA型，MPS IIIA）。\n此次BLA重新提交标志着公司在推进该罕见病治疗领域的重要进展。UX111作为一种创新基因疗法，通过腺相关病毒载体递送功能性基因，有望为MPS IIIA患者提供新的治疗选择。\nFDA的受理决定将启动相关审评流程，后续进展备受市场关注。","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":["BK4139","RARE"],"isVideo":false,"video":null,"gpt_icon":0},{"id":"1160853916","title":"Ultragenyx宣布FDA批准UX016研究性新药申请，用于治疗GNE肌病","url":"https://stock-news.laohu8.com/highlight/detail?id=1160853916","media":"美股速递","labels":["productRelease"],"top":-1,"itemType":null,"share":"https://www.laohu8.com/m/news/1160853916?lang=zh_cn&edition=full","pubTime":"2026-03-30 20:32","pubTimestamp":1774873951,"startTime":"0","endTime":"0","summary":"Ultragenyx 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Pharmaceutical（纳斯达克代码：RARE）宣布，其创新疗法DTx301在治疗周期第36周时展现出显著疗效——患者24小时血浆氨水平较安慰剂组平均降低18%。该数据来自针对尿素循环障碍患者的二期临床试验，证实了DTx301在持续控制血氨方面的临床价值。","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":["RARE","BK4139"],"isVideo":false,"video":null,"gpt_icon":0},{"id":"1172387552","title":"Ultragenyx Pharmaceutical Inc：DTX301组高氨血症危象减少且无死亡病例，优于安慰剂","url":"https://stock-news.laohu8.com/highlight/detail?id=1172387552","media":"美股速递","labels":["dataReport"],"top":-1,"itemType":null,"share":"https://www.laohu8.com/m/news/1172387552?lang=zh_cn&edition=full","pubTime":"2026-03-12 20:33","pubTimestamp":1773318804,"startTime":"0","endTime":"0","summary":"Ultragenyx Pharmaceutical Inc公布的研究数据显示，与安慰剂组相比，其试验性疗法DTX301在治疗期间显著减少了高氨血症危象的发生次数，且该组未出现任何死亡病例。","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":"1102014175","title":"Ultragenyx Pharmaceutical Inc：治疗负担减轻次要终点数据预计2027年上半年公布","url":"https://stock-news.laohu8.com/highlight/detail?id=1102014175","media":"美股速递","labels":[],"top":-1,"itemType":null,"share":"https://www.laohu8.com/m/news/1102014175?lang=zh_cn&edition=full","pubTime":"2026-03-12 20:33","pubTimestamp":1773318803,"startTime":"0","endTime":"0","summary":"Ultragenyx Pharmaceutical Inc 近日透露，其关于减轻治疗负担的次要终点数据，预计将在2027年上半年公布。","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":"","news_rank":0,"length":0,"strategy_id":0,"source":null,"symbols":["BK4139","RARE"],"isVideo":false,"video":null,"gpt_icon":0},{"id":"1187091525","title":"Ultragenyx公布DTX301 AAV8基因疗法治疗鸟氨酸氨甲酰基转移酶缺乏症三期研究36周积极数据","url":"https://stock-news.laohu8.com/highlight/detail?id=1187091525","media":"美股速递","labels":["dataReport"],"top":-1,"itemType":null,"share":"https://www.laohu8.com/m/news/1187091525?lang=zh_cn&edition=full","pubTime":"2026-03-12 20:32","pubTimestamp":1773318743,"startTime":"0","endTime":"0","summary":"Ultragenyx Pharmaceutical Inc（简称Ultragenyx）近日宣布，其针对鸟氨酸氨甲酰基转移酶（OTC）缺乏症研发的DTX301 AAV8基因疗法，在三期临床研究中取得了36周的积极数据。这一进展标志着该基因疗法在长期疗效与安全性方面展现出令人鼓舞的结果。","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":"1144173737","title":"Ultragenyx宣布美国FDA受理DTX401 AAV基因疗法生物制剂许可申请并授予优先审评资格 用于治疗Ia型糖原贮积症","url":"https://stock-news.laohu8.com/highlight/detail?id=1144173737","media":"美股速递","labels":["productRelease"],"top":-1,"itemType":null,"share":"https://www.laohu8.com/m/news/1144173737?lang=zh_cn&edition=full","pubTime":"2026-02-23 21:31","pubTimestamp":1771853480,"startTime":"0","endTime":"0","summary":"Ultragenyx Pharmaceutical Inc宣布，其针对Ia型糖原贮积症（GSDIa）的AAV基因疗法DTX401的生物制剂许可申请（BLA），已获得美国食品药品监督管理局（FDA）的受理并被授予优先审评资格。\n此项决定标志着DTX401在迈向商业化应用的道路上取得了关键性监管进展。优先审评资格的授予，通常意味着FDA认为该疗法有潜力在治疗、诊断或预防严重疾病的安全性或有效性方面提供显著改进。\n这一里程碑将为患有此种罕见遗传性代谢疾病的患者带来新的治疗希望。","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":["BK4139","RARE"],"isVideo":false,"video":null,"gpt_icon":0},{"id":"1160301768","title":"异动解读 | 财务展望引发增长担忧，Ultragenyx Pharmaceutical盘后大跌5.32%","url":"https://stock-news.laohu8.com/highlight/detail?id=1160301768","media":"异动解读","labels":["movement"],"top":-1,"itemType":null,"share":"https://www.laohu8.com/m/news/1160301768?lang=zh_cn&edition=full","pubTime":"2026-02-13 07:01","pubTimestamp":1770937261,"startTime":"0","endTime":"0","summary":"生物制药公司Ultragenyx Pharmaceutical今日盘后股价大幅下跌5.32%，引起了市场的广泛关注。然而，在生物制药行业，研发投入通常被视为未来增长的关键驱动力，因此，持平或微降的开支展望可能引发了投资者对公司未来创新能力和增长潜力的担忧，从而导致了股价的下跌。Ultragenyx Pharmaceutical的这一财务展望，可能被部分投资者解读为公司在平衡短期财务表现与长期增长投入之间做出了偏保守的选择，进而影响了市场情绪。","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":"-1","news_top_title":null,"news_tag":"movement","news_rank":0,"length":0,"strategy_id":0,"source":"ai_movement_cn","symbols":["RARE"],"isVideo":false,"video":null,"gpt_icon":0},{"id":"1103742029","title":"Ultragenyx Pharmaceutical Inc预计2026年现有产品总收入将达7.3亿至7.6亿美元","url":"https://stock-news.laohu8.com/highlight/detail?id=1103742029","media":"美股速递","labels":["dataReport"],"top":-1,"itemType":null,"share":"https://www.laohu8.com/m/news/1103742029?lang=zh_cn&edition=full","pubTime":"2026-02-13 05:24","pubTimestamp":1770931452,"startTime":"0","endTime":"0","summary":"生物制药公司Ultragenyx Pharmaceutical Inc近日发布业绩展望，预计到2026年，其现有产品线带来的总收入将达到7.3亿至7.6亿美元区间。这一预测凸显了公司核心产品的市场增长潜力。\n该营收预期反映了公司对现有疗法商业化进程的充分信心。通过持续拓展适应症范围与优化市场渗透策略，Ultragenyx正稳步推进其罕见病治疗产品的全球布局。","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":"1142157088","title":"Ultragenyx Pharmaceutical预计2026年研发与行政开支总和将较2025年持平或微降","url":"https://stock-news.laohu8.com/highlight/detail?id=1142157088","media":"美股速递","labels":[],"top":-1,"itemType":null,"share":"https://www.laohu8.com/m/news/1142157088?lang=zh_cn&edition=full","pubTime":"2026-02-13 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AAV基因疗法治疗Ia型糖原贮积症的生物制品许可申请。这一里程碑标志着该创新疗法在监管审批道路上迈出关键一步，为罕见病患者带来新的治疗希望。DTX401作为针对GSDIa的基因治疗产品，采用腺相关病毒载体技术，旨在通过单次给药实现长期疗效。若最终获批，该疗法将填补GSDIa领域精准治疗的空白，重塑罕见病治疗格局。","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":"2595715068","title":"华尔街顶级分析师最新评级：DigitalBridge遭下调评级","url":"https://stock-news.laohu8.com/highlight/detail?id=2595715068","media":"环球市场播报","labels":[],"top":-1,"itemType":null,"share":"https://www.laohu8.com/m/news/2595715068?lang=zh_cn&edition=full","pubTime":"2025-12-31 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