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Ultragenyx Pharmaceutical Inc

23.39

-0.3200-1.35%

盤後：23.390.00000.00%19:17 EDT

成交量：113.06萬

成交額：2,651.75萬

市值：23.00億

市盈率：-3.83

高：24.12

開：23.68

低：23.26

收：23.71

52周最高：42.37

52周最低：18.29

股本：9,831.72萬

流通股本：9,449.35萬

量比：0.71

換手率：1.20%

股息：- -

股息率：- -

每股收益(TTM):-6.1099

每股收益(LYR):-5.8316

淨資產收益率：-608.47%

總資產收益率：-25.45%

市淨率：-9.74

市盈率(LYR):-4.01

資料載入中...

總覽公司新聞資訊公告

BUZZ-美國食品和藥物管理局接受罕見病療法上市申請後，Ultragenyx 股價上漲

Ultragenyx宣佈美國FDA接受UX111 AAV基因療法BLA重新提交，用於治療A型聖菲利波綜合徵（MPS IIIA）

Ultragenyx Pharmaceutical Inc - 若獲批，UX111將在美國Andelyn Biosciences及Ultragenyx工廠生產

BUZZ-FDA批准罕見肌病藥物人體試驗後，Ultragenyx股價上漲

Ultragenyx宣佈FDA批准UX016研究性新藥申請，用於治療GNE肌病

在後期研究中，Ultragenyx 公司的基因療法有助於控制氨水平

Ultragenyx製藥DTx301第36周24小時血漿氨水平較安慰劑降低18%

Ultragenyx Pharmaceutical Inc：DTX301組高氨血癥危象減少且無死亡病例，優於安慰劑

Ultragenyx Pharmaceutical Inc：治療負擔減輕次要終點數據預計2027年上半年公布

Ultragenyx公布DTX301 AAV8基因療法治療鳥氨酸氨甲酰基轉移酶缺乏症三期研究36周積極數據

Ultragenyx宣佈美國FDA受理DTX401 AAV基因療法生物製劑許可申請並授予優先審評資格用於治療Ia型糖原貯積症

異動解讀 | 財務展望引發增長擔憂，Ultragenyx Pharmaceutical盤後大跌5.32%

Ultragenyx Pharmaceutical Inc預計2026年現有產品總收入將達7.3億至7.6億美元

Ultragenyx Pharmaceutical預計2026年研發與行政開支總和將較2025年持平或微降

Ultragenyx Pharmaceutical預計2027年研發支出將較2025年水平下降38%，約2.8億美元

BUZZ-Ultragenyx 股價上漲，基因療法對罕見兒童腦病展現長期療效

Ultragenyx Pharmaceutical Inc 研究成果：生物標誌物顯著改善並帶來功能性獲益

Ultragenyx公布UX111基因療法長期積極數據：顯著持續降低腦脊液硫酸乙酰肝素水平，並在桑菲利波綜合徵（MPS IIIA）患兒多發育領域實現臨床功能持續改善

Ultragenyx重新向美國FDA提交UX111基因療法治療A型Sanfilippo綜合徵的生物製品許可申請

數據：ROSE 24 小時跌超 11%，RARE 升逾 14%

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旗下基因疗法UX111的生产将落地美国，计划在Andelyn Biosciences公司与Ultragenyx自有设施同步展开。这一双线布局旨在强化供应链韧性，为未来商业化推进提供产能保障。","market":"us","thumbnail":"","type":0,"news_type":0,"thumbnails":[],"rights":null,"property":[],"language":"zh","translate_title":"","themeId":"","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":"2623100563","title":"BUZZ-FDA批准罕見肌病藥物人體試驗後，Ultragenyx股價上漲","url":"https://stock-news.laohu8.com/highlight/detail?id=2623100563","media":"路透中文","labels":["productRelease"],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2623100563?lang=zh_tw&edition=fundamental","pubTime":"2026-03-30 20:47","pubTimestamp":1774874833,"startTime":"0","endTime":"0","summary":"BUZZ-FDA批准罕见肌病药物人体试验后，Ultragenyx股价上涨3月30日 - ** 制药公司Ultragenyx Pharmaceutical RARE.O股价盘前上涨2%至19.76美元** 该公司称美国FDA批准了其开始对UX016进行人体试验的申请，以治疗GNE肌病，这是一种罕见的遗传性肌肉疾病，会导致肌无力和残疾恶化** 公司表示，目前还没有获准治疗这种疾病的药物，在可进入的商业市场中，约有 10,000 人患有这种疾病。对于因为使用自动化翻译功能而造成的任何损害或损失，路透不承担任何责任。","market":"hk","thumbnail":null,"type":0,"news_type":0,"thumbnails":[],"rights":null,"property":[],"language":"zh","translate_title":"","themeId":"37684715aaf54a73b9fe52ee56a263cc","theme_name":"","theme_type":"","isJumpTheme":false,"source_url":"https://api.refinitiv.com/data/news/v1/stories/urn:newsml:reuters.com:20260330:nL4T40I16U: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":["BK4139","RARE"],"isVideo":false,"video":null,"gpt_icon":0},{"id":"1160853916","title":"Ultragenyx宣佈FDA批准UX016研究性新藥申請，用於治療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://ttm.financial/m/news/1160853916?lang=zh_tw&edition=fundamental","pubTime":"2026-03-30 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RARE.O公司周四称，其实验性基因疗法在一项后期试验中帮助患者更好地控制了与一种罕见遗传性疾病相关的氨水平。(为便利非英文母语者，路透将其报导自动化翻译为数种其他语言。由于自动化翻译可能有误，或未能包含所需语境，路透不保证自动化翻译文本的准确性，仅是为了便利读者而提供自动化翻译。对于因为使用自动化翻译功能而造成的任何损害或损失，路透不承担任何责任。)","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:20260312:nL4T4001A9:1","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":["RARE","BK4139"],"isVideo":false,"video":null,"gpt_icon":0},{"id":"1176626417","title":"Ultragenyx製藥DTx301第36周24小時血漿氨水平較安慰劑降低18%","url":"https://stock-news.laohu8.com/highlight/detail?id=1176626417","media":"美股速递","labels":["dataReport"],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/1176626417?lang=zh_tw&edition=fundamental","pubTime":"2026-03-12 20:33","pubTimestamp":1773318808,"startTime":"0","endTime":"0","summary":"Ultragenyx 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":"","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組高氨血癥危象減少且無死亡病例，優於安慰劑","url":"https://stock-news.laohu8.com/highlight/detail?id=1172387552","media":"美股速递","labels":["dataReport"],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/1172387552?lang=zh_tw&edition=fundamental","pubTime":"2026-03-12 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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":"","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":"1144173737","title":"Ultragenyx宣佈美國FDA受理DTX401 AAV基因療法生物製劑許可申請並授予優先審評資格 用於治療Ia型糖原貯積症","url":"https://stock-news.laohu8.com/highlight/detail?id=1144173737","media":"美股速递","labels":["productRelease"],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/1144173737?lang=zh_tw&edition=fundamental","pubTime":"2026-02-23 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Pharmaceutical盤後大跌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://ttm.financial/m/news/1160301768?lang=zh_tw&edition=fundamental","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":"sg","thumbnail":"","type":0,"news_type":0,"thumbnails":[],"rights":null,"property":[],"language":"zh","translate_title":"","themeId":"","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預計2026年現有產品總收入將達7.3億至7.6億美元","url":"https://stock-news.laohu8.com/highlight/detail?id=1103742029","media":"美股速递","labels":["dataReport"],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/1103742029?lang=zh_tw&edition=fundamental","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":"","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預計2026年研發與行政開支總和將較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://ttm.financial/m/news/1142157088?lang=zh_tw&edition=fundamental","pubTime":"2026-02-13 05:23","pubTimestamp":1770931393,"startTime":"0","endTime":"0","summary":"生物制药公司Ultragenyx Pharmaceutical（纳斯达克代码：RARE）近日披露财务展望，预计2026年度研发支出与销售、一般及行政开支的总和，将较2025年水平实现持平或出现低个位数百分比的下滑。这一预算规划反映出公司通过优化运营效率，在持续投入创新药物研发的同时加强成本管控的战略方向。","market":"us","thumbnail":"","type":0,"news_type":0,"thumbnails":[],"rights":null,"property":[],"language":"zh","translate_title":"","themeId":"","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":["RARE","BK4139"],"isVideo":false,"video":null,"gpt_icon":0},{"id":"1180365196","title":"Ultragenyx Pharmaceutical預計2027年研發支出將較2025年水平下降38%，約2.8億美元","url":"https://stock-news.laohu8.com/highlight/detail?id=1180365196","media":"美股速递","labels":["dataReport"],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/1180365196?lang=zh_tw&edition=fundamental","pubTime":"2026-02-13 05:23","pubTimestamp":1770931393,"startTime":"0","endTime":"0","summary":"生物制药公司Ultragenyx Pharmaceutical Inc近日发布预测，到2027年，其研发支出预计将比2025年水平减少38%，相当于约2.8亿美元。这一调整反映了公司在完成关键临床试验后，研发管线将进入相对成熟的阶段。随着多个候选药物进入商业化准备期，公司计划将资源更多投向市场推广和产品上市工作。此次研发支出的战略性缩减，有望为公司在未来几年实现盈利增长创造有利条件。","market":"us","thumbnail":"","type":0,"news_type":0,"thumbnails":[],"rights":null,"property":[],"language":"zh","translate_title":"","themeId":"","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":"2608654874","title":"BUZZ-Ultragenyx 股價上漲，基因療法對罕見兒童腦病展現長期療效","url":"https://stock-news.laohu8.com/highlight/detail?id=2608654874","media":"路透中文","labels":["shareholding"],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2608654874?lang=zh_tw&edition=fundamental","pubTime":"2026-02-03 21:44","pubTimestamp":1770126264,"startTime":"0","endTime":"0","summary":"BUZZ-Ultragenyx 股价上涨，基因疗法对罕见儿童脑病展现长期疗效2月3日 - ** 制药商Ultragenyx RARE.O的股价在盘前交易中上涨4%至25.75美元 ** 该公司称，  其实验性基因疗法可帮助患有A型圣菲利普综合征的儿童在八年多的时间里保持关键能力。** 当人体无法分解某些物质时，A 型圣菲利普综合征就会发生，导致大脑功能严重衰退；该公司称，大多数患儿在十几岁时就会死亡。对于因为使用自动化翻译功能而造成的任何损害或损失，路透不承担任何责任。","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://api.refinitiv.com/data/news/v1/stories/urn:newsml:reuters.com:20260203:nL4S3YZ1DB:1","is_publish_highlight":false,"source_rank":0,"column":"","sentiment":"2","news_top_title":null,"news_tag":"shareholding","news_rank":0,"length":0,"strategy_id":0,"source":null,"symbols":["BK4139","RARE"],"isVideo":false,"video":null,"gpt_icon":0},{"id":"1118044429","title":"Ultragenyx Pharmaceutical Inc 研究成果：生物標誌物顯著改善並帶來功能性獲益","url":"https://stock-news.laohu8.com/highlight/detail?id=1118044429","media":"美股速递","labels":["dataReport"],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/1118044429?lang=zh_tw&edition=fundamental","pubTime":"2026-02-03 21:05","pubTimestamp":1770123913,"startTime":"0","endTime":"0","summary":"Ultragenyx Pharmaceutical Inc 公布的最新研究结果显示，其在研疗法取得了重要进展，不仅实现了生物标志物的显著改善，还为患者带来了明确的功能性获益。","market":"us","thumbnail":"","type":0,"news_type":0,"thumbnails":[],"rights":null,"property":[],"language":"zh","translate_title":"","themeId":"","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":"1111118765","title":"Ultragenyx公布UX111基因療法長期積極數據：顯著持續降低腦脊液硫酸乙酰肝素水平，並在桑菲利波綜合徵（MPS IIIA）患兒多發育領域實現臨床功能持續改善","url":"https://stock-news.laohu8.com/highlight/detail?id=1111118765","media":"美股速递","labels":["dataReport"],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/1111118765?lang=zh_tw&edition=fundamental","pubTime":"2026-02-03 21:02","pubTimestamp":1770123776,"startTime":"0","endTime":"0","summary":"Ultragenyx Pharmaceutical近日公布了其基因疗法UX111的长期随访数据，结果显示该疗法对桑菲利波综合征（MPS IIIA）患儿具有持续性的治疗效果。数据显示，接受UX111治疗的患者脑脊液中硫酸乙酰肝素（CSF-HS）水平出现显著且持久的降低，同时多个发育领域的临床功能均呈现持续有意义的改善。这些长期数据进一步验证了UX111基因疗法在改变疾病进程方面的潜力，为患有这种罕见神经退行性疾病的儿童带来了新的希望。","market":"us","thumbnail":"","type":0,"news_type":0,"thumbnails":[],"rights":null,"property":[],"language":"zh","translate_title":"","themeId":"","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":"1170251319","title":"Ultragenyx重新向美國FDA提交UX111基因療法治療A型Sanfilippo綜合徵的生物製品許可申請","url":"https://stock-news.laohu8.com/highlight/detail?id=1170251319","media":"美股速递","labels":["productRelease"],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/1170251319?lang=zh_tw&edition=fundamental","pubTime":"2026-01-30 21:32","pubTimestamp":1769779956,"startTime":"0","endTime":"0","summary":"Ultragenyx Pharmaceutical（纳斯达克代码：RARE）已正式向美国食品药品监督管理局重新递交了UX111 AAV基因疗法的生物制品许可申请。该疗法旨在治疗A型Sanfilippo综合征（又称MPS IIIA），这是一种罕见的遗传性神经退行性疾病。\n此次重新提交基于最新临床数据对申请材料进行了全面优化，标志着该基因疗法在监管审批进程中迈出关键一步。若获批，UX111将成为全球首个针对该致命性儿童罕见病的基因治疗方案。","market":"us","thumbnail":"","type":0,"news_type":0,"thumbnails":[],"rights":null,"property":[],"language":"zh","translate_title":"","themeId":"","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":"2605428607","title":"數據：ROSE 24 小時跌超 11%，RARE 升逾 14%","url":"https://stock-news.laohu8.com/highlight/detail?id=2605428607","media":"链捕手","labels":[],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2605428607?lang=zh_tw&edition=fundamental","pubTime":"2026-01-23 11:30","pubTimestamp":1769139031,"startTime":"0","endTime":"0","summary":" ChainCatcher 消息，据币安现货数据显示，市场出现大幅波动。ROSE 24 小时跌幅达 11.25%，RARE 24 小时涨幅 14.74%，并出现探底回升状态。同时，GHST、SYRUP 也出现“冲高回落”状态，24 小时跌幅分别为 7.32% 和 7.44%。其余代币如 BIGTIME、RESOLV、币安人生均出现探底回升状态，涨幅分别为 8.18%、12.39% 和 5.41%。SANTOS 则触及今日新高，涨幅 12.72%。此外，SENT 在 5 分钟内小幅下跌，跌幅为 3.04%。 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