美股詳情

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三倍做多標普生物-Direxion

261.30

-4.7000-1.77%

盤後：261.300.00000.00%19:58 EDT

成交量：22.74萬

成交額：6,097.03萬

市值：4.90億

市盈率：- -

高：278.96

開：273.29

低：261.30

收：266.00

52周最高：341.93

52周最低：74.95

股本：187.45萬

流通股本：187.45萬

量比：0.94

換手率：12.13%

股息：1.00

股息率：0.38%

淨資產收益率：--

總資產收益率：--

市淨率：--

市盈率(LYR):- -

資料載入中...

總覽公司新聞公告

醫療保健板塊動態：市場快評

上海國投先導聯合領投，NewPro完成數千萬元PreA輪融資並獲得乳鐵蛋白FDA Self-GRAS認證

FDA授予Xellsmart帕金森病現貨型細胞療法快速通道資格

环球市场播报

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海西新藥(02637)：HX9428治療新生血管性年齡相關性黃斑變性獲美國FDA IND批准啓動II期臨床試驗同時在中國啓動第二項採用陽性對照的II期臨床試驗

美國 FDA 授予再鼎醫藥靶向 DLL3 抗體藥物偶聯物 Zocilurtatug Pelitecan（Zoci）孤兒藥資格認定，用於治療神經內分泌癌（NEC）

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【今日主題前瞻】AI醫療健康解決方案市場規模2030年或突破1000億元

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諾華宣佈Pluvicto獲FDA批准用於PSMA陽性轉移性激素敏感性前列腺癌，有望推動轉移性前列腺癌治療新標準。

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泰德醫藥(03880.HK)成功完成HEPCLUDEX®原料藥之美國FDA上市許可前檢查(PLI)

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21:07","pubTimestamp":1785848846,"startTime":"0","endTime":"0","summary":"XellSmart专有的现货型iPSC衍生细胞疗法XS411获得美国FDA快速通道资格，标志着其全球临床开发的重要里程碑。　　2026年7月28日，XellSmart宣布，其自主研发的针对帕金森病的同种异体、现货型、可注射iPSC衍生细胞疗法候选产品XS411，已正式获得美国食品药品监督管理局授予的快速通道资格。这一监管认定彰显了美国卫生监管机构对XS411临床价值及其解决帕金森病治疗中重大未满足临床需求潜力的认可，是其全球临床开发和未来市场准入的关键里程碑。","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":"https://finance.sina.com.cn/stock/usstock/c/2026-08-04/doc-inimeknz5555117.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_us","symbols":["SYNB","CNCR","BK4585","WDNA","BK4588","LABU"],"isVideo":false,"video":null,"gpt_icon":0},{"id":"2656597285","title":"艾伯維（ABBV）保妥適新適應症獲FDA受理 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IND批准啓動II期臨床試驗 同時在中國啓動第二項採用陽性對照的II期臨床試驗","url":"https://stock-news.laohu8.com/highlight/detail?id=2656460539","media":"智通财经","labels":["productRelease"],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2656460539?lang=zh_tw&edition=fundamental","pubTime":"2026-08-04 17:15","pubTimestamp":1785834956,"startTime":"0","endTime":"0","summary":"此次获批的IND涵盖一项II期临床试验方案，旨在评估HX9428不同口服剂量在美国 nAMD患者中的有效性及安全性。该研究为集团在HX9428既往I 期及II期剂量扩展研究的基础上，进一步启动的一项随机、阳性对照的II期临床研究。本次美国FDAII期临床试验获批、中国标准疗法对照II期临床试验启动，标志着 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Pelitecan（Zoci）孤兒藥資格認定，用於治療神經內分泌癌（NEC）","url":"https://stock-news.laohu8.com/highlight/detail?id=2656210587","media":"美通社","labels":["policyRegulatory"],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2656210587?lang=zh_tw&edition=fundamental","pubTime":"2026-08-04 13:48","pubTimestamp":1785822480,"startTime":"0","endTime":"0","summary":"神经内分泌癌是一类高侵袭性恶性肿瘤，预后差且治疗选择有限，存在重大未被满足的临床需求 继欧洲药品管理局授予 zoci 孤儿药资格认定用于治疗肺神经内分泌癌之后，此次获美国 FDA 授予ODD，进一步印证了 zoci 在各类神经内分泌癌领域具有同类首创潜力  中国上海和美国马萨诸塞州剑桥2026年8月4日 /美通社/ -- 再鼎医药有限公司今日宣布，美国食品药品监督管理局已授予 zocilurtatug pelitecan孤儿药资格认定，用于治疗神经内分泌癌。","market":"us","thumbnail":null,"type":0,"news_type":0,"thumbnails":[],"rights":{"source":"prnasia","url":"http://wwwold.prnasia.com/story/archive/5018636_ZH18636_1","rn_cache_url":null,"directOrigin":true},"property":[],"language":"zh","translate_title":"","themeId":null,"theme_name":"","theme_type":"","isJumpTheme":false,"source_url":"http://wwwold.prnasia.com/story/archive/5018636_ZH18636_1","is_publish_highlight":false,"source_rank":0,"column":"","sentiment":"1","news_top_title":null,"news_tag":"policyRegulatory","news_rank":0,"length":0,"strategy_id":0,"source":"prnasia","symbols":["BK4526","BK1588","BK4139","BK4548","LU2488822045.USD","BK1574","BK4531","ZLAB","BK1161","BK4588","BK4585","09688","LABU"],"isVideo":false,"video":null,"gpt_icon":0},{"id":"1198971052","title":"醫療健康板塊快訊：市場動態一覽","url":"https://stock-news.laohu8.com/highlight/detail?id=1198971052","media":"投资观察","labels":[],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/1198971052?lang=zh_tw&edition=fundamental","pubTime":"2026-08-04 04:56","pubTimestamp":1785790601,"startTime":"0","endTime":"0","summary":"分析师指出，尽管投资者此前主要担忧仿制药会蚕食其畅销抗癌药Somatuline的销售额，但瑞典Camurus公司的实验性药物CAM2029才是更长期的威胁。一项针对CAM2029治疗神经内分泌肿瘤的晚期研究结果将于2026年底或2027年初公布，分析人士认为，其结果很可能会优于Somatuline。考虑到Somatuline贡献了益普生约30%的销售额且利润极高，这无疑会给公司盈利带来巨大压力。Jefferies因此将益普生的评级从“持有”下调至“跑输大盘”。受此影响，其股价下跌8.2%，报153.50欧元。","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":"0","news_top_title":null,"news_tag":"","news_rank":0,"length":0,"strategy_id":0,"source":null,"symbols":["XLV","XBI","BK4585","BK4581","LABU","BK4588"],"isVideo":false,"video":null,"gpt_icon":0},{"id":"1176302759","title":"醫療保健板塊綜述：市場快訊","url":"https://stock-news.laohu8.com/highlight/detail?id=1176302759","media":"投资观察","labels":[],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/1176302759?lang=zh_tw&edition=fundamental","pubTime":"2026-08-04 00:25","pubTimestamp":1785774322,"startTime":"0","endTime":"0","summary":"1007 ET - 杰富瑞分析师表示，益普生旗下最畅销的药物可能很快将面临来自瑞典卡穆鲁斯的竞争。投资者此前主要关注的是仿制药进入市场、侵蚀其旗舰抗癌药索马杜林销售的风险，但杰富瑞认为，更大的长期风险实则来自卡穆鲁斯的实验性药物CAM2029。杰富瑞随后将益普生的评级从“持有”下调至“跑输大盘”。益普生股价下跌8.2%，报153.50欧元。","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":"0","news_top_title":null,"news_tag":"","news_rank":0,"length":0,"strategy_id":0,"source":null,"symbols":["LABU","XBI","BK4585","BK4581","XLV","BK4588"],"isVideo":false,"video":null,"gpt_icon":0},{"id":"2656747793","title":"美國人已經為多肽而瘋狂，這是你可能關心的5個問題","url":"https://stock-news.laohu8.com/highlight/detail?id=2656747793","media":"虎嗅APP","labels":[],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2656747793?lang=zh_tw&edition=fundamental","pubTime":"2026-08-03 17:47","pubTimestamp":1785750420,"startTime":"0","endTime":"0","summary":"但此次FDA咨询委员会投票的多肽，都是没有经过批准的产品，人们通过黑市或者长寿诊所私下购买，用来抗衰、恢复体力、改善睡眠、提升脑力等。但咨询委员会这一小步，是美国人为多肽疯狂的一大步。FDA官网显示，这届投票委员会小组共12人，至少8人是 2026年新获任命的，其中至少7名新任委员，与多肽产业有关联，或本身就是多肽政策的推动者。鉴于美国FDA在全球卫生体系中的影响力，此次对多肽开绿灯，后果也将波及全世界。","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://mp.weixin.qq.com/s?__biz=MTQzMjE1NjQwMQ==&mid=2656191260&idx=3&sn=9447f651dbbeee189256ddf2f27cdd28&chksm=676248f6d0d526ebc910b879d3a514abec3d7e6450ac1abc85b3232a4b3f7c9744fda2a40f96&scene=0#rd","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":"weixin_highlight","symbols":["HHS","BK4585","BK4009","LABU","BK4588"],"isVideo":false,"video":null,"gpt_icon":0},{"id":"1123567512","title":"醫療保健動態：市場快訊","url":"https://stock-news.laohu8.com/highlight/detail?id=1123567512","media":"投资观察","labels":[],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/1123567512?lang=zh_tw&edition=fundamental","pubTime":"2026-08-03 16:27","pubTimestamp":1785745649,"startTime":"0","endTime":"0","summary":"**0811 GMT** - 杰富瑞分析师指出，阿斯利康与百时美施贵宝之间潜在的合并交易，可能因双方产品组合重叠而面临反垄断障碍，并附带政治层面的考量。《金融时报》报道称两家公司曾进行合并谈判，阿斯利康对此不予置评，而百时美施贵宝未回应置评请求。此外，他们补充道，阿斯利康还需妥善处理交易的政治因素，以减少摩擦。欧洲早盘交易中，阿斯利康股价下跌6.2%。百时美施贵宝股价在美股盘前交易中上涨4.5%。","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":["XBI","BK4588","BK4581","LABU","BK4585","XLV"],"isVideo":false,"video":null,"gpt_icon":0},{"id":"2656329169","title":"天智航「蛇吞象式」收購拖累報表？三大疑問待解 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