美股詳情

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三倍做多標普生物-Direxion

250.40

-17.9900-6.70%

盤後：251.981.58+0.63%19:59 EDT

成交量：32.56萬

成交額：8,161.00萬

市值：4.94億

市盈率：- -

高：267.90

開：266.14

低：243.24

收：268.39

52周最高：341.93

52周最低：76.29

股本：197.45萬

流通股本：197.45萬

量比：1.30

換手率：16.49%

股息：1.02

股息率：0.41%

淨資產收益率：--

總資產收益率：--

市淨率：--

市盈率(LYR):- -

資料載入中...

總覽公司新聞資訊公告

聯合治療（UTHR）霧化吸入劑Tyvaso擴大適應症申請獲FDA受理

翰宇藥業(300199.SZ)：坪山分公司通過美國FDA現場檢查

翰宇藥業：坪山分公司第二次通過FDA現場檢查

醫療保健板塊動態：市場快訊匯總

美股異動 | 禮來(LLY.US)漲1.69% 阿爾茨海默病血液檢測獲FDA批准

美股異動 | 禮來(LLY.US)漲1.69% 阿爾茨海默病血液檢測獲FDA批准

FDA批准替爾泊肽用於降低T2D成人患者心血管事件風險

仙琚製藥(002332.SZ)：黃體酮陰道片獲得美國FDA註冊申請受理

仙琚製藥：100mg黃體酮陰道片ANDA獲美國FDA受理

百濟神州：PD-1抗癌藥降價加入美國公共醫療保險計劃今後上市創新藥均將執行最惠國定價

每日经济新闻

迪哲醫藥：舒沃哲新增適應症上市申請獲美國FDA受理

9月1日起，烏魯木齊靈活就業人員可參加生育保險！

新疆949交通广播

美國FDA批准胰腺癌突破性藥物獨立藥企Revolution Medicines迎里程碑

环球市场播报

中國生物製藥(01177.HK)：LM-364「NECTIN-4TMEADC」臨床試驗申請獲NMPA及FDA批准

美國FDA批准吉利德用於治療艾滋病的口服藥

莫德納獲美國FDA批准，推出2026‑2027版更新新冠疫苗。

美國食品藥品監督管理局：FDA批准首款用於治療成人皮肌炎的口服藥物。

美國 FDA：美敦力召回 2027 年 10 月 20 日前到期的 Bravo CF 相關批次產品。

加拿大皇家銀行首席執行官在電話會議上表示，市場環境總體上仍保持建設性態勢，自然資源、電力基礎設施、戰略防禦、醫療保健及人

醫療健康板塊市場動態綜述

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23:35","pubTimestamp":1788276923,"startTime":"0","endTime":"0","summary":"智通财经APP获悉，周二，礼来涨1.69%，报1176.23美元。消息面上，礼来与罗氏联合开发的Elecsys Phospho-TauPlasma血液检测已拿到美国FDA批准，用于辅助判断55岁及以上出现认知衰退症状人群，是否存在阿尔茨海默病相关脑内淀粉样蛋白病理改变。据悉，这一诊断技术直击阿尔茨海默病治疗的现实痛点。能否实现低成本、标准化、可大规模普及的筛查手段，直接决定相关药物的患者覆盖规模，也会影响新一代阿尔茨海默病药物向更早阶段人群推广的进程。","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":"http://www.zhitongcaijing.com/content/detail/1490672.html","is_publish_highlight":false,"source_rank":0,"column":"","sentiment":"0","news_top_title":null,"news_tag":"productRelease","news_rank":0,"length":0,"strategy_id":0,"source":"stock_zhitongcaijing","symbols":["BK4588","LABU","BK4585"],"isVideo":false,"video":null,"gpt_icon":0},{"id":"2664685079","title":"美股異動 | 禮來(LLY.US)漲1.69% 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