美股詳情

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4.82

+0.02000.42%

成交量：21.48萬

成交額：103.42萬

市值：2.32億

市盈率：30.79

高：4.89

開：4.89

低：4.73

收：4.80

資料載入中...

總覽公司新聞資訊公告

國家外匯管理局：3月我國國際收支貨物和服務貿易進出口規模42704億元，同比增長6%

NEXUS：本季度上線 Testnet III，Q3 上線 Mainnet I

NEXUS：本季度上線Testnet III，Q3上線Mainnet I

米哈遊璃月科技公司增資至4億元

一品紅：AR882全球III期臨牀進展順利，有望搶佔痛風治療市場

康方生物(09926)依沃西聯合化療對比替雷利珠單抗聯合化療一線治療SQ -NSCLC的AK112 -306/HARMONI -6 III期臨牀達到PFS顯著陽性結果

核反應堆開發商Terra Innovatum將通過SPAC上市

【新版國家地理信息公共服務平臺正式上線】從自然資源部瞭解到，新版國家地理信息公共服務平臺“天地圖”正式上線，彙集了規劃、林草、地調、海洋等地理信息數據，增設了18個專題板塊，為社會提供更加豐富的基礎地理信息服務。自然資源部表示，隨着我國對測繪地理信息數據的需求日益旺盛，相關公共服務能力持續提升。目前，“天地圖”註冊開發用戶超過124萬個，支撐各類應用超過100萬個，地圖服務日均訪問量超過10億次。下一步，還將為水利、農業、氣象、交通、應急等行業領域提供更加豐富的專業地理信息服務支撐。

信息服務盤中異動股價大跌5.11%

工業和信息化部：取消互聯網接入服務、信息服務等業務的外商投資股比限制

【百奧泰：注射用BAT7111獲藥物臨牀試驗批准】百奧泰公告，公司於近日收到國家藥監局覈准簽發的《藥物臨牀試驗批准通知書》，公司在研藥品注射用BAT7111用於晚期實體瘤的臨牀試驗申請獲得批准。根據《Clinical Development Success Rates2011-2020》公佈的數據，通常情況下對於抗腫瘤藥物，一般I/II期臨牀研究階段持續約2年時間，I期完成進入II期的比率約48.8%，II期完成進入III期的比率約24.6%。考慮到臨牀研究週期長、投入大，過程中不可預測因素較多，臨牀試驗、審評和審批的結果以及時間都具有一定的不確定性。

十年來首個，第一三共/阿斯利康“德曲妥珠單抗”III期中期分析取得積極結果

天音控股在內蒙古成立信息服務公司含5G相關業務

天音控股在內蒙古成立信息服務公司含5G相關業務

天音控股在內蒙古成立信息服務公司，含5G相關業務

【一品紅：1類創新藥AR882全球III期臨牀已入組上千人】一品紅官微消息，公司在研全球1類創新藥AR882全球III期臨牀快速進展，目前全球已入組上千人。AR882是去年美國食品藥品監督管理局授予給中國企業快速通道資格中唯一非腫瘤類藥物，用於痛風石研究，有望填補痛風石治療領域口服藥物的全球空白。

第 12 項！默沙東啓動科倫博泰 TROP2 ADC III 期臨牀試驗

Insight数据库

商務部：擴大增值電信業務對外開放，加大軟件和信息服務業對外開放力度

禮來(LLY.US)口服小分子GLP-1R激動劑III期研究成功

兆科眼科-B(06622)：環孢素A眼凝膠新一輪第III期臨牀試驗入組首名患者

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Rates2011-2020》公佈的數據，通常情況下對於抗腫瘤藥物，一般I/II期臨牀研究階段持續約2年時間，I期完成進入II期的比率約48.8%，II期完成進入III期的比率約24.6%。考慮到臨牀研究週期長、投入大，過程中不可預測因素較多，臨牀試驗、審評和審批的結果以及時間都具有一定的不確定性。","url":"https://stock-news.laohu8.com/highlight/detail?id=2529288268","media":"金融界","labels":["productRelease"],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2529288268?lang=zh_tw&edition=fundamental","pubTime":"2025-04-21 15:42","pubTimestamp":1745221338,"startTime":"0","endTime":"0","summary":"百奥泰公告，公司于近日收到国家药监局核准签发的《药物临床试验批准通知书》，公司在研药品注射用BAT7111用于晚期实体瘤的临床试验申请获得批准。根据《Clinical Development Success 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期臨牀試驗","url":"https://stock-news.laohu8.com/highlight/detail?id=2528595000","media":"Insight数据库","labels":[],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2528595000?lang=zh_tw&edition=fundamental","pubTime":"2025-04-18 17:23","pubTimestamp":1744968229,"startTime":"0","endTime":"0","summary":"4 月 18 日，中国药物临床试验登记与信息公示平台显示，默沙东登记了一项比较 Sac-TMT联合/不联合帕博利珠单抗与 TPC一线治疗不可切除/转移性三阴性乳腺癌的 III 期研究。Insight 数据库显示，这是默沙东针对该药启动的第 12 项全球多中心临床试验。该药首次于 2024 年 11 月获 NMPA 批准上市，用于三阴性乳腺癌的二线治疗。2022 年 5 月，科伦博泰与默沙东签署合作协议，授予后者在大中华区以外的所有地区开发、使用、制造及商业化Sac-TMT 的独家权利。","market":"us","thumbnail":null,"type":0,"news_type":0,"thumbnails":[],"rights":{"source":"tencent","url":"http://gu.qq.com/resources/shy/news/detail-v2/index.html#/?id=nesSN20250418172807a6bf22a3&s=b","rn_cache_url":null,"customStyle":"body{padding-top:10px;}#news_title{font-weight:bold;#titleStyle#;}#news_description span{font-size:12px;#descriptionStyle#;}.footer-note{#statement#}","selectors":".mod-LoadTzbdNews, 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