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4.82

+0.02000.42%

盘后：4.71-0.1100-2.28%19:52 EDT

成交量：21.48万

成交额：103.42万

市值：2.33亿

市盈率：30.79

高：4.89

开：4.89

低：4.73

收：4.80

数据加载中...

总览公司新闻资讯公告

一品红：AR882全球III期临床进展顺利，有望抢占痛风治疗市场

康方生物(09926)依沃西联合化疗对比替雷利珠单抗联合化疗一线治疗SQ -NSCLC的AK112 -306/HARMONI -6 III期临床达到PFS显著阳性结果

核反应堆开发商Terra Innovatum将通过SPAC上市

【新版国家地理信息公共服务平台正式上线】从自然资源部了解到，新版国家地理信息公共服务平台“天地图”正式上线，汇集了规划、林草、地调、海洋等地理信息数据，增设了18个专题板块，为社会提供更加丰富的基础地理信息服务。自然资源部表示，随着我国对测绘地理信息数据的需求日益旺盛，相关公共服务能力持续提升。目前，“天地图”注册开发用户超过124万个，支撑各类应用超过100万个，地图服务日均访问量超过10亿次。下一步，还将为水利、农业、气象、交通、应急等行业领域提供更加丰富的专业地理信息服务支撑。

信息服务盘中异动股价大跌5.11%

工业和信息化部：取消互联网接入服务、信息服务等业务的外商投资股比限制

【百奥泰：注射用BAT7111获药物临床试验批准】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 Rates2011-2020》公布的数据，通常情况下对于抗肿瘤药物，一般I/II期临床研究阶段持续约2年时间，I期完成进入II期的比率约48.8%，II期完成进入III期的比率约24.6%。考虑到临床研究周期长、投入大，过程中不可预测因素较多，临床试验、审评和审批的结果以及时间都具有一定的不确定性。

十年来首个，第一三共/阿斯利康“德曲妥珠单抗”III期中期分析取得积极结果

天音控股在内蒙古成立信息服务公司含5G相关业务

天音控股在内蒙古成立信息服务公司含5G相关业务

天音控股在内蒙古成立信息服务公司，含5G相关业务

【一品红：1类创新药AR882全球III期临床已入组上千人】一品红官微消息，公司在研全球1类创新药AR882全球III期临床快速进展，目前全球已入组上千人。AR882是去年美国食品药品监督管理局授予给中国企业快速通道资格中唯一非肿瘤类药物，用于痛风石研究，有望填补痛风石治疗领域口服药物的全球空白。

第 12 项！默沙东启动科伦博泰 TROP2 ADC III 期临床试验

Insight数据库

商务部：扩大增值电信业务对外开放，加大软件和信息服务业对外开放力度

礼来(LLY.US)口服小分子GLP-1R激动剂III期研究成功

兆科眼科-B(06622)：环孢素A眼凝胶新一轮第III期临床试验入组首名患者

布雷顿森林体系 III ：Zoltan数年前的预言，正在2025年骤然展开

【百利天恒：BL-B01D1（EGFR×HER3 双抗 ADC）联合用药治疗多种晚期实体瘤获 4 个 II 期药物临床试验批准通知书】金融界4月15日消息，百利天恒近日收到国家药品监督管理局正式批准签发的 4 个《药物临床试验批准通知书》，公司自主研发的创新生物药注射用 BL-B01D1（EGFR×HER3 双抗 ADC）的 4 个联合用药的 II 期临床试验获得批准。注射用 BL-B01D1 临床试验符合药品注册要求，同意开展联合仑伐替尼用于晚期肝癌、联合阿昔替尼±帕博利珠单抗用于晚期肾癌、联合贝伐珠单抗±化疗用于晚期结直肠癌、联合帕博利珠单抗±化疗用于晚期胆道恶性肿瘤的临床试验。BL-B01D1 是全球首创且唯一进入 III 期临床阶段的 EGFR×HER3 双抗 ADC，除本次新批准的 4 项临床试验外，正在中国和美国进行 30 余项针对十余种肿瘤类型的临床试验。药品需完成相关临床试验并通过审评、审批后方可上市销售，医药产品具有诸多特点，从研究到投产环节多，易受不确定性因素影响。

玉龙股份：本次终止上市事项开设现金选择权信息服务

万泰生物：九价HPV疫苗启动男性III期临床试验并完成首例受试者入组

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期临床试验","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_cn&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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