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泰格醫藥

24.450

-5.900-19.44%

成交量：706.12萬

成交額：1.84億

市值：211.48億

市盈率：49.09

高：28.400

開：28.400

低：24.100

收：30.350

資料載入中...

總覽公司新聞公告

北京推出32條支持創新醫藥高質量發展措施

港股異動 | CRO概念股跌幅居前機構稱關税對CXO及上游目前影響較為有限關注生物安全法案相關進展

泰格醫藥盤中異動股價大跌8.73%

【沛嘉醫療：完成ReachTactile機器人輔助TAVR系統首次人體臨牀試驗】沛嘉醫療公告，公司完成ReachTactile機器人輔助經導管主動脈瓣置換（TAVR）系統首次人體臨牀試驗的首例患者治療。手術由廈門大學附屬心血管病醫院的王焱教授及其團隊完成，利用ReachTactile™機器人輔助TAVR系統為一名重度主動脈瓣狹窄患者植入TaurusElite®經導管主動脈瓣膜。ReachTactile是公司內部研發的機器人輔助TAVR系統，為TAVR治療提供創新、高性價比的解決方案。

過敏性鼻炎治療研究取得新進展

業績陡降泰格醫藥困在“週期”裏

中国经营网

中國生物製藥：“TQB6411 (EGFR/c-Met雙抗ADC)”臨牀試驗申請獲CDE受理

中國生物製藥(01177)研發的抗腫瘤藥“TQB2101 (ROR1 ADC)”獲得NMPA的臨牀試驗默示許可

每日賣空追蹤 | 泰格醫藥 04月03日賣空量成交26.73萬股，賣空比例為11.86%

石四藥集團SYN045片獲三種規格一期臨牀試驗許可

【石四藥集團(02005.HK)：SYN045片已取得國藥監局新增三種不同規格(10mg、25mg及50mg)的一期臨牀試驗許可】石四藥集團(02005.HK)發佈公告，該集團的化學藥品1類新藥SYN045片已取得中國國家藥品監督管理局新增三種不同規格(10mg、25mg及50mg)的一期臨牀試驗許可，可以滿足臨牀試驗多樣化需求，針對不同年齡段患者實現劑量梯度給藥，進一步優化精準給藥方案，提升SYN045片的臨牀應用價值。

石四藥集團(02005)：SYN045片已取得國藥監局新增三種不同規格(10mg、25mg及50mg)的一期臨牀試驗許可

智通财经网

百誠醫藥(301096.SZ)創新藥BIOS-0618片獲臨牀試驗批准

恆瑞醫藥(600276.SH)：HRS-6719片獲准開展晚期實體瘤臨牀試驗

三生國健(688336.SH)：SSGJ-627注射液潰瘍性結腸炎(UC)I期臨牀試驗獲批准

康泰生物(300601.SZ)：四價腸道病毒滅活疫苗(Vero細胞)開啓Ⅰ期臨牀試驗

【康泰生物：四價腸道病毒滅活疫苗（Vero細胞）開啓Ⅰ期臨牀試驗】康泰生物公告，公司全資子公司北京民海生物科技有限公司研發的四價腸道病毒滅活疫苗（Vero細胞）已完成Ⅰ期臨牀試驗準備工作，開啓Ⅰ期臨牀試驗，並於近日成功完成首例受試者入組。該疫苗適用於6月齡至71月齡EV-A71、CV-A6、CV-A10、CV-A16易感者，可刺激機體產生抗EV-A71、CV-A6、CV-A10、CV-A16的免疫力，用於預防腸道病毒EV-A71、CV-A6、CV-A10、CV-A16感染所致的手足口病等傳染病。目前全球尚無四價腸道病毒滅活疫苗（Vero細胞）獲批上市。

泰格醫藥04月03日主力淨流入173萬元散户資金拋售

CXO企業國內營收集體“首降” 五大龍頭淨利潤全線下滑拐點漸顯至暗時刻已過？

復宏漢霖HLX04-O臨牀試驗達主要研究終點

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EGFR、c-Met结合阻断EGFR、c-Met信号通路，ADC经细胞内吞并转运到溶酶体，连接子经酶切后释放出DDDXD，导致DNA损伤和细胞死亡。","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":"http://www.zhitongcaijing.com/content/detail/1274157.html","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":"stock_zhitongcaijing","symbols":["ADC","BK4080","BK1589","BK1583","BK4017","03347","BK1515","CDE","BK4231","01177","BK1576","BK1521","BK1141","BK1191"],"gpt_icon":0},{"id":"2524261031","title":"中國生物製藥(01177)研發的抗腫瘤藥“TQB2101 (ROR1 ADC)”獲得NMPA的臨牀試驗默示許可","url":"https://stock-news.laohu8.com/highlight/detail?id=2524261031","media":"智通财经","labels":["productRelease"],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2524261031?lang=zh_tw&edition=fundamental","pubTime":"2025-04-03 22:53","pubTimestamp":1743692000,"startTime":"0","endTime":"0","summary":"智通财经APP讯，中国生物制药(01177)公布，该集团自主研发的“TQB2101 (ROR1 ADC)”已获得中国国家药品监督管理局(NMPA)的临床试验默示许可，拟用于治疗晚期恶性肿瘤。临床前研究数据显示，TQB2101在多种ROR1阳性肿瘤模型中展现出抗肿瘤活性，且具有良好的安全性特征。此次获批的I期临床试验将重点评估其在人体内的安全性、耐受性、药代动力学特性及初步疗效。","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":"http://www.zhitongcaijing.com/content/detail/1274155.html","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":"stock_zhitongcaijing","symbols":["BK4231","03347","BK1515","BK1576","BK1589","BK1141","BK1191","01177","BK4080","BK1583","ADC","BK1521"],"gpt_icon":0},{"id":"2524089265","title":"每日賣空追蹤 | 泰格醫藥 04月03日賣空量成交26.73萬股，賣空比例為11.86%","url":"https://stock-news.laohu8.com/highlight/detail?id=2524089265","media":"市场透视","labels":[],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2524089265?lang=zh_tw&edition=fundamental","pubTime":"2025-04-03 21:58","pubTimestamp":1743688720,"startTime":"0","endTime":"0","summary":"泰格医药北京时间04月03日，涨0.33%，卖空量成交26.73万股，较上一交易日减少23.45%更多个股卖空数据请看下面视窗：卖空数据是观测市场多空博弈的关键指标：短期可反映市场情绪，高卖空比例预示看空预期，但极端值可能触发轧空反弹；长期结合基本面恶化则预警下行风险。需注意其局限性：卖空行为包含对冲需求，未必单纯看空；机构可能通过衍生品做空未体现在数据中，且散户跟风易扭曲信号。股市有风险，请谨慎决策。","market":"hk","thumbnail":null,"type":0,"news_type":0,"thumbnails":[],"rights":{"source":"tencent","url":"http://gu.qq.com/resources/shy/news/detail-v2/index.html#/?id=nesSN20250403215845a6ae9efe&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, body","filters":".relate-stock, .hot-list, .recom-box, .wx-sou","directOrigin":true},"property":[],"language":"zh","translate_title":"","themeId":null,"theme_name":"","theme_type":"","isJumpTheme":false,"source_url":"http://gu.qq.com/resources/shy/news/detail-v2/index.html#/?id=nesSN20250403215845a6ae9efe&s=b","is_publish_highlight":false,"source_rank":0,"column":"","sentiment":"-1","news_top_title":null,"news_tag":"","news_rank":0,"length":0,"strategy_id":0,"source":"tencent","symbols":["BK1576","BK1583","03347","BK1141"],"gpt_icon":0},{"id":"2524258724","title":"石四藥集團SYN045片獲三種規格一期臨牀試驗許可","url":"https://stock-news.laohu8.com/highlight/detail?id=2524258724","media":"财中社","labels":[],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2524258724?lang=zh_tw&edition=fundamental","pubTime":"2025-04-03 19:26","pubTimestamp":1743679568,"startTime":"0","endTime":"0","summary":"4月3日，石四药集团（02005）发布公告，宣布其化学药品1类新药SYN045片已获得中国国家药品监督管理局新增三种不同规格（10mg、25mg及50mg）的一期临床试验许可。","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://finance.eastmoney.com/a/202504033364986654.html","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":"stock_eastmoney","symbols":["BK1141","BK1576","03347","BK1583","LU2460026573.USD","02005","BK1191"],"gpt_icon":0},{"id":"2524230781","title":"【石四藥集團(02005.HK)：SYN045片已取得國藥監局新增三種不同規格(10mg、25mg及50mg)的一期臨牀試驗許可】石四藥集團(02005.HK)發佈公告，該集團的化學藥品1類新藥SYN045片已取得中國國家藥品監督管理局新增三種不同規格(10mg、25mg及50mg)的一期臨牀試驗許可，可以滿足臨牀試驗多樣化需求，針對不同年齡段患者實現劑量梯度給藥，進一步優化精準給藥方案，提升SYN045片的臨牀應用價值。","url":"https://stock-news.laohu8.com/highlight/detail?id=2524230781","media":"金融界","labels":["productRelease"],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2524230781?lang=zh_tw&edition=fundamental","pubTime":"2025-04-03 19:12","pubTimestamp":1743678743,"startTime":"0","endTime":"0","summary":"石四药集团(02005.HK)发布公告，该集团的化学药品1类新药SYN045片已取得中国国家药品监督管理局新增三种不同规格(10mg、25mg及50mg)的一期临床试验许可，可以满足临床试验多样化需求，针对不同年龄段患者实现剂量梯度给药，进一步优化精准给药方案，提升SYN045片的临床应用价值。","market":"sh","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://24h.jrj.com.cn/2025/04/03191249285349.shtml","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":"jinrongjie_stock","symbols":["02005","BK1576","LU2460026573.USD","BK1141","BK1191","03347","BK1583"],"gpt_icon":0},{"id":"2524258205","title":"石四藥集團(02005)：SYN045片已取得國藥監局新增三種不同規格(10mg、25mg及50mg)的一期臨牀試驗許可","url":"https://stock-news.laohu8.com/highlight/detail?id=2524258205","media":"智通财经网","labels":["productRelease"],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2524258205?lang=zh_tw&edition=fundamental","pubTime":"2025-04-03 19:10","pubTimestamp":1743678600,"startTime":"0","endTime":"0","summary":"石四药集团发布公告，该集团的化学药品1类新药SYN045片已取得中国国家药品监督管理局新增三种不同规格的一期临床试验许可，可以满足临床试验多样化需求，针对不同年龄段患者实现剂量梯度给药，进一步优化精准给药方案，提升SYN045片的临床应用价值。SYN045为高度选择性PGI2受体激动剂。目前，在集团的临床前研究当中，SYN045具有良好的靶点选择性、化合物活性及安全性，在动物体内抗肺动脉高压效果明显，且其毒性低，有利于实现口服长期给药。","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":"https://finance.sina.com.cn/stock/hkstock/ggscyd/2025-04-03/doc-inerwwim2517511.shtml","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":"sina","symbols":["LU2460026573.USD","BK1141","03347","BK1583","02005","BK1191","BK1576"],"gpt_icon":0},{"id":"2524315472","title":"百誠醫藥(301096.SZ)創新藥BIOS-0618片獲臨牀試驗批准","url":"https://stock-news.laohu8.com/highlight/detail?id=2524315472","media":"智通财经","labels":["productRelease"],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2524315472?lang=zh_tw&edition=fundamental","pubTime":"2025-04-03 18:11","pubTimestamp":1743675096,"startTime":"0","endTime":"0","summary":"智通财经APP讯，百诚医药(301096.SZ)公告，公司近日收到国家药品监督管理局(NMPA)临床试验批准通知书，公司自主研发的创新药BIOS-0618片将开展临床试验研究。本品此前已获得适用于神经病理性疼痛治疗的临床试验批准，本次为新增适应症获批，新增适应症为：阻塞性睡眠呼吸暂停综合征(OSA)患者日间过度思睡。","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":"http://www.zhitongcaijing.com/content/detail/1273945.html","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":"stock_zhitongcaijing","symbols":["BK1574","06978","301096","BK1583","03347","BK0216","159992","BK1161","BK1576","BK1141"],"gpt_icon":0},{"id":"2524233720","title":"恆瑞醫藥(600276.SH)：HRS-6719片獲准開展晚期實體瘤臨牀試驗","url":"https://stock-news.laohu8.com/highlight/detail?id=2524233720","media":"智通财经","labels":["productRelease"],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2524233720?lang=zh_tw&edition=fundamental","pubTime":"2025-04-03 17:21","pubTimestamp":1743672116,"startTime":"0","endTime":"0","summary":"智通财经APP讯，恒瑞医药(600276.SH)公告，公司子公司山东盛迪医药有限公司、上海恒瑞医药有限公司收到国家药品监督管理局核准签发关于HRS-6719片的《药物临床试验批准通知书》，将于近期开展临床试验(晚期实体瘤)。","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":"http://www.zhitongcaijing.com/content/detail/1273893.html","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":"stock_zhitongcaijing","symbols":["LU1969619763.USD","LU2488822045.USD","BK0028","LU2148510915.USD","BK0239","LU1328615791.USD","BK1576","BK0060","03347","BK0188","BK1141","LU2328871848.SGD","BK1583","LU1064130708.USD","LU0405327148.USD","BK0183","600276","LU0405327494.USD","LU1064131003.USD","BK0012","BK0196"],"gpt_icon":0},{"id":"2524238731","title":"三生國健(688336.SH)：SSGJ-627注射液潰瘍性結腸炎(UC)I期臨牀試驗獲批准","url":"https://stock-news.laohu8.com/highlight/detail?id=2524238731","media":"智通财经","labels":["dataReport"],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2524238731?lang=zh_tw&edition=fundamental","pubTime":"2025-04-03 17:17","pubTimestamp":1743671855,"startTime":"0","endTime":"0","summary":"智通财经APP讯，三生国健(688336.SH)公告，公司SSGJ-627注射液收到国家药品监督管理局核准签发的《药物临床试验批准通知书》，同意公司开展SSGJ-627注射液溃疡性结肠炎(UC)的I期临床试验。","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://www.zhitongcaijing.com/content/detail/1273892.html","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":"stock_zhitongcaijing","symbols":["BK1576","BK1141","03347","BK0239","BK1583","688336"],"gpt_icon":0},{"id":"2524282731","title":"康泰生物(300601.SZ)：四價腸道病毒滅活疫苗(Vero細胞)開啓Ⅰ期臨牀試驗","url":"https://stock-news.laohu8.com/highlight/detail?id=2524282731","media":"智通财经","labels":["productRelease"],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2524282731?lang=zh_tw&edition=fundamental","pubTime":"2025-04-03 16:47","pubTimestamp":1743670041,"startTime":"0","endTime":"0","summary":"智通财经APP讯，康泰生物(300601.SZ)公告，公司全资子公司北京民海生物科技有限公司(简称“民海生物”)研发的四价肠道病毒灭活疫苗(Vero细胞)已完成Ⅰ期临床试验准备工作，开启Ⅰ期临床试验，并于近日成功完成首例受试者入组。公告显示，四价肠道病毒灭活疫苗(Vero细胞)Ⅰ期临床试验采取部分随机、盲态、阳性对照试验设计，旨在评价其在6月龄及以上健康人群中的安全性和初步免疫原性。","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":"http://www.zhitongcaijing.com/content/detail/1273854.html","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":"stock_zhitongcaijing","symbols":["BK0046","BK1583","BK1141","BK0239","03347","300601","BK1576","BK0201"],"gpt_icon":0},{"id":"2524824802","title":"【康泰生物：四價腸道病毒滅活疫苗（Vero細胞）開啓Ⅰ期臨牀試驗】康泰生物公告，公司全資子公司北京民海生物科技有限公司研發的四價腸道病毒滅活疫苗（Vero細胞）已完成Ⅰ期臨牀試驗準備工作，開啓Ⅰ期臨牀試驗，並於近日成功完成首例受試者入組。該疫苗適用於6月齡至71月齡EV-A71、CV-A6、CV-A10、CV-A16易感者，可刺激機體產生抗EV-A71、CV-A6、CV-A10、CV-A16的免疫力，用於預防腸道病毒EV-A71、CV-A6、CV-A10、CV-A16感染所致的手足口病等傳染病。目前全球尚無四價腸道病毒滅活疫苗（Vero細胞）獲批上市。","url":"https://stock-news.laohu8.com/highlight/detail?id=2524824802","media":"金融界","labels":["productRelease"],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2524824802?lang=zh_tw&edition=fundamental","pubTime":"2025-04-03 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