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泰格醫藥

50.600

-0.500-0.98%

成交量：286.84萬

成交額：1.45億

市值：435.67億

市盈率：98.47

高：52.450

開：51.150

低：49.600

收：51.100

資料載入中...

總覽公司新聞公告

【微芯生物：CS231295臨牀試驗申請獲FDA受理】微芯生物公告，公司全資子公司微芯生物科技（美國）有限公司於2025年6月30日收到美國食品藥品監督管理局（FDA）的書面回覆，自主研發的CS231295關於晚期實體瘤的臨牀試驗申請獲得FDA受理。受理號為IND176942，受理日期為2025年6月30日，適應症為晚期實體瘤，申請事項為新藥臨牀試驗申請。CS231295作為透腦AuroraB選擇性抑制劑，目前全球尚無同類設計的藥物進入臨牀試驗階段。

昂利康：目前在研的創新藥項目僅有一個

海正藥業：收到HS387片臨牀試驗批准通知書

安科生物：公司AK2024注射液獲得藥物臨牀試驗批准

安科生物(300009.SZ)：AK2024注射液臨牀試驗獲批准

安科生物：AK2024注射液獲藥物臨牀試驗批准

兩部門：探索為創新藥研發提供必要的醫保數據服務

国家医保局

慧與漲12.6%瞻博網絡漲8.4%司法部已就其對慧與以 140 億美元收購瞻博網絡的訴訟達成和解。Moderna漲3.3

【華東醫藥：全資子公司獲得美國FDA新藥臨牀試驗批准通知】華東醫藥6月30日公告，全資子公司杭州中美華東製藥有限公司收到美國食品藥品監督管理局通知，由中美華東申報的注射用HDM2012藥品臨牀試驗申請已獲得美國FDA批准，可在美國開展I期臨牀試驗，適應症為晚期實體瘤。

【興證全球基金增持泰格醫藥(03347.HK)30.03萬股每股作價約35.66港元】智通財經APP獲悉，香港聯交所最

【康弘藥業：子公司收到KH813注射液臨牀試驗批准通知書】康弘藥業(002773.SZ)公告稱，公司全資子公司成都康弘生物科技有限公司收到國家藥品監督管理局簽發的《藥物臨牀試驗批准通知書》，同意KH813注射液按生物類似藥開展臨牀試驗。KH813注射液是康弘生物研發的帕博利珠單抗生物類似藥，主要用於治療多種晚期實體瘤。由於藥品研發存在不確定性，投資者需謹慎決策並注意投資風險。

【Moderna美股盤前漲超6%】Moderna美股盤前漲超6%，此前公司宣佈實驗性流感疫苗達到三期臨牀試驗主要終點。

Moderna美股盤前漲超6%此前公司宣佈實驗性流感疫苗達到三期臨牀試驗主要終點。

Moderna(MRNA.US)盤前漲超5%

羅氏、科倫博泰、加科思等熱議創新藥臨牀試驗“30日通道”

医药经济报

每日賣空追蹤 | 泰格醫藥 06月30日賣空量成交22.69萬股，賣空比例為3.74%

江蘇康緣藥業股份有限公司藥品申請臨牀試驗默示許可獲受理

重慶華森製藥股份有限公司藥品申請臨牀試驗默示許可獲受理

【港股異動 | CRO概念股持續走高新藥臨牀試驗加速利好CRO企業機構稱板塊補漲動力充足】智通財經APP獲悉，CRO

港股異動 | CRO概念股持續走高新藥臨牀試驗加速利好CRO企業機構稱板塊補漲動力充足

智通财经网

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