港股詳情

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泰格醫藥

51.100

+0.6501.29%

成交量：559.00萬

成交額：2.87億

市值：439.97億

市盈率：99.62

高：52.500

開：51.800

低：50.400

收：50.450

資料載入中...

總覽公司新聞公告

【港股異動 | 雲頂新耀(01952.HK)漲超4% 宣佈EVER001治療原發性膜性腎病臨牀試驗數據取得積極結果】智通

盤前公告淘金：微芯生物臨牀試驗獲FDA受理、華菱線纜中標4.56億電力新能源項目，千里科技6月新能源車銷量增長74.11%

加科思-B(01167)完成泛KRAS抑制劑JAB-23E73 I/IIa期臨牀試驗在美國的首例患者給藥

【加科思-B(01167.HK)完成泛KRAS抑制劑JAB-23E73 I/IIa期臨牀試驗在美國的首例患者給藥】智通財

【美股異動 | 醫藥板塊逆市走高 Moderna(MRNA.US)漲超1.6%】智通財經APP獲悉，週二，美股醫藥板塊逆

雲頂新耀宣佈治療原發性膜性腎病的新型BTK抑制劑EVER001在1b/2a期臨牀試驗最新階段性數據，持續展現優異的有效性與安全性

7月1日界面新聞記者獲悉賽諾菲將對天演藥業進行戰略投資並啓動雙方SAFEbody安全抗體合作框架下的第三個SAFEbod

微芯生物：CS231295臨牀試驗申請獲FDA受理

【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。

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