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康希諾生物:自願公告 - 關於獲得13價肺炎球菌多糖結合疫苗(CRM197,TT載體)III期臨床試驗總結報告的公告

CANSINOBIO: VOLUNTARY ANNOUNCEMENT - OBTAINING THE FINAL REPORT OF PHASE III CLINICAL TRIAL OF 13-VALENT PNEUMOCOCCAL CONJUGATE VACCINE (CRM197, TT VECTOR)

香港交易所 ·  Jan 30 19:04
Summary by Futu AI
康希諾生物股份公司宣布其開發的13價肺炎球菌多糖結合疫苗(PCV13i)近日獲得III期臨床試驗總結報告。該疫苗採用創新的多糖抗原與蛋白載體共價結合技術,能在嬰幼兒體內誘導高特異性抗體水平並產生免疫記憶。III期臨床試驗結果顯示PCV13i具有良好的安全性和免疫原性,已達到預設的臨床終點。本公司將根據試驗結果向國家藥品監督管理局遞交藥品生產註冊申請,並需經過後續審評和檢查程序,方可進行產品上市。董事會呼籲股東及潛在投資者買賣股份時應審慎行事。公告由董事長Xuefeng YU於2024年1月30日發布。
康希諾生物股份公司宣布其開發的13價肺炎球菌多糖結合疫苗(PCV13i)近日獲得III期臨床試驗總結報告。該疫苗採用創新的多糖抗原與蛋白載體共價結合技術,能在嬰幼兒體內誘導高特異性抗體水平並產生免疫記憶。III期臨床試驗結果顯示PCV13i具有良好的安全性和免疫原性,已達到預設的臨床終點。本公司將根據試驗結果向國家藥品監督管理局遞交藥品生產註冊申請,並需經過後續審評和檢查程序,方可進行產品上市。董事會呼籲股東及潛在投資者買賣股份時應審慎行事。公告由董事長Xuefeng YU於2024年1月30日發布。
Conchino Biologics Corporation announced the recent receipt of the Phase III clinical trial summary report for its development of the 13-price pneumococcal polyglucose-coupled vaccine (PCV13i). The vaccine uses innovative polyglycemic antigen and protein carrier co-binding technology to induce high levels of specific antibodies in infants and young children and generate immune memories. Phase III clinical trial results show that PCV13i has good safety and immunogenicity and has reached the default clinical endpoint. The Company will submit a production registration application to the National Drug Administration based on the results of the trial and will be subject to subsequent review and inspection procedures in order to place the product on the market. The Board urges shareholders and potential investors to exercise caution when trading shares. The announcement was issued by Chairman Xuefeng YU on January 30, 2024.
Conchino Biologics Corporation announced the recent receipt of the Phase III clinical trial summary report for its development of the 13-price pneumococcal polyglucose-coupled vaccine (PCV13i). The vaccine uses innovative polyglycemic antigen and protein carrier co-binding technology to induce high levels of specific antibodies in infants and young children and generate immune memories. Phase III clinical trial results show that PCV13i has good safety and immunogenicity and has reached the default clinical endpoint. The Company will submit a production registration application to the National Drug Administration based on the results of the trial and will be subject to subsequent review and inspection procedures in order to place the product on the market. The Board urges shareholders and potential investors to exercise caution when trading shares. The announcement was issued by Chairman Xuefeng YU on January 30, 2024.

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