國鼎新藥國際授權首發! - 股票
By Oscar
at 2020-08-06T21:38
at 2020-08-06T21:38
Table of Contents
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1.發文前請先詳閱[新聞]分類發文規範,未依規範發文將受處份。
2.連結過長請善用 https://goo.gl/ 縮網址,連結能不能點擊者板規1-2-2處份。
3.心得/評論請盡量充實,心得過短或濫竽充數將會以1-2-3&一行文規範水桶處份。
---------------------------按ctrl+y可刪除以上內容。----------------------
1.原文連結:
https://m.ctee.com.tw/livenews/aj/a89453002020080620181292
2.原文內容:
國鼎國際授權首發 新冠肺炎新藥簽定韓國授權合作
國鼎生技(4132)宣布與韓國BNC Korea Co., Ltd.簽訂共同開發用於治療新型冠狀病毒
肺炎(Covid-19)新藥Antroquinonol(Hocena)之合作意向書,契約或承諾起迄日為109
年8月6日至12月31日。國鼎表示,與BNK後續的合約將會說明有關授權金與產量供應的細
節。此次只是區域授權的開端,在尚未開始臨床試驗,就有授權金,創歷史意義。
國鼎生技將其自行研發之小分子新藥Antroquinonol(Hocena)授權予 BNC Korea Co., L
td.,並由BNC Korea Co., Ltd.負責進行韓國境內臨床試驗及新藥上市之申請;藉由與BN
C Korea Co., Ltd.之共同合作,將有助拓展新型冠狀病毒肺炎(Covid-19)新藥Antroqu
inonol(Hocena)之東亞地區佈局。另透過與BNC Korea Co., Ltd.之共合作,拓展國鼎
開發之新型冠狀病毒肺炎(Covid-19)新藥Antroquinonol(Hocena)之韓國市場。
此外,國鼎通過美國食品藥物管理局(FDA)的新藥臨床(IND)審查,獲准在美國執行研
發中新藥Antroquinonol(HOCENA)治療新型冠狀病毒肺炎(Covid-19)患者的二期人體
安全性與功效性臨床試驗,成為台灣唯一獲 FDA核准進入美國新冠肺炎二期人體臨床的新
藥。
國鼎指出,目前已完成今年第一波私募;若一切順利,最快將於今年底完成收案,並進行
資料分析,後續相關試驗若達顯著功效,將進行美國緊急使用授(EUA)之申請。該小分
子新藥為國鼎生技所研發,擁有100%專利,後續完成相關之臨床試驗並獲得核准即可上市
。
3.心得/評論:
上次30幾進場,在63獲利了結,這次國內疫情升溫下,是否能再帶動生技股一波高潮?國
鼎新藥還未臨床結束就與韓國簽訂授權,美國衛生部長即將來台,是否國鼎能從中再有好
消息發出?大家敬請期待,興櫃股風險較大,單純分享新聞,投資自負盈虧。
--
1.發文前請先詳閱[新聞]分類發文規範,未依規範發文將受處份。
2.連結過長請善用 https://goo.gl/ 縮網址,連結能不能點擊者板規1-2-2處份。
3.心得/評論請盡量充實,心得過短或濫竽充數將會以1-2-3&一行文規範水桶處份。
---------------------------按ctrl+y可刪除以上內容。----------------------
1.原文連結:
https://m.ctee.com.tw/livenews/aj/a89453002020080620181292
2.原文內容:
國鼎國際授權首發 新冠肺炎新藥簽定韓國授權合作
國鼎生技(4132)宣布與韓國BNC Korea Co., Ltd.簽訂共同開發用於治療新型冠狀病毒
肺炎(Covid-19)新藥Antroquinonol(Hocena)之合作意向書,契約或承諾起迄日為109
年8月6日至12月31日。國鼎表示,與BNK後續的合約將會說明有關授權金與產量供應的細
節。此次只是區域授權的開端,在尚未開始臨床試驗,就有授權金,創歷史意義。
國鼎生技將其自行研發之小分子新藥Antroquinonol(Hocena)授權予 BNC Korea Co., L
td.,並由BNC Korea Co., Ltd.負責進行韓國境內臨床試驗及新藥上市之申請;藉由與BN
C Korea Co., Ltd.之共同合作,將有助拓展新型冠狀病毒肺炎(Covid-19)新藥Antroqu
inonol(Hocena)之東亞地區佈局。另透過與BNC Korea Co., Ltd.之共合作,拓展國鼎
開發之新型冠狀病毒肺炎(Covid-19)新藥Antroquinonol(Hocena)之韓國市場。
此外,國鼎通過美國食品藥物管理局(FDA)的新藥臨床(IND)審查,獲准在美國執行研
發中新藥Antroquinonol(HOCENA)治療新型冠狀病毒肺炎(Covid-19)患者的二期人體
安全性與功效性臨床試驗,成為台灣唯一獲 FDA核准進入美國新冠肺炎二期人體臨床的新
藥。
國鼎指出,目前已完成今年第一波私募;若一切順利,最快將於今年底完成收案,並進行
資料分析,後續相關試驗若達顯著功效,將進行美國緊急使用授(EUA)之申請。該小分
子新藥為國鼎生技所研發,擁有100%專利,後續完成相關之臨床試驗並獲得核准即可上市
。
3.心得/評論:
上次30幾進場,在63獲利了結,這次國內疫情升溫下,是否能再帶動生技股一波高潮?國
鼎新藥還未臨床結束就與韓國簽訂授權,美國衛生部長即將來台,是否國鼎能從中再有好
消息發出?大家敬請期待,興櫃股風險較大,單純分享新聞,投資自負盈虧。
--
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