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康方生物:自願公告 - AK112 -303 /HARMONi-2已作為LBA入選2024 WCLC將在全體會議主席專題研討會上口頭報告

AKESO: VOLUNTARY ANNOUNCEMENT - AK112-303/HARMONI-2 WAS ACCEPTED AS LBA OF 2024 WCLCPRESIDENTIAL SYMPOSIUM ORAL PRESENTATION

HKEX ·  Aug 12 07:42

Summary by Futu AI

康方生物科技(開曼)有限公司宣布,其自主研發的雙特異性抗體依達方®(依沃西,PD-1/VEGF)用於治療PD-L1表達陽性的非小細胞肺癌的III期臨床研究AK112-303/HARMONi-2的結果,已被選為2024年世界肺癌大會的Late-Breaking Abstract,並將由主要研究者周彩存教授在會議上口頭報告。依沃西在III期臨床研究中顯示療效顯著優於帕博利珠單抗,公司已向中國國家藥品監督管理局遞交新適應症上市申請。依沃西目前在中國已獲批一項適應症,並有多項III期臨床研究正在進行,包括國際多中心試驗和16個不同適應症的臨床試驗。該消息於2024年8月12日由公司主席兼執行董事夏瑜博士發布。
康方生物科技(開曼)有限公司宣布,其自主研發的雙特異性抗體依達方®(依沃西,PD-1/VEGF)用於治療PD-L1表達陽性的非小細胞肺癌的III期臨床研究AK112-303/HARMONi-2的結果,已被選為2024年世界肺癌大會的Late-Breaking Abstract,並將由主要研究者周彩存教授在會議上口頭報告。依沃西在III期臨床研究中顯示療效顯著優於帕博利珠單抗,公司已向中國國家藥品監督管理局遞交新適應症上市申請。依沃西目前在中國已獲批一項適應症,並有多項III期臨床研究正在進行,包括國際多中心試驗和16個不同適應症的臨床試驗。該消息於2024年8月12日由公司主席兼執行董事夏瑜博士發布。
Kangfang Biotech (Cayman) Co., Ltd. announced that its self-developed bispecific antibody Idafoxi (Ivosidenib, PD-1/VEGF) used in the phase III clinical trial AK112-303/HARMONi-2 for the treatment of PD-L1 positive non-small cell lung cancer has been selected as a late-breaking abstract for the 2024 World Lung Cancer Conference and will be orally presented by the principal investigator Professor Zhou Caicun. Idafoxi showed significant efficacy in the phase III clinical trial and performed better than Pembrolizumab. The company has submitted a new indication application to the China National Medical Products Administration. Idafoxi currently has one indication approved in China, and multiple phase III clinical trials are underway, including international multicenter trials and clinical trials for 16 different indications. This news was released by the company's Chairman and Executive Director Dr. Xia Yu on August 12, 2024.
Kangfang Biotech (Cayman) Co., Ltd. announced that its self-developed bispecific antibody Idafoxi (Ivosidenib, PD-1/VEGF) used in the phase III clinical trial AK112-303/HARMONi-2 for the treatment of PD-L1 positive non-small cell lung cancer has been selected as a late-breaking abstract for the 2024 World Lung Cancer Conference and will be orally presented by the principal investigator Professor Zhou Caicun. Idafoxi showed significant efficacy in the phase III clinical trial and performed better than Pembrolizumab. The company has submitted a new indication application to the China National Medical Products Administration. Idafoxi currently has one indication approved in China, and multiple phase III clinical trials are underway, including international multicenter trials and clinical trials for 16 different indications. This news was released by the company's Chairman and Executive Director Dr. Xia Yu on August 12, 2024.

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