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藥明巨諾-B:截至2024年12月31日止年度之年度業績公告

JW THERAP-B: ANNUAL RESULTS ANNOUNCEMENT FOR THE YEAR ENDED DECEMBER 31, 2024

HKEX ·  Mar 27 10:24

Summary by Moomoo AI

藥明巨諾2024年度營業收入為人民幣1.58億元,同比下降9%,毛利率為48.9%。年內虧損收窄至人民幣5.91億元,較2023年的7.68億元減少23.1%。虧損收窄主要得益於研發開支同比減少31.6%至2.83億元,以及一般行政開支下降14.2%至1.20億元。公司在細胞免疫治療領域取得多項進展,倍諾達®已獲批三項適應症。2024年8月獲批用於治療r/r MCL成人患者,成為中國首個獲批治療該適應症的細胞治療產品。此外,公司完成了倍諾達®用於二線LBCL治療的臨床試驗患者入組,計劃於2025年上半年提交新藥申請。公司持續推進產品管線開發,在血液惡性腫瘤、實體瘤及自身免疫疾病等領域均有進展。於2024年啟動了多個創新項目的臨床開發,包括針對MAGE-A4及DLL3的細胞治療產品。同時,公司通過優化生產工藝、採購國產原材料等措施,持續推進成本控制,截至年底銀行結餘及現金為人民幣7.57億元。
藥明巨諾2024年度營業收入為人民幣1.58億元,同比下降9%,毛利率為48.9%。年內虧損收窄至人民幣5.91億元,較2023年的7.68億元減少23.1%。虧損收窄主要得益於研發開支同比減少31.6%至2.83億元,以及一般行政開支下降14.2%至1.20億元。公司在細胞免疫治療領域取得多項進展,倍諾達®已獲批三項適應症。2024年8月獲批用於治療r/r MCL成人患者,成為中國首個獲批治療該適應症的細胞治療產品。此外,公司完成了倍諾達®用於二線LBCL治療的臨床試驗患者入組,計劃於2025年上半年提交新藥申請。公司持續推進產品管線開發,在血液惡性腫瘤、實體瘤及自身免疫疾病等領域均有進展。於2024年啟動了多個創新項目的臨床開發,包括針對MAGE-A4及DLL3的細胞治療產品。同時,公司通過優化生產工藝、採購國產原材料等措施,持續推進成本控制,截至年底銀行結餘及現金為人民幣7.57億元。
In 2024, WuXi AppTec's revenue is 0.158 billion yuan, a decrease of 9% year-on-year, with a gross margin of 48.9%. The annual loss narrowed to 0.591 billion yuan, a reduction of 23.1% compared to 0.768 billion yuan in 2023. The loss reduction is mainly due to a 31.6% decrease in R&D spending to 0.283 billion yuan, and a 14.2% decrease in general administrative expenses to 0.12 billion yuan.The company has made multiple advancements in the field of cell immunotherapy, with Benauda® approved for three indications. In August 2024, it was approved for the treatment of adult patients with r/r MCL, becoming the first cell therapy product approved in China for this indication. Additionally, the company completed patient enrollment for clinical trials of Benauda® for second-line LBCL...Show More
In 2024, WuXi AppTec's revenue is 0.158 billion yuan, a decrease of 9% year-on-year, with a gross margin of 48.9%. The annual loss narrowed to 0.591 billion yuan, a reduction of 23.1% compared to 0.768 billion yuan in 2023. The loss reduction is mainly due to a 31.6% decrease in R&D spending to 0.283 billion yuan, and a 14.2% decrease in general administrative expenses to 0.12 billion yuan.The company has made multiple advancements in the field of cell immunotherapy, with Benauda® approved for three indications. In August 2024, it was approved for the treatment of adult patients with r/r MCL, becoming the first cell therapy product approved in China for this indication. Additionally, the company completed patient enrollment for clinical trials of Benauda® for second-line LBCL treatment, with plans to submit a New Drug Application in the first half of 2025.The company continues to advance its product pipeline development, making progress in hematological malignancies, solid tumors, and autoimmune diseases. In 2024, multiple innovative clinical development projects were initiated, including cell therapy products targeting MAGE-A4 and DLL3. Meanwhile, the company is continuously pushing cost control measures through the optimization of production processes and procurement of domestic raw materials, with a year-end bank balance and cash of 0.757 billion yuan.
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