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CRISPR Therapeutics | 8-K: CRISPR Therapeutics Provides Business Update and Reports Third Quarter 2024 Financial Results

CRISPR Therapeutics | 8-K: CRISPR Therapeutics Provides Business Update and Reports Third Quarter 2024 Financial Results

CRISPR Therapeutics | 8-K:CRISPR Therapeutics提供最新業務並公佈2024年第三季度財務業績
美股SEC公告 ·  2024/11/05 22:06

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CRISPR Therapeutics reported Q3 2024 financial results with a strong cash position of $1.94 billion as of September 30, 2024. The company's flagship product CASGEVY received additional approvals in Switzerland and Canada for treating sickle cell disease and transfusion-dependent beta thalassemia in patients 12 years and older. As of mid-October, 45 authorized treatment centers have been activated globally with approximately 40 patients having completed cell collection.The company's clinical pipeline continues to advance, with promising preliminary data from CTX112, their next-generation CD19 CAR-T therapy, showing a 67% overall response rate in lymphoma patients. Two clinical trials are ongoing for CTX131 targeting CD70 in solid tumors and hematological malignancies. Additionally, in vivo programs CTX310 and CTX320 for cardiovascular diseases are progressing in clinical trials.Q3 financial results showed R&D expenses of $82.2 million, down from $90.7 million year-over-year, and a net loss of $85.9 million compared to $112.2 million in Q3 2023. The company's strong balance sheet was bolstered by a $280 million offering and a $200 million milestone payment from Vertex Pharmaceuticals following CASGEVY's approval.
CRISPR Therapeutics reported Q3 2024 financial results with a strong cash position of $1.94 billion as of September 30, 2024. The company's flagship product CASGEVY received additional approvals in Switzerland and Canada for treating sickle cell disease and transfusion-dependent beta thalassemia in patients 12 years and older. As of mid-October, 45 authorized treatment centers have been activated globally with approximately 40 patients having completed cell collection.The company's clinical pipeline continues to advance, with promising preliminary data from CTX112, their next-generation CD19 CAR-T therapy, showing a 67% overall response rate in lymphoma patients. Two clinical trials are ongoing for CTX131 targeting CD70 in solid tumors and hematological malignancies. Additionally, in vivo programs CTX310 and CTX320 for cardiovascular diseases are progressing in clinical trials.Q3 financial results showed R&D expenses of $82.2 million, down from $90.7 million year-over-year, and a net loss of $85.9 million compared to $112.2 million in Q3 2023. The company's strong balance sheet was bolstered by a $280 million offering and a $200 million milestone payment from Vertex Pharmaceuticals following CASGEVY's approval.
CRISPR Therapeutics公佈了2024年第三季度的財務結果,截止到2024年9月30日,公司擁有強勁的現金儲備19.4億美金。公司的旗艦產品CASGEVY在瑞士和加拿大獲得了額外批准,用於治療12歲及以上患者的鐮狀細胞病和依賴輸血的β地中海貧血。截至10月中旬,全球已激活45個授權治療中心,大約40名患者已完成電芯採集。公司的臨牀管道持續推進,其下一代CD19 CAR-T療法CTX112的初步數據令人鼓舞,顯示淋巴瘤患者的總體應答率爲67%。目前正在進行兩項針對CD70的臨牀試驗,目標是治療實體腫瘤和血液惡性腫瘤。此外,心血管疾病的體內項目CTX310和CTX320也在進行臨牀試...展開全部
CRISPR Therapeutics公佈了2024年第三季度的財務結果,截止到2024年9月30日,公司擁有強勁的現金儲備19.4億美金。公司的旗艦產品CASGEVY在瑞士和加拿大獲得了額外批准,用於治療12歲及以上患者的鐮狀細胞病和依賴輸血的β地中海貧血。截至10月中旬,全球已激活45個授權治療中心,大約40名患者已完成電芯採集。公司的臨牀管道持續推進,其下一代CD19 CAR-T療法CTX112的初步數據令人鼓舞,顯示淋巴瘤患者的總體應答率爲67%。目前正在進行兩項針對CD70的臨牀試驗,目標是治療實體腫瘤和血液惡性腫瘤。此外,心血管疾病的體內項目CTX310和CTX320也在進行臨牀試驗。第三季度財務結果顯示,研發費用爲8220萬美金,較去年同期的9070萬美金有所下降,淨虧損爲8590萬美金,相比2023年第三季度的11220萬美金有所減少。公司的強勁資產負債表得益於28000萬美金的募資和福泰製藥在CASGEVY獲批後支付的20000萬美金里程碑款項。
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