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CRISPR Therapeutics | 10-Q: Quarterly report

CRISPR Therapeutics | 10-Q: Quarterly report

CRISPR Therapeutics | 10-Q:季度報表
美股sec公告 ·  05/08 16:29
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CRISPR Therapeutics, a leading gene editing company, has reported significant financial and business developments in its latest quarterly report. Financially, the company has issued 1.5 million common shares under the 2021 ATM at an average price of $139.28 per share, resulting in aggregate proceeds of $212.4 million net of equity issuance costs. Additionally, CRISPR Therapeutics entered into a registered direct offering in February 2024, selling approximately $280.0 million of its common shares at $71.50 per share, with net proceeds of $279.0 million. The company did not generate material revenue for the quarter ended March 31, 2024, compared to $100.0 million in the same period the previous year, primarily from an upfront payment from Vertex. Research and development expenses decreased to $76.2 million from $99.9 million year-on-year, while general and administrative expenses...Show More
CRISPR Therapeutics, a leading gene editing company, has reported significant financial and business developments in its latest quarterly report. Financially, the company has issued 1.5 million common shares under the 2021 ATM at an average price of $139.28 per share, resulting in aggregate proceeds of $212.4 million net of equity issuance costs. Additionally, CRISPR Therapeutics entered into a registered direct offering in February 2024, selling approximately $280.0 million of its common shares at $71.50 per share, with net proceeds of $279.0 million. The company did not generate material revenue for the quarter ended March 31, 2024, compared to $100.0 million in the same period the previous year, primarily from an upfront payment from Vertex. Research and development expenses decreased to $76.2 million from $99.9 million year-on-year, while general and administrative expenses also saw a reduction. CRISPR Therapeutics continues to advance its gene editing technology, with the landmark approval of its CRISPR-based therapy, CASGEVY, for severe sickle cell disease and transfusion-dependent beta thalassemia. The company is also progressing in multiple therapeutic areas, including immuno-oncology, autoimmune diseases, and type 1 diabetes. Looking ahead, CRISPR Therapeutics plans to initiate clinical trials for CTX112 in systemic lupus erythematosus and CTX131 in hematologic malignancies in the first half of 2024. The company's liquidity position remains strong with $2,108.1 million in cash, cash equivalents, and marketable securities as of March 31, 2024.
領先的基因編輯公司CRISPR Therapeutics在其最新的季度報告中報告了重大的財務和業務發展。財務方面,該公司已在2021年自動櫃員機下發行了150萬股普通股,平均價格爲每股139.28美元,扣除股票發行成本後的總收益爲2.124億美元。此外,CRISPR Therapeutics於2024年2月進行了註冊直接發行,以每股71.50美元的價格出售了約2.8億美元的普通股,淨收益爲2.790億美元。該公司在截至2024年3月31日的季度中沒有產生實質性收入,而去年同期爲1.00億美元,主要來自Vertex的預付款。研發費用從同比的9,990萬美元降至7,620萬美元,而一般和管理費用也...展開全部
領先的基因編輯公司CRISPR Therapeutics在其最新的季度報告中報告了重大的財務和業務發展。財務方面,該公司已在2021年自動櫃員機下發行了150萬股普通股,平均價格爲每股139.28美元,扣除股票發行成本後的總收益爲2.124億美元。此外,CRISPR Therapeutics於2024年2月進行了註冊直接發行,以每股71.50美元的價格出售了約2.8億美元的普通股,淨收益爲2.790億美元。該公司在截至2024年3月31日的季度中沒有產生實質性收入,而去年同期爲1.00億美元,主要來自Vertex的預付款。研發費用從同比的9,990萬美元降至7,620萬美元,而一般和管理費用也有所減少。CRISPR Therapeutics繼續推進其基因編輯技術,其基於CRISPR的治療方法CASGEVY獲得了具有里程碑意義的批准,該療法用於嚴重的鐮狀細胞病和輸血依賴性β地中海貧血。該公司還在多個治療領域取得進展,包括免疫腫瘤學、自身免疫性疾病和1型糖尿病。展望未來,CRISPR Therapeutics計劃在2024年上半年啓動針對系統性紅斑狼瘡的 CTX112 和用於血液系統惡性腫瘤的 CTX131 的臨床試驗。該公司的流動性狀況仍然強勁,截至2024年3月31日,現金、現金等價物和有價證券爲21.081億美元。
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