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Regeneron Pharmaceuticals | 8-K: Regeneron Reports Third Quarter 2024 Financial and Operating Results

Regeneron Pharmaceuticals | 8-K: Regeneron Reports Third Quarter 2024 Financial and Operating Results

再生元製藥公司 | 8-K:Regeneron 公佈2024年第三季度財務和經營業績
美股SEC公告 ·  2024/10/31 04:15

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Regeneron reported robust Q3 2024 financial results with total revenues increasing 11% to $3.72 billion. Dupixent global net sales surged 23% to $3.82 billion, while U.S. EYLEA franchise sales grew 3% to $1.54 billion. GAAP diluted EPS rose 30% to $11.54, and non-GAAP diluted EPS increased 8% to $12.46.The company achieved significant regulatory milestones, including FDA approval of Dupixent as the first biologic therapy for COPD with an eosinophilic phenotype. Positive results were reported from pivotal trials in chronic spontaneous urticaria and bullous pemphigoid, with regulatory submissions planned. The company's clinical portfolio expanded to approximately 40 product candidates.Regeneron maintained strong financial position with $18.3 billion in cash and marketable securities. The company continued its share repurchase program, with $2.9 billion remaining available. R&D investments increased 18% to support pipeline advancement, particularly in late-stage oncology programs.
Regeneron reported robust Q3 2024 financial results with total revenues increasing 11% to $3.72 billion. Dupixent global net sales surged 23% to $3.82 billion, while U.S. EYLEA franchise sales grew 3% to $1.54 billion. GAAP diluted EPS rose 30% to $11.54, and non-GAAP diluted EPS increased 8% to $12.46.The company achieved significant regulatory milestones, including FDA approval of Dupixent as the first biologic therapy for COPD with an eosinophilic phenotype. Positive results were reported from pivotal trials in chronic spontaneous urticaria and bullous pemphigoid, with regulatory submissions planned. The company's clinical portfolio expanded to approximately 40 product candidates.Regeneron maintained strong financial position with $18.3 billion in cash and marketable securities. The company continued its share repurchase program, with $2.9 billion remaining available. R&D investments increased 18% to support pipeline advancement, particularly in late-stage oncology programs.
Regeneron公佈了2024年第三季度的強勁財務業績,總收入增長了11%,達到了37.2億美元。Dupixent全球淨銷售額猛增23%,達到了38.2億美元,而美國EYLEA業務的銷售額增長了3%,達到了15.4億美元。GAAP攤薄後每股收益增長了30%,達到了11.54美元,非GAAP攤薄後每股收益增長了8%,達到了12.46美元。公司達成了重要的監管里程碑,包括FDA批准Dupixent作爲首個用於治療具有嗜酸性表型的COPD的生物治療藥物。從慢性自發性蕁麻疹和水皰性天皰瘡的重要試驗中報告了積極的結果,並計劃進行監管提交。公司的臨牀投資組合擴展到大約40個產品候選。Regeneron保持了強勁的財務狀況,擁有183億美元的現金和可出售證券。公司持續進行股票回購計劃,剩餘29億美元可用。研發投資增長了18%,以支持管道的推進,特別是在晚期腫瘤項目上。
Regeneron公佈了2024年第三季度的強勁財務業績,總收入增長了11%,達到了37.2億美元。Dupixent全球淨銷售額猛增23%,達到了38.2億美元,而美國EYLEA業務的銷售額增長了3%,達到了15.4億美元。GAAP攤薄後每股收益增長了30%,達到了11.54美元,非GAAP攤薄後每股收益增長了8%,達到了12.46美元。公司達成了重要的監管里程碑,包括FDA批准Dupixent作爲首個用於治療具有嗜酸性表型的COPD的生物治療藥物。從慢性自發性蕁麻疹和水皰性天皰瘡的重要試驗中報告了積極的結果,並計劃進行監管提交。公司的臨牀投資組合擴展到大約40個產品候選。Regeneron保持了強勁的財務狀況,擁有183億美元的現金和可出售證券。公司持續進行股票回購計劃,剩餘29億美元可用。研發投資增長了18%,以支持管道的推進,特別是在晚期腫瘤項目上。
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