Legend Biotech Corporation (LEGN) Q3 2024 Earnings Call Transcript Summary
Legend Biotech Corporation (LEGN) Q3 2024 Earnings Call Transcript Summary
The following is a summary of the Legend Biotech Corporation (LEGN) Q3 2024 Earnings Call Transcript:
以下是传奇生物公司(LEGN)2024年第三季度业绩会议记录摘要:
Financial Performance:
财务表现:
Legend Biotech reported Q3 2024 net sales for CARVYKTI were approximately $286 million, representing an 87.6% increase year-over-year.
Total revenues for the quarter were $160 million.
Net loss for Q3 2024 was $125 million or a loss of $0.34 per share.
R&D expenditures remained consistent year-over-year at $96 million.
Selling and distribution expenses for Q3 2024 were $44 million, significantly up from $21 million in the same period last year.
传奇生物报告,CARVYKTI在2024年第三季度的净销售额约为28600万美元,同比增长87.6%。
该季度总收入为16000万美元。
2024年第三季度净亏损为12500万美元,每股亏损0.34美元。
研发支出同比保持在9600万美元。
2024年第三季度销售和分销费用为4400万美元,较去年同期的2100万美元大幅增加。
Business Progress:
业务进展:
CARVYKTI achieved a significant overall survival benefit in second line plus patient population, marking a pivotal milestone in multiple myeloma treatment.
CARVYKTI achieved FDA and European Commission approval for second-line study and received approval from China's National Medical Products Administration for fourth-line plus study.
Expanded production capabilities with the approval of the Obelisc facility in Belgium for CARVYKTI production.
CARVYKTI在二线患者群体中取得了显著的总生存益处,标志着多发性骨髓瘤治疗迈出了重要的一步。
CARVYKTI已获得美国FDA和欧洲委员会对二线研究的批准,并获得中国国家药品监督管理局对四线及以上研究的批准。
随着位于比利时Obelisc工厂CARVYKTI生产的批准,生产能力得到了扩展。
Opportunities:
机会:
Continued global expansion, particularly with the recent approval for CARVYKTI in Switzerland and ongoing regulatory submissions.
Anticipated growth from increased capacity and approval of new production facilities.
持续进行全球扩张,特别是在瑞士CARVYKTI获得批准并进行持续的监管提交。
预计将通过产能增加和新生产设施的批准实现增长。
Risks:
风险:
Dependence on success and expansion of CARVYKTI, especially in competitive multiple myeloma market.
Regulatory and market risks related to international expansion and approval processes, including reliance on approvals for facility operations and product studies.
在竞争激烈的多发性骨髓瘤市场上,成功和CARVYKTI拓展的发展至关重要。
与国际拓展和审批流程相关的监管和市场风险,包括对设施运营和产品研究批准的依赖。
Tips: This article is generated by AI. The accuracy of the content can not be fully guaranteed. For more comprehensive details, please refer to the IR website. The article is only for investors' reference without any guidance or recommendation suggestions.
提示:本文由人工智能生成。内容准确性无法完全保证。如需更全面详情,请参阅IR网站。本文仅供投资者参考,不具有任何指导或推荐建议。