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:
以下是傳奇生物公司(LEGN)2024年第三季度業績會議記錄摘要:
Financial Performance:
財務業績:
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.
傳奇生物報告,CARVYKTI在2024年第三季度的淨銷售額約爲28600萬美元,同比增長87.6%。
該季度總收入爲16000萬美元。
2024年第三季度淨虧損爲12500萬美元,每股虧損0.34美元。
研發支出同比保持在9600萬美元。
2024年第三季度銷售和分銷費用爲4400萬美元,較去年同期的2100萬美元大幅增加。
Business Progress:
業務進展:
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在二線患者群體中取得了顯著的總生存益處,標誌着多發性骨髓瘤治療邁出了重要的一步。
CARVYKTI已獲得美國FDA和歐洲委員會對二線研究的批准,並獲得中國國家藥品監督管理局對四線及以上研究的批准。
隨着位於比利時Obelisc工廠CARVYKTI生產的批准,生產能力得到了擴展。
Opportunities:
機會:
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.
持續進行全球擴張,特別是在瑞士CARVYKTI獲得批准並進行持續的監管提交。
預計將通過產能增加和新生產設施的批准實現增長。
Risks:
風險:
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.
在競爭激烈的多發性骨髓瘤市場上,成功和CARVYKTI拓展的發展至關重要。
與國際拓展和審批流程相關的監管和市場風險,包括對設施運營和產品研究批准的依賴。
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提示:本文由人工智能生成。內容準確性無法完全保證。如需更全面詳情,請參閱IR網站。本文僅供投資者參考,不具有任何指導或推薦建議。