Apellis Pharmaceuticals, Inc. (APLS) Q3 2024 Earnings Call Transcript Summary
Apellis Pharmaceuticals, Inc. (APLS) Q3 2024 Earnings Call Transcript Summary
The following is a summary of the Apellis Pharmaceuticals, Inc. (APLS) Q3 2024 Earnings Call Transcript:
以下是Apellis Pharmicals, Inc.(APLS)2024年第三季度業績電話會議記錄摘要:
Financial Performance:
財務業績:
Apellis Pharmaceuticals reported Q3 2024 revenue of approximately $197 million, with SYFOVRE net revenue being $152 million, which more than doubled from the same period last year.
EMPAVELI generated $24.6 million in U.S. product revenue, up 3%.
Net loss was reported at $57.4 million.
SYFOVRE gross to net adjustments impacted revenue, expecting stabilization going forward.
Apellis Pharmicals報告稱,2024年第三季度收入約爲1.97億美元,SYFOVRE淨收入爲1.52億美元,比去年同期翻了一番多。
EMPAVELI在美國創造了2460萬美元的產品收入,增長了3%。
據報道,淨虧損爲5,740萬美元。
SYFOVRE的總淨調整影響了收入,預計未來將保持穩定。
Business Progress:
業務進展:
Apellis has seen continued growth in vial demand for SYFOVRE, claiming approximately 65% market share.
Phase III VALIANT study results for EMPAVELI show potential for it becoming a best-in-class treatment for kidney diseases C3G and IC-MPGN.
Plans for substantial investment in both R&D and commercial activities to support growth.
No plans to pursue EU approval for SYFOVRE.
Apellis對SYFOVRE的瓶裝需求持續增長,佔據了約65%的市場份額。
EMPAVELI的III期VaLiant研究結果表明,它有可能成爲治療腎臟疾病C3G和IC-MPGN的最佳腎臟疾病療法。
計劃對研發和商業活動進行大量投資以支持增長。
沒有計劃尋求歐盟批准SYFOVRE。
Opportunities:
機會:
EMPAVELI has significant potential in rare kidney diseases, building on strong Phase III results.
Plans to leverage robust data from SYFOVRE trials and real-world evidence to strengthen market position.
基於強勁的III期結果,EMPAVELI在罕見腎臟疾病中具有巨大潛力。
計劃利用來自SYFOVRE試驗的可靠數據和真實世界的證據來鞏固市場地位。
Risks:
風險:
Slow uptake in vial growth due to slower market growth dynamics and decision-making pace of retina specialists.
Negative CHMP opinion led to the non-pursuit of EU approval for SYFOVRE.
由於市場增長動態和視網膜專家決策步伐放緩,藥瓶生長吸收緩慢。
CHMP的負面意見導致歐盟不願批准SYFOVRE。
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提示:本文由 AI 生成。無法完全保證內容的準確性。欲了解更多詳情,請訪問投資者關係網站。本文僅供投資者參考,不構成任何投資建議。