Altimmune, Inc. (ALT) Q3 2024 Earnings Call Transcript Summary
Altimmune, Inc. (ALT) Q3 2024 Earnings Call Transcript Summary
The following is a summary of the Altimmune, Inc. (ALT) Q3 2024 Earnings Call Transcript:
以下是altimmune公司(ALT)2024年第三季度業績會簡報:
Financial Performance:
財務表現:
Altimmune ended Q3 2024 with $139.4 million in cash, cash equivalents, and short-term investments.
Research and development expenses were $19.8 million for the quarter.
General and administrative expenses were $5 million, reflecting a slight increase due to a rise in professional services costs.
Net loss for the quarter was $22.8 million, translating to a net loss per share of $0.32.
Altimmune在2024年第三季度以13940萬美元的現金、現金等價物和短期投資結束。
本季度研發費用爲1980萬美元。
一般和行政費用爲500萬美元,反映出由於專業服務成本上升略有增加。
本季度淨虧損爲2280萬美元,每股淨虧損爲0.32美元。
Business Progress:
業務進展:
Phase 2b IMPACT trial of pemvidutide in MASH is fully enrolled with top-line efficacy data expected in Q2 2025.
Completed alignment with the FDA for a comprehensive Phase 3 registration program for pemvidutide in obesity.
Plans to submit an IND by end of 2024 and initiate a Phase 2 trial in H1 2025 for additional indications leveraging pemvidutide's attributes.
Entered into a strategic partnership centered on obesity, with preparations to initiate a Phase 3 program in MASH by the end of next year.
Phase 20億IMPACt試驗中MASH中pemvidutide的研究已完全招募滿員,預計2025年第二季度公佈首要療效數據。
與FDA完成了關於pemvidutide在肥胖症的全面三期註冊計劃的對齊。
計劃在2024年底提交IND,並在2025年上半年開始一項第2階段試驗,以利用pemvidutide的屬性進行額外適應症的研究。
簽署了一項以肥胖症爲中心的戰略合作伙伴關係,準備在明年年底前啓動關於MASH的三期計劃。
Opportunities:
機會:
Pemvidutide's potential in both obesity and MASH treatments, given its distinctive dual action as a GLP-1-glucagon receptor agonist.
Expansion into additional indications for pemvidutide, which could significantly broaden its market and therapeutic impact.
Pursuing strategic partnerships centered around obesity to enhance development and commercialization efforts.
鑑於pemvidutide作爲GLP-1-胰高血糖素受體激動劑具有獨特的雙重作用,因此在肥胖症和MASH治療中具有潛力。
擴大pemvidutide的額外適應症範圍,這可能會顯著擴大其市場和治療影響。
尋求以肥胖症爲中心的戰略合作伙伴關係,以增強開發和商業化工作的努力。
Risks:
風險:
No explicit risks mentioned directly, however, the company's advancing clinical trials and extensive R&D investments imply inherent risk in clinical success and regulatory approval.
未直接提及明確風險,但公司不斷推進的臨床試驗和大量的研發投資意味着在臨床成功和監管批准方面存在潛在風險。
Tips: 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:如需更全面的詳情,請參閱投資人關係網站。本文僅供投資者參考,不作任何指引或建議。
譯文內容由第三人軟體翻譯。