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Avenue Therapeutics | 10-Q: Q3 2024 Earnings Report

Avenue Therapeutics | 10-Q: Q3 2024 Earnings Report

Avenue Therapeutics | 10-Q:2024财年三季报
美股SEC公告 ·  2024/11/15 05:24

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Avenue Therapeutics reported a Q3 2024 net loss of $3.1 million compared to net income of $0.5 million in Q3 2023. Research and development expenses increased to $2.3 million from $0.9 million year-over-year, primarily due to higher pre-clinical and clinical development costs. Cash and cash equivalents stood at $2.6 million as of September 30, 2024.The company made significant progress on its clinical programs, with last patient last visit completed in the Phase 1b/2a trial of AJ201 for SBMA treatment, expecting top-line data around year-end 2024. Additionally, Avenue reached final agreement with FDA on the Phase 3 safety study protocol for IV tramadol, designed to assess opioid-induced respiratory depression risk compared to IV morphine in approximately 300 post-bunionectomy patients.Avenue strengthened its financial position through multiple transactions, including warrant exercises and ATM offerings that generated aggregate net proceeds of $9.1 million during the nine months ended September 30, 2024. However, management indicated current cash is only sufficient to fund operations through first half of 2025 and additional capital will be required to execute the company's development plans.
Avenue Therapeutics reported a Q3 2024 net loss of $3.1 million compared to net income of $0.5 million in Q3 2023. Research and development expenses increased to $2.3 million from $0.9 million year-over-year, primarily due to higher pre-clinical and clinical development costs. Cash and cash equivalents stood at $2.6 million as of September 30, 2024.The company made significant progress on its clinical programs, with last patient last visit completed in the Phase 1b/2a trial of AJ201 for SBMA treatment, expecting top-line data around year-end 2024. Additionally, Avenue reached final agreement with FDA on the Phase 3 safety study protocol for IV tramadol, designed to assess opioid-induced respiratory depression risk compared to IV morphine in approximately 300 post-bunionectomy patients.Avenue strengthened its financial position through multiple transactions, including warrant exercises and ATM offerings that generated aggregate net proceeds of $9.1 million during the nine months ended September 30, 2024. However, management indicated current cash is only sufficient to fund operations through first half of 2025 and additional capital will be required to execute the company's development plans.
Avenue Therapeutics报告显示,2024年第三季度净亏损为310万美元,而2023年第三季度的净利润为50万美元。研发费用同比增加至230万美元,去年的费用为90万美元,主要由于临床前和临床开发成本上升。截至2024年9月30日,现金及现金等价物为260万美元。该公司在其临床项目上取得了重要进展,AJ201在SBMA治疗的1b/2a期试验中完成了最后一位患者的最后一次访问,预计2024年年末将公布顶线数据。此外,Avenue与FDA达成了关于IV曲马多的3期安全性研究协议的最终协议,该协议旨在评估与IV吗啡相比,约300名足趾切除术后患者中阿片类药物导致的呼吸抑制风险。Avenue通过多项交易增强了其财务状况,包括认股权证行使和ATm发行,在截至2024年9月30日的九个月内产生了910万美元的总净收益。然而,管理层表示,目前的现金仅足以支持到2025年上半年,后续进行公司的发展计划还需要额外资金。
Avenue Therapeutics报告显示,2024年第三季度净亏损为310万美元,而2023年第三季度的净利润为50万美元。研发费用同比增加至230万美元,去年的费用为90万美元,主要由于临床前和临床开发成本上升。截至2024年9月30日,现金及现金等价物为260万美元。该公司在其临床项目上取得了重要进展,AJ201在SBMA治疗的1b/2a期试验中完成了最后一位患者的最后一次访问,预计2024年年末将公布顶线数据。此外,Avenue与FDA达成了关于IV曲马多的3期安全性研究协议的最终协议,该协议旨在评估与IV吗啡相比,约300名足趾切除术后患者中阿片类药物导致的呼吸抑制风险。Avenue通过多项交易增强了其财务状况,包括认股权证行使和ATm发行,在截至2024年9月30日的九个月内产生了910万美元的总净收益。然而,管理层表示,目前的现金仅足以支持到2025年上半年,后续进行公司的发展计划还需要额外资金。
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