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Chimerix | 8-K: Chimerix Reports Third Quarter 2024 Financial Results and Provides Operational Update

Chimerix | 8-K: Chimerix Reports Third Quarter 2024 Financial Results and Provides Operational Update

Chimerix | 8-K:Chimerix公布2024年第三季度财务业绩并提供最新运营情况
美股SEC公告 ·  2024/11/07 06:13

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Chimerix reported a Q3 2024 net loss of $22.9M ($0.26 per share), compared to $24.0M loss in Q3 2023. Research and development expenses increased to $19.6M from $17.4M, while general and administrative expenses decreased to $5.2M from $9.3M. The company maintained a strong balance sheet with $152.4M in available capital as of September 30, 2024.The Phase 3 ACTION study for dordaviprone in H3 K27M-mutant diffuse glioma continues to progress, with first interim overall survival data expected in Q3 2025. The Independent Data Monitoring Committee recommended continuing the study as planned following a safety review. Additionally, Chimerix received alignment from Australia's TGA for Provisional Approval submission, with potential commercial availability by year-end 2025.The company promoted Dr. Josh Allen to Chief Scientific Officer and continues dose escalation studies of ONC206, with enrollment completion expected in 2024. ONC206 has shown no dose-limiting toxicity across 80+ patients, with objective response assessment planned for H1 2025.
Chimerix reported a Q3 2024 net loss of $22.9M ($0.26 per share), compared to $24.0M loss in Q3 2023. Research and development expenses increased to $19.6M from $17.4M, while general and administrative expenses decreased to $5.2M from $9.3M. The company maintained a strong balance sheet with $152.4M in available capital as of September 30, 2024.The Phase 3 ACTION study for dordaviprone in H3 K27M-mutant diffuse glioma continues to progress, with first interim overall survival data expected in Q3 2025. The Independent Data Monitoring Committee recommended continuing the study as planned following a safety review. Additionally, Chimerix received alignment from Australia's TGA for Provisional Approval submission, with potential commercial availability by year-end 2025.The company promoted Dr. Josh Allen to Chief Scientific Officer and continues dose escalation studies of ONC206, with enrollment completion expected in 2024. ONC206 has shown no dose-limiting toxicity across 80+ patients, with objective response assessment planned for H1 2025.
Chimerix报告2024年第三季度净亏损2290万美元(每股$0.26),相比之下,2023年第三季度亏损2400万美元。研究和开发费用增加至1960万美元,从1740万美元上升,而一般和管理费用减少至520万美元,从930万美元下降。截止2024年9月30日,公司保持了强健的资产负债表,拥有15240万美元可用资本。用于dordaviprone在H3 K2700万突变弥漫性胶质瘤的第三阶段ACTION研究继续推进,预计2025年第三季度将公布第一阶段总体生存数据。独立数据监测委员会在安全审查后建议按照计划继续进行研究。此外,Chimerix已获得澳洲TGA的临时批准提交的一致意见,预计到2025年底可能会有商业可用性。公司提拔Dr. Josh Allen为首席科学官,并继续进行ONC206的剂量递增研究,预计在2024年完成招募。ONC206在80多名患者中未显示剂量限制的毒性,计划在2025年上半年进行客观反应评估。
Chimerix报告2024年第三季度净亏损2290万美元(每股$0.26),相比之下,2023年第三季度亏损2400万美元。研究和开发费用增加至1960万美元,从1740万美元上升,而一般和管理费用减少至520万美元,从930万美元下降。截止2024年9月30日,公司保持了强健的资产负债表,拥有15240万美元可用资本。用于dordaviprone在H3 K2700万突变弥漫性胶质瘤的第三阶段ACTION研究继续推进,预计2025年第三季度将公布第一阶段总体生存数据。独立数据监测委员会在安全审查后建议按照计划继续进行研究。此外,Chimerix已获得澳洲TGA的临时批准提交的一致意见,预计到2025年底可能会有商业可用性。公司提拔Dr. Josh Allen为首席科学官,并继续进行ONC206的剂量递增研究,预计在2024年完成招募。ONC206在80多名患者中未显示剂量限制的毒性,计划在2025年上半年进行客观反应评估。
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