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Chimerix | 10-Q: Q3 2024 Earnings Report

Chimerix | 10-Q: Q3 2024 Earnings Report

Chimerix | 10-Q:2024财年三季报
美股SEC公告 ·  2024/11/07 20:33

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Chimerix reported Q3 2024 revenues of $26,000 and a net loss of $22.9 million ($0.26 per share), compared to revenues of $11,000 and a net loss of $24.0 million ($0.27 per share) in Q3 2023. Research and development expenses increased to $19.6 million from $17.4 million YoY, primarily due to costs related to the Phase 3 ACTION study of dordaviprone and manufacturing expenses.The company continues to advance its Phase 3 ACTION trial evaluating dordaviprone for H3 K27M-mutant diffuse glioma, with over 145 sites now enrolling patients across 15 countries. A recent Independent Data Monitoring Committee safety review recommended the study continue as planned. Management expects interim overall survival data to be available in Q3 2025.As of September 30, 2024, Chimerix maintained a strong financial position with $152.4 million in capital available to fund operations. The company is also pursuing potential approval pathways in Australia, having received Provisional Determination approval in August 2024 and Orphan Drug Designation in September 2024. The company continues development of second-generation compound ONC206, with dose escalation studies expected to complete in 2024.
Chimerix reported Q3 2024 revenues of $26,000 and a net loss of $22.9 million ($0.26 per share), compared to revenues of $11,000 and a net loss of $24.0 million ($0.27 per share) in Q3 2023. Research and development expenses increased to $19.6 million from $17.4 million YoY, primarily due to costs related to the Phase 3 ACTION study of dordaviprone and manufacturing expenses.The company continues to advance its Phase 3 ACTION trial evaluating dordaviprone for H3 K27M-mutant diffuse glioma, with over 145 sites now enrolling patients across 15 countries. A recent Independent Data Monitoring Committee safety review recommended the study continue as planned. Management expects interim overall survival data to be available in Q3 2025.As of September 30, 2024, Chimerix maintained a strong financial position with $152.4 million in capital available to fund operations. The company is also pursuing potential approval pathways in Australia, having received Provisional Determination approval in August 2024 and Orphan Drug Designation in September 2024. The company continues development of second-generation compound ONC206, with dose escalation studies expected to complete in 2024.
Chimerix公布2024年第三季度收入为26000美元,净亏损为2290万 ($0.26每股),相比之下,2023年第三季度收入为11000美元,净亏损为2400万 ($0.27每股)。研发支出同比增加至1960万,去年为1740万,主要是由于与dordaviprone的第三阶段ACTION研究及制造业-半导体费用相关。该公司继续推进评估dordaviprone用于H3 K2700万.mutant弥漫性胶质瘤的第三阶段ACTION试验,现已有超过145个地点在15个国家招募患者。最近,独立数据监测委员会的安全审查建议继续按计划进行该研究。管理层预计在2025年第三季度将提供中期总体生存数据...展开全部
Chimerix公布2024年第三季度收入为26000美元,净亏损为2290万 ($0.26每股),相比之下,2023年第三季度收入为11000美元,净亏损为2400万 ($0.27每股)。研发支出同比增加至1960万,去年为1740万,主要是由于与dordaviprone的第三阶段ACTION研究及制造业-半导体费用相关。该公司继续推进评估dordaviprone用于H3 K2700万.mutant弥漫性胶质瘤的第三阶段ACTION试验,现已有超过145个地点在15个国家招募患者。最近,独立数据监测委员会的安全审查建议继续按计划进行该研究。管理层预计在2025年第三季度将提供中期总体生存数据。截至2024年9月30日,Chimerix保持强劲的财务状况,拥有15240万的资金可用于运营。该公司还在澳洲寻求潜在的批准途径,于2024年8月获得暂时决定批准,并于2024年9月获得孤儿药认定。该公司继续开发第二代Compound ONC206,预计在2024年完成剂量递增研究。
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