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

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

Chimerix | 8-K:Chimerix公布2024年第二季度财务业绩并提供最新运营情况
美股SEC公告 ·  2024/08/13 04:07

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Chimerix reported a Q2 2024 net loss of $20.7M ($0.23 per share), compared to $18.6M loss in Q2 2023. Research and development expenses increased to $18.4M from $16.9M year-over-year. The company maintained a strong balance sheet with $171.5M in available capital as of June 30, 2024.The Phase 3 ACTION study for dordaviprone in H3 K27M-mutant diffuse glioma remains on track, with first interim overall survival data expected in Q3 2025. The company has filed for Provisional Determination with Australia's Therapeutic Goods Administration, marking the second step toward potential Provisional Approval.ONC206's Phase 1 trials have reached dose level 10 of 11 planned levels, demonstrating dose proportional exposure with no dose-limiting toxicity to date. The company expects to complete enrollment in the remaining dose escalation cohorts by end of 2024, with assessment of objective responses planned for first half of 2025.
Chimerix reported a Q2 2024 net loss of $20.7M ($0.23 per share), compared to $18.6M loss in Q2 2023. Research and development expenses increased to $18.4M from $16.9M year-over-year. The company maintained a strong balance sheet with $171.5M in available capital as of June 30, 2024.The Phase 3 ACTION study for dordaviprone in H3 K27M-mutant diffuse glioma remains on track, with first interim overall survival data expected in Q3 2025. The company has filed for Provisional Determination with Australia's Therapeutic Goods Administration, marking the second step toward potential Provisional Approval.ONC206's Phase 1 trials have reached dose level 10 of 11 planned levels, demonstrating dose proportional exposure with no dose-limiting toxicity to date. The company expects to complete enrollment in the remaining dose escalation cohorts by end of 2024, with assessment of objective responses planned for first half of 2025.
Chimerix报告2024年第二季度净亏损2070万美元(每股0.23美元),相比于2023年第二季度的1860万美元亏损。研发费用同比增加至1840万美元,较上年的1690万美元有所上升。截止到2024年6月30日,该公司保持强劲的资产负债表,拥有可用资本17150万美元。针对dordaviprone的第三阶段ACTION研究在H3 K2700万突变弥漫性胶质瘤中进展顺利,预计在2025年第三季度将获得首次中期整体生存数据。该公司已向澳洲治疗商品管理局提交了临时裁定申请,这标志着潜在临时批准的第二步。ONC206的第一阶段试验已达到计划的11个剂量水平中的第10个剂量水平,显示剂量依赖性暴露,至今未出现剂量限制性毒性。公司预计将在2024年底前完成其余剂量递增队列的入组,计划在2025年上半年进行客观反应评估。
Chimerix报告2024年第二季度净亏损2070万美元(每股0.23美元),相比于2023年第二季度的1860万美元亏损。研发费用同比增加至1840万美元,较上年的1690万美元有所上升。截止到2024年6月30日,该公司保持强劲的资产负债表,拥有可用资本17150万美元。针对dordaviprone的第三阶段ACTION研究在H3 K2700万突变弥漫性胶质瘤中进展顺利,预计在2025年第三季度将获得首次中期整体生存数据。该公司已向澳洲治疗商品管理局提交了临时裁定申请,这标志着潜在临时批准的第二步。ONC206的第一阶段试验已达到计划的11个剂量水平中的第10个剂量水平,显示剂量依赖性暴露,至今未出现剂量限制性毒性。公司预计将在2024年底前完成其余剂量递增队列的入组,计划在2025年上半年进行客观反应评估。
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