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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公佈2024年第二季度財務業績並提供最新運營情況
美股SEC公告 ·  2024/08/13 19:07

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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報告2024年第二季度淨虧損2070萬美元(每股0.23美元),相比2023年第二季度的1860萬美元虧損,虧損有所增加。研發費用同比增長至1840萬美元,高於去年的1690萬美元。截止2024年6月30日,公司保持強勁的資產負債表,擁有可用資本17150萬美元。第三階段ACTION研究正在進行中,針對H3 K2700萬.mutant擴散性膠質瘤的dordaviprone,預計在2025年第三季度發佈首次中期整體生存數據。公司已向澳洲藥品管理局提交臨時裁定申請,這是獲得潛在臨時批准的第二步。ONC206的第一階段試驗已達成11個計劃水平中的第10個劑量水平,顯示出劑量相稱的暴露,迄今未出現劑量限制性毒性。公司預計將在2024年底前完成剩餘劑量遞增隊列的入組,並計劃在2025年上半年評估客觀反應。
Chimerix報告2024年第二季度淨虧損2070萬美元(每股0.23美元),相比2023年第二季度的1860萬美元虧損,虧損有所增加。研發費用同比增長至1840萬美元,高於去年的1690萬美元。截止2024年6月30日,公司保持強勁的資產負債表,擁有可用資本17150萬美元。第三階段ACTION研究正在進行中,針對H3 K2700萬.mutant擴散性膠質瘤的dordaviprone,預計在2025年第三季度發佈首次中期整體生存數據。公司已向澳洲藥品管理局提交臨時裁定申請,這是獲得潛在臨時批准的第二步。ONC206的第一階段試驗已達成11個計劃水平中的第10個劑量水平,顯示出劑量相稱的暴露,迄今未出現劑量限制性毒性。公司預計將在2024年底前完成剩餘劑量遞增隊列的入組,並計劃在2025年上半年評估客觀反應。
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