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Cybin | 6-K: Report of foreign private issuer (related to financial reporting)

Cybin | 6-K: Report of foreign private issuer (related to financial reporting)

Cybin | 6-K:外国发行人报告(业绩相关)
美股SEC公告 ·  2024/08/08 11:44

Moomoo AI 已提取核心信息

Cybin Inc. reported a net loss of $14.8M for Q1 fiscal 2025 ended June 30, 2024, compared to $14.5M in the prior year period. Operating expenses increased to $20.3M from $12.7M, primarily due to expanded research programs and higher share-based compensation.Research expenses rose to $8.0M from $6.4M as the company advanced clinical trials of CYB003 for major depressive disorder and CYB004 for anxiety disorders. General and administrative costs increased to $8.3M from $5.0M due to higher capital market and investor relations spending. The company maintained a strong cash position of $183.3M as of June 30, 2024.Key operational highlights included receiving FDA Breakthrough Therapy Designation for CYB003, showing positive 4-month durability data in Phase 2a MDD study, and initiating a Phase 2 study of CYB004 in generalized anxiety disorder. The company plans to begin Phase 3 trials of CYB003 in late summer 2024 and expects topline Phase 2 GAD data for CYB004 by early 2025.
Cybin Inc. reported a net loss of $14.8M for Q1 fiscal 2025 ended June 30, 2024, compared to $14.5M in the prior year period. Operating expenses increased to $20.3M from $12.7M, primarily due to expanded research programs and higher share-based compensation.Research expenses rose to $8.0M from $6.4M as the company advanced clinical trials of CYB003 for major depressive disorder and CYB004 for anxiety disorders. General and administrative costs increased to $8.3M from $5.0M due to higher capital market and investor relations spending. The company maintained a strong cash position of $183.3M as of June 30, 2024.Key operational highlights included receiving FDA Breakthrough Therapy Designation for CYB003, showing positive 4-month durability data in Phase 2a MDD study, and initiating a Phase 2 study of CYB004 in generalized anxiety disorder. The company plans to begin Phase 3 trials of CYB003 in late summer 2024 and expects topline Phase 2 GAD data for CYB004 by early 2025.
Cybin Inc. 报告了截至2024年6月30日的2025财年第一季度净亏损为1480万美元,相较于去年同期的1450万美元。营业费用从1270万美元增加至2030万美元,主要由于研究项目扩大和较高的分享基础补偿所致。研究费用从640万美元上升至800万美元,因为公司推进了CYB003用于重度抑郁症和CYB004用于焦虑症的临床试验。由于资本市场和投资者关系支出增加,一般和行政费用从500万美元增加至830万美元。截止2024年6月30日,公司保持了18330万美元的强劲现金头寸。关键运营亮点包括获得FDA的CYB003突破性疗法标志,显示在2a期MDD研究中的4个月阳性耐久性数据,并启动了CYB004在广泛性焦虑症中的2期研究。公司计划在2024年夏末开始CYB003的3期试验,并预计在2025年初获得CYB004的2期广泛性焦虑症数据。
Cybin Inc. 报告了截至2024年6月30日的2025财年第一季度净亏损为1480万美元,相较于去年同期的1450万美元。营业费用从1270万美元增加至2030万美元,主要由于研究项目扩大和较高的分享基础补偿所致。研究费用从640万美元上升至800万美元,因为公司推进了CYB003用于重度抑郁症和CYB004用于焦虑症的临床试验。由于资本市场和投资者关系支出增加,一般和行政费用从500万美元增加至830万美元。截止2024年6月30日,公司保持了18330万美元的强劲现金头寸。关键运营亮点包括获得FDA的CYB003突破性疗法标志,显示在2a期MDD研究中的4个月阳性耐久性数据,并启动了CYB004在广泛性焦虑症中的2期研究。公司计划在2024年夏末开始CYB003的3期试验,并预计在2025年初获得CYB004的2期广泛性焦虑症数据。
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