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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:外國發行人報告(業績相關)
美股SEC公告 ·  2024/08/09 01:44

Moomoo AI 已提取核心訊息

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. 在截至2024年6月30日的2025財年第一季度報告了1480萬美元的淨虧損,而上年同期爲1450萬美元。營業費用從1270萬美元增加到2030萬美元,主要由於研究項目的擴大和更高的分享基礎補償。由於公司推進了針對重度抑鬱症的CYB003和針對焦慮症的CYB004的臨牀試驗,研究費用從640萬美元上升至800萬美元。由於資本市場和投資者關係支出的增加,一般和行政成本從500萬美元增加到830萬美元。截至2024年6月30日,公司保持了18330萬美元的強勁現金頭寸。主要運營亮點包括獲得FDA對CYB003的突破性療法認定,在2a期重度抑鬱症研究中顯示出正面的4個月耐用性數據,並啓動了對廣泛性焦慮症的CYB004的2期研究。公司計劃在2024年夏末開始CYB003的3期試驗,並預計在2025年初獲得CYB004的2期廣泛性焦慮症的高管數據。
Cybin Inc. 在截至2024年6月30日的2025財年第一季度報告了1480萬美元的淨虧損,而上年同期爲1450萬美元。營業費用從1270萬美元增加到2030萬美元,主要由於研究項目的擴大和更高的分享基礎補償。由於公司推進了針對重度抑鬱症的CYB003和針對焦慮症的CYB004的臨牀試驗,研究費用從640萬美元上升至800萬美元。由於資本市場和投資者關係支出的增加,一般和行政成本從500萬美元增加到830萬美元。截至2024年6月30日,公司保持了18330萬美元的強勁現金頭寸。主要運營亮點包括獲得FDA對CYB003的突破性療法認定,在2a期重度抑鬱症研究中顯示出正面的4個月耐用性數據,並啓動了對廣泛性焦慮症的CYB004的2期研究。公司計劃在2024年夏末開始CYB003的3期試驗,並預計在2025年初獲得CYB004的2期廣泛性焦慮症的高管數據。
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