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Theriva Biologics | 10-Q: Q3 2024 Earnings Report

Theriva Biologics | 10-Q: Q3 2024 Earnings Report

Theriva Biologics | 10-Q:2024財年三季報
美股SEC公告 ·  2024/11/13 00:32

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Theriva Biologics reported a net loss of $7.7 million ($6.81 per share) for Q3 2024, compared to a $3.3 million loss ($4.85 per share) in Q3 2023. Revenue remained minimal while R&D expenses decreased to $2.7 million from $4.0 million year-over-year, primarily due to lower clinical trial costs for the VIRAGE Phase 2 study of VCN-01 in pancreatic cancer. The company recorded impairment charges of $1.3 million for in-process R&D and $1.5 million for goodwill.The company achieved a significant milestone by completing target enrollment of 92 evaluable patients in its VIRAGE Phase 2b trial evaluating VCN-01 plus standard chemotherapy for pancreatic cancer. Thirty patients have received their second doses of VCN-01, which were well tolerated. The company also received EU orphan drug designation for VCN-01 in retinoblastoma treatment.As of September 30, 2024, Theriva had cash and equivalents of $16.4 million, which is expected to fund operations into Q3 2025. The company raised $3.6 million through ATM offerings and $2.0 million through a public offering during the quarter. Management noted substantial doubt about the company's ability to continue as a going concern without additional funding.
Theriva Biologics reported a net loss of $7.7 million ($6.81 per share) for Q3 2024, compared to a $3.3 million loss ($4.85 per share) in Q3 2023. Revenue remained minimal while R&D expenses decreased to $2.7 million from $4.0 million year-over-year, primarily due to lower clinical trial costs for the VIRAGE Phase 2 study of VCN-01 in pancreatic cancer. The company recorded impairment charges of $1.3 million for in-process R&D and $1.5 million for goodwill.The company achieved a significant milestone by completing target enrollment of 92 evaluable patients in its VIRAGE Phase 2b trial evaluating VCN-01 plus standard chemotherapy for pancreatic cancer. Thirty patients have received their second doses of VCN-01, which were well tolerated. The company also received EU orphan drug designation for VCN-01 in retinoblastoma treatment.As of September 30, 2024, Theriva had cash and equivalents of $16.4 million, which is expected to fund operations into Q3 2025. The company raised $3.6 million through ATM offerings and $2.0 million through a public offering during the quarter. Management noted substantial doubt about the company's ability to continue as a going concern without additional funding.
Theriva生物製品報告2024年第三季度淨虧損770萬美元(每股6.81美元),相比2023年第三季度的淨虧損330萬美元(每股4.85美元)。營業收入保持微薄,而研發費用則從去年同期的400萬美元減少至270萬美元,主要是由於在胰腺癌VCN-01的VIRAGE第二階段研究中臨牀試驗費用更低。公司錄得130萬美元的研發中期減值損失和150萬美元的商譽減值。公司通過完成92名可評估患者的靶向入組,在評估VCN-01和標準化療聯合治療胰腺癌的VIRAGE二期試驗中取得了重大里程碑。已有30名患者接受了VCN-01的第二劑量,該劑量耐受性良好。公司還獲得了歐盟孤兒藥物的指定,用於視網膜母細胞瘤的...展開全部
Theriva生物製品報告2024年第三季度淨虧損770萬美元(每股6.81美元),相比2023年第三季度的淨虧損330萬美元(每股4.85美元)。營業收入保持微薄,而研發費用則從去年同期的400萬美元減少至270萬美元,主要是由於在胰腺癌VCN-01的VIRAGE第二階段研究中臨牀試驗費用更低。公司錄得130萬美元的研發中期減值損失和150萬美元的商譽減值。公司通過完成92名可評估患者的靶向入組,在評估VCN-01和標準化療聯合治療胰腺癌的VIRAGE二期試驗中取得了重大里程碑。已有30名患者接受了VCN-01的第二劑量,該劑量耐受性良好。公司還獲得了歐盟孤兒藥物的指定,用於視網膜母細胞瘤的治療。截至2024年9月30日,Theriva擁有現金及現金等價物1640萬美元,預計這將爲其運營提供資金直到2025年第三季度。公司通過ATM增發籌集了360萬美元,並在本季度通過公開發行籌集了200萬美元。管理層表示,公司在沒有額外資金的情況下,存在持續經營能力的重大疑慮。

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