share_log

Theriva Biologics | 10-Q: Q3 2024 Earnings Report

Theriva Biologics | 10-Q: Q3 2024 Earnings Report

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

Moomoo AI 已提取核心信息

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生物制品报告2024年第三季度净亏损770万美元(每股6.81美元),相比2023年第三季度的净亏损330万美元(每股4.85美元)。营业收入保持微薄,而研发费用则从去年同期的400万美元减少至270万美元,主要是由于在胰腺癌VCN-01的VIRAGE第二阶段研究中临床试验费用更低。公司录得130万美元的研发中期减值损失和150万美元的商誉减值。公司通过完成92名可评估患者的靶向入组,在评估VCN-01和标准化疗联合治疗胰腺癌的VIRAGE二期试验中取得了重大里程碑。已有30名患者接受了VCN-01的第二剂量,该剂量耐受性良好。公司还获得了欧盟孤儿药物的指定,用于视网膜母细胞瘤的...展开全部
Theriva生物制品报告2024年第三季度净亏损770万美元(每股6.81美元),相比2023年第三季度的净亏损330万美元(每股4.85美元)。营业收入保持微薄,而研发费用则从去年同期的400万美元减少至270万美元,主要是由于在胰腺癌VCN-01的VIRAGE第二阶段研究中临床试验费用更低。公司录得130万美元的研发中期减值损失和150万美元的商誉减值。公司通过完成92名可评估患者的靶向入组,在评估VCN-01和标准化疗联合治疗胰腺癌的VIRAGE二期试验中取得了重大里程碑。已有30名患者接受了VCN-01的第二剂量,该剂量耐受性良好。公司还获得了欧盟孤儿药物的指定,用于视网膜母细胞瘤的治疗。截至2024年9月30日,Theriva拥有现金及现金等价物1640万美元,预计这将为其运营提供资金直到2025年第三季度。公司通过ATM增发筹集了360万美元,并在本季度通过公开发行筹集了200万美元。管理层表示,公司在没有额外资金的情况下,存在持续经营能力的重大疑虑。
声明:本内容仅用作提供资讯及教育之目的,不构成对任何特定投资或投资策略的推荐或认可。 更多信息