share_log

Invivyd | 10-Q: Q2 2024 Earnings Report

Invivyd | 10-Q: Q2 2024 Earnings Report

Invivyd | 10-Q:2024财年二季报
美股SEC公告 ·  08/14 08:29

Moomoo AI 已提取核心信息

Invivyd, a biopharmaceutical company, reported financial results and business developments for the quarter ended June 30, 2024. The company generated $2.3 million in product revenue, net, following the launch of PEMGARDA, its monoclonal antibody for COVID-19. Research and development expenses decreased by $13.3 million to $30.3 million compared to the same period in 2023, primarily due to reduced costs associated with the VYD222 program, partially offset by increased costs for the VYD2311 program. Selling, general, and administrative expenses increased by $11.0 million to $21.1 million, reflecting the commercialization of PEMGARDA. Invivyd's net loss for the quarter was $47.2 million, a slight improvement from the $50.2 million loss in the previous year. The company's cash and cash equivalents stood at $147.9 million as of June 30, 2024. Invivyd's INVYMAB platform is designed to...Show More
Invivyd, a biopharmaceutical company, reported financial results and business developments for the quarter ended June 30, 2024. The company generated $2.3 million in product revenue, net, following the launch of PEMGARDA, its monoclonal antibody for COVID-19. Research and development expenses decreased by $13.3 million to $30.3 million compared to the same period in 2023, primarily due to reduced costs associated with the VYD222 program, partially offset by increased costs for the VYD2311 program. Selling, general, and administrative expenses increased by $11.0 million to $21.1 million, reflecting the commercialization of PEMGARDA. Invivyd's net loss for the quarter was $47.2 million, a slight improvement from the $50.2 million loss in the previous year. The company's cash and cash equivalents stood at $147.9 million as of June 30, 2024. Invivyd's INVYMAB platform is designed to rapidly generate new monoclonal antibodies to keep pace with evolving viral threats. The company received emergency use authorization (EUA) from the FDA for PEMGARDA in March 2024 and submitted a request to amend the EUA for treatment of mild-to-moderate symptomatic COVID-19 in certain immunocompromised patients in July 2024. Invivyd plans to leverage its platform to introduce new or engineered monoclonal antibody candidates periodically and to apply the platform to other viral diseases such as influenza.
生物制药公司Invivyd报道了截至2024年6月30日季度财务业绩和业务发展。该公司推出了其针对COVID-19的单克隆抗体PEMGARDA后,产品营业收入净额为230万美元。与2023年同期相比,研发费用减少了1330万美元,至3030万美元,主要由于VYD222项目相关成本降低,部分抵消了VYD2311项目成本的增加。销售、普通和管理费用增加了1100万美元,至2110万美元,反映出PEMGARDA的商业化。Invivyd本季净亏损为4720万美元,略好于前一年的5020万美元亏损。截至2024年6月30日,公司现金及现金等价物为14790万美元。Invivyd的INVYMAb平台旨在快...展开全部
生物制药公司Invivyd报道了截至2024年6月30日季度财务业绩和业务发展。该公司推出了其针对COVID-19的单克隆抗体PEMGARDA后,产品营业收入净额为230万美元。与2023年同期相比,研发费用减少了1330万美元,至3030万美元,主要由于VYD222项目相关成本降低,部分抵消了VYD2311项目成本的增加。销售、普通和管理费用增加了1100万美元,至2110万美元,反映出PEMGARDA的商业化。Invivyd本季净亏损为4720万美元,略好于前一年的5020万美元亏损。截至2024年6月30日,公司现金及现金等价物为14790万美元。Invivyd的INVYMAb平台旨在快速生成新的单克隆抗体,以跟上病毒威胁的发展。该公司于2024年3月获得了FDA的紧急使用授权(EUA)用于PEMGARDA,并于2024年7月提交了一份修改EUA的请求,用于治疗某些免疫受损患者的轻至中度症状COVID-19。Invivyd计划利用其平台定期引入新的或改良的单克隆抗体候选者,并将该平台应用于其他病毒性疾病,如流感。
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