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

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

Compugen醫療 | 6-K:外國發行人報告(業績相關)
美股SEC公告 ·  2024/08/06 19:03

牛牛AI助理已提取核心訊息

Compugen reported Q2 2024 financial results, highlighting FDA clearance of COM503 IND which triggered a $30 million milestone payment from Gilead. The company recorded revenues of $6.7 million and reduced net loss to $2.1 million compared to $9.3 million in Q2 2023. Cash position stood at $92.3 million as of June 30, 2024, expected to fund operations into 2027.The company remains on track to present data from COM701 + COM902 + pembrolizumab study in platinum resistant ovarian cancer in Q4 2024. Previous data showed encouraging results with 20% overall response rate and durable responses lasting over 16 months. Additionally, partner AstraZeneca is advancing rilvegostomig development with a projected non-risk-adjusted peak year revenue target exceeding $5 billion.R&D expenses decreased to $6.2 million from $7.8 million year-over-year, while G&A expenses slightly reduced to $2.2 million. The company plans to initiate a Phase 1 trial for COM503 as monotherapy and in combination with zimberelimab in advanced solid tumors in Q4 2024.
Compugen reported Q2 2024 financial results, highlighting FDA clearance of COM503 IND which triggered a $30 million milestone payment from Gilead. The company recorded revenues of $6.7 million and reduced net loss to $2.1 million compared to $9.3 million in Q2 2023. Cash position stood at $92.3 million as of June 30, 2024, expected to fund operations into 2027.The company remains on track to present data from COM701 + COM902 + pembrolizumab study in platinum resistant ovarian cancer in Q4 2024. Previous data showed encouraging results with 20% overall response rate and durable responses lasting over 16 months. Additionally, partner AstraZeneca is advancing rilvegostomig development with a projected non-risk-adjusted peak year revenue target exceeding $5 billion.R&D expenses decreased to $6.2 million from $7.8 million year-over-year, while G&A expenses slightly reduced to $2.2 million. The company plans to initiate a Phase 1 trial for COM503 as monotherapy and in combination with zimberelimab in advanced solid tumors in Q4 2024.
Compugen醫療公佈了2024年第二季度財務業績,強調了COM503 IND獲得FDA批准,這觸發了來自吉利德的3000萬美元里程碑付款。該公司報告營業收入爲670萬美元,淨虧損減少至210萬美元,相較於2023年第二季度的930萬美元。截止到2024年6月30日,現金狀況爲9230萬美元,預計將支持其運營直到2027年。該公司仍按計劃在2024年第四季度展示關於COM701 + COM902 + Pembrolizumab研究在鉑金耐藥卵巢癌中的數據。之前的數據表明,整體應答率爲20%,並且持久反應持續超過16個月。此外,合作伙伴阿斯利康正在推進rilvegostomig的開發,預計非風險調整的峯值年度營業收入目標超過50億元。研發費用同比減少至620萬美元,去年爲780萬美元,而一般管理費用略微減少至220萬美元。該公司計劃於2024年第四季度啓動COM503的單藥和與zimberelimab聯合用於晚期實體瘤的第一階段試驗。
Compugen醫療公佈了2024年第二季度財務業績,強調了COM503 IND獲得FDA批准,這觸發了來自吉利德的3000萬美元里程碑付款。該公司報告營業收入爲670萬美元,淨虧損減少至210萬美元,相較於2023年第二季度的930萬美元。截止到2024年6月30日,現金狀況爲9230萬美元,預計將支持其運營直到2027年。該公司仍按計劃在2024年第四季度展示關於COM701 + COM902 + Pembrolizumab研究在鉑金耐藥卵巢癌中的數據。之前的數據表明,整體應答率爲20%,並且持久反應持續超過16個月。此外,合作伙伴阿斯利康正在推進rilvegostomig的開發,預計非風險調整的峯值年度營業收入目標超過50億元。研發費用同比減少至620萬美元,去年爲780萬美元,而一般管理費用略微減少至220萬美元。該公司計劃於2024年第四季度啓動COM503的單藥和與zimberelimab聯合用於晚期實體瘤的第一階段試驗。

譯文內容由第三人軟體翻譯。


牛牛AI助手部分由第三方人工智慧模型基於資訊內容自動產生。


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