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EyePoint Pharmaceuticals | 8-K: EyePoint Pharmaceuticals Reports Second Quarter 2024 Financial Results and Highlights Recent Corporate Developments

EyePoint Pharmaceuticals | 8-K: EyePoint Pharmaceuticals Reports Second Quarter 2024 Financial Results and Highlights Recent Corporate Developments

EyePoint Pharmaceuticals | 8-K:EyePoint Pharmicals公佈2024年第二季度財務業績並重點介紹最近的公司發展
美股SEC公告 ·  2024/08/07 19:01

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EyePoint Pharmaceuticals reported Q2 2024 financial results with total revenue of $9.5 million, including $8.4 million from royalties and collaborations. The company ended the quarter with $280.2 million in cash and investments, providing runway through Phase 3 wet AMD topline data in 2026. Net loss was $30.8 million, or $0.58 per share.The company's lead candidate DURAVYU demonstrated positive 12-month data from Phase 2 DAVIO 2 trial in wet AMD, showing statistically non-inferior visual acuity maintenance compared to aflibercept control. Approximately 50% of DURAVYU-treated patients remained supplement-free after a single injection, with no drug-related serious adverse events reported.EyePoint is advancing its Phase 3 LUGANO pivotal trial for DURAVYU in wet AMD, with over 110 sites committed and first patient dosing expected in 2024. The Phase 2 VERONA trial in diabetic macular edema is fully enrolled with topline data anticipated in Q1 2025. The company completed a positive End of Phase 2 FDA meeting, aligning on the pathway to potential approval.
EyePoint Pharmaceuticals reported Q2 2024 financial results with total revenue of $9.5 million, including $8.4 million from royalties and collaborations. The company ended the quarter with $280.2 million in cash and investments, providing runway through Phase 3 wet AMD topline data in 2026. Net loss was $30.8 million, or $0.58 per share.The company's lead candidate DURAVYU demonstrated positive 12-month data from Phase 2 DAVIO 2 trial in wet AMD, showing statistically non-inferior visual acuity maintenance compared to aflibercept control. Approximately 50% of DURAVYU-treated patients remained supplement-free after a single injection, with no drug-related serious adverse events reported.EyePoint is advancing its Phase 3 LUGANO pivotal trial for DURAVYU in wet AMD, with over 110 sites committed and first patient dosing expected in 2024. The Phase 2 VERONA trial in diabetic macular edema is fully enrolled with topline data anticipated in Q1 2025. The company completed a positive End of Phase 2 FDA meeting, aligning on the pathway to potential approval.
EyePoint Pharmaceuticals報告了2024年第二季度的財務結果,總營業收入爲950萬美元,其中包括來自特許權使用費和合作的840萬美元。該公司在季度末現金和投資總額爲28020萬美元,爲2026年溼性年齡相關性黃斑變性(wet AMD)第三階段的頂線數據提供了資金保障。淨虧損爲3080萬美元,或每股0.58美元。公司的主導候選藥物DURAVYU在溼性年齡相關性黃斑變性(wet AMD)的第二階段DAVIO 2試驗中展示了積極的12個月數據,顯示與阿柏西普對照組相比,視覺敏銳度的維持具有統計學上的非劣效性。約50%的DURAVYU接受治療的患者在單次注射後繼續無補充治療,未報...展開全部
EyePoint Pharmaceuticals報告了2024年第二季度的財務結果,總營業收入爲950萬美元,其中包括來自特許權使用費和合作的840萬美元。該公司在季度末現金和投資總額爲28020萬美元,爲2026年溼性年齡相關性黃斑變性(wet AMD)第三階段的頂線數據提供了資金保障。淨虧損爲3080萬美元,或每股0.58美元。公司的主導候選藥物DURAVYU在溼性年齡相關性黃斑變性(wet AMD)的第二階段DAVIO 2試驗中展示了積極的12個月數據,顯示與阿柏西普對照組相比,視覺敏銳度的維持具有統計學上的非劣效性。約50%的DURAVYU接受治療的患者在單次注射後繼續無補充治療,未報告與藥物相關的嚴重不良事件。EyePoint正在推進其DURAVYU在溼性年齡相關性黃斑變性(wet AMD)中的第三階段LUGANO關鍵試驗,已承諾超過110個站點,預計在2024年開始首次患者給藥。針對糖尿病性黃斑水腫的第二階段VERONA試驗已完全招募,預計在2025年第一季度公佈頂線數據。該公司完成了一次積極的第二階段結束FDA會議,達成潛在批准的路徑一致。
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