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EyePoint Pharmaceuticals | 8-K: Current report

EyePoint Pharmaceuticals | 8-K: Current report

EyePoint Pharmaceuticals | 8-K:重大事件
美股SEC公告 ·  06/26 09:28

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On June 26, 2024, EyePoint Pharmaceuticals, Inc. hosted its R&D Day in New York City, where it presented the 2024 R&D Day Presentation, including estimated cash and investments as of June 30, 2024, and corporate updates. The company also announced clinical and regulatory developments for its lead pipeline program, DURAVYU™ (vorolanib intravitreal insert), based on its Durasert E™ sustained drug delivery technology. The Presentation and a press release were filed with the SEC and included in Exhibits 99.1 and 99.2, respectively. The data presented were preliminary and subject to change pending the completion of the company's quarterly report. EyePoint Pharmaceuticals highlighted the potential of DURAVYU™ as a treatment for serious eye diseases, including wet age-related macular degeneration (AMD), and provided updates on its Phase 2 clinical trial results, which met all primary and secondary endpoints. The company outlined plans for Phase 3 pivotal trials, aiming for FDA approval. The R&D Day also covered the company's early-stage programs and featured discussions with key opinion leaders in ophthalmology.
On June 26, 2024, EyePoint Pharmaceuticals, Inc. hosted its R&D Day in New York City, where it presented the 2024 R&D Day Presentation, including estimated cash and investments as of June 30, 2024, and corporate updates. The company also announced clinical and regulatory developments for its lead pipeline program, DURAVYU™ (vorolanib intravitreal insert), based on its Durasert E™ sustained drug delivery technology. The Presentation and a press release were filed with the SEC and included in Exhibits 99.1 and 99.2, respectively. The data presented were preliminary and subject to change pending the completion of the company's quarterly report. EyePoint Pharmaceuticals highlighted the potential of DURAVYU™ as a treatment for serious eye diseases, including wet age-related macular degeneration (AMD), and provided updates on its Phase 2 clinical trial results, which met all primary and secondary endpoints. The company outlined plans for Phase 3 pivotal trials, aiming for FDA approval. The R&D Day also covered the company's early-stage programs and featured discussions with key opinion leaders in ophthalmology.
2024年6月26日,eyepoint pharmaceuticals公司在紐約舉行了研發日活動,介紹了2024年研發日演示文稿,包括截至2024年6月30日的現金和投資估算以及公司近況更新。此外,該公司還宣佈了基於其Durasert E™緩釋藥物輸送技術的主導產品DURAVYU™(vorolanib眼內植入物)的臨床和監管進展。演示文稿和新聞稿已在SEC提交,幷包含在展示文件99.1和99.2中。所提供的數據爲初步數據,可能隨着公司季報的完成而有所變化。EyePoint Pharmaceuticals凸顯了DURAVYU™在治療嚴重眼部疾病方面的潛力,其中包括溼性年齡相關性黃斑變性,並提供其第二階段臨床試驗結果更新,該試驗達成了所有主要和次要終點。該公司還概述了第三階段關鍵試驗的計劃,旨在獲得FDA批准。研發日還涵蓋了該公司早期項目的特色板塊,並與眼科醫療領域的關鍵意見領袖進行了討論。
2024年6月26日,eyepoint pharmaceuticals公司在紐約舉行了研發日活動,介紹了2024年研發日演示文稿,包括截至2024年6月30日的現金和投資估算以及公司近況更新。此外,該公司還宣佈了基於其Durasert E™緩釋藥物輸送技術的主導產品DURAVYU™(vorolanib眼內植入物)的臨床和監管進展。演示文稿和新聞稿已在SEC提交,幷包含在展示文件99.1和99.2中。所提供的數據爲初步數據,可能隨着公司季報的完成而有所變化。EyePoint Pharmaceuticals凸顯了DURAVYU™在治療嚴重眼部疾病方面的潛力,其中包括溼性年齡相關性黃斑變性,並提供其第二階段臨床試驗結果更新,該試驗達成了所有主要和次要終點。該公司還概述了第三階段關鍵試驗的計劃,旨在獲得FDA批准。研發日還涵蓋了該公司早期項目的特色板塊,並與眼科醫療領域的關鍵意見領袖進行了討論。
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