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6-K: Report of foreign private issuer [Rules 13a-16 and 15d-16]

6-K: Report of foreign private issuer [Rules 13a-16 and 15d-16]

6-K:外國發行人報告
美股SEC公告 ·  10/30 21:46

牛牛AI助理已提取核心訊息

NeuroSense Therapeutics Ltd., a foreign private issuer, has announced the completion of its 18-month dosing schedule for the PARADIGM Phase 2b ALS clinical trial as of October 2024. The company has reached a significant milestone with the Last Patient Last Visit and is preparing to report the top-line clinical results from the full study in early December 2024. This information was disclosed in their Report on Form 6-K filed with the United States Securities and Exchange Commission (SEC). The report is also incorporated by reference into the company's existing Registration Statements on Form S-8 and Form F-3. NeuroSense Therapeutics has cautioned that the report contains forward-looking statements which are subject to risks and uncertainties, and actual results may differ materially...Show More
NeuroSense Therapeutics Ltd., a foreign private issuer, has announced the completion of its 18-month dosing schedule for the PARADIGM Phase 2b ALS clinical trial as of October 2024. The company has reached a significant milestone with the Last Patient Last Visit and is preparing to report the top-line clinical results from the full study in early December 2024. This information was disclosed in their Report on Form 6-K filed with the United States Securities and Exchange Commission (SEC). The report is also incorporated by reference into the company's existing Registration Statements on Form S-8 and Form F-3. NeuroSense Therapeutics has cautioned that the report contains forward-looking statements which are subject to risks and uncertainties, and actual results may differ materially from those anticipated. These statements include anticipated timelines for reporting clinical trial results and discussions with regulatory authorities such as the FDA and Health Canada. The company has outlined potential risks in its filings, including delays in reporting results, unexpected R&D costs, and the efficacy and safety of their product candidate, PrimeC. The company's latest Annual Report on Form 20-F filed with the SEC on April 4, 2024, contains a detailed discussion of these risk factors.
神經感知生物技術有限公司(NeuroSense Therapeutics Ltd.)作爲一家外國私人發行人,宣佈截至2024年10月,已完成其爲期18個月的PARADIGm第20億ALS臨床試驗的給藥計劃。公司已達到最後受試者最後訪視的重要里程碑,正準備在2024年12月初公佈全面研究的頭條臨床結果。這些信息已在其提交給美國證券交易委員會(SEC)的6-k表格中披露。該報告還被作爲參考併入公司現有的S-8和F-3表格的註冊聲明中。神經感知生物技術已警告稱,該報告包含前瞻性聲明,可能受到風險和不確定性的影響,實際結果可能與預期有所不同。這些聲明包括報告臨床試驗結果的預期時間表,以及與FDA和加拿大衛生部等監管機構的討論。公司在其備案中概述了潛在的風險,包括延遲報告結果、意外研發成本和其產品候選者PrimeC的功效和安全性。公司在2024年4月4日向SEC提交的最新20-F年度報告詳細討論了這些風險因素。
神經感知生物技術有限公司(NeuroSense Therapeutics Ltd.)作爲一家外國私人發行人,宣佈截至2024年10月,已完成其爲期18個月的PARADIGm第20億ALS臨床試驗的給藥計劃。公司已達到最後受試者最後訪視的重要里程碑,正準備在2024年12月初公佈全面研究的頭條臨床結果。這些信息已在其提交給美國證券交易委員會(SEC)的6-k表格中披露。該報告還被作爲參考併入公司現有的S-8和F-3表格的註冊聲明中。神經感知生物技術已警告稱,該報告包含前瞻性聲明,可能受到風險和不確定性的影響,實際結果可能與預期有所不同。這些聲明包括報告臨床試驗結果的預期時間表,以及與FDA和加拿大衛生部等監管機構的討論。公司在其備案中概述了潛在的風險,包括延遲報告結果、意外研發成本和其產品候選者PrimeC的功效和安全性。公司在2024年4月4日向SEC提交的最新20-F年度報告詳細討論了這些風險因素。

譯文內容由第三人軟體翻譯。


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