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

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

XORTX Therapeutics | 6-K:外国发行人报告(业绩相关)
美股SEC公告 ·  2024/09/13 13:22

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XORTX Therapeutics has refiled its Management's Discussion and Analysis (MD&A) for the financial year ended December 31, 2023, and the interim period ended June 30, 2024, following a review by the Alberta Securities Commission. The amended YE 2023 MD&A now includes a full definition of Disclosure Controls and Procedures as per NI 52-109, addressing the previously abbreviated version.The Q2 2024 MD&A update provides additional information on the use of funds for the company's product candidates and estimated costs in the Outlook section. These amendments, approved by the company's Board of Directors on September 12, 2024, do not reflect any events occurring after the original filing dates or update other information from the original documents.XORTX, a late-stage clinical pharmaceutical company, is developing innovative therapies for progressive kidney disease. Their lead program, XRx-008, targets ADPKD, while XRx-101 focuses on acute kidney injury associated with COVID-19. The company is also advancing a pre-clinical program, XRx-225, for Type 2 Diabetic Nephropathy.
XORTX Therapeutics has refiled its Management's Discussion and Analysis (MD&A) for the financial year ended December 31, 2023, and the interim period ended June 30, 2024, following a review by the Alberta Securities Commission. The amended YE 2023 MD&A now includes a full definition of Disclosure Controls and Procedures as per NI 52-109, addressing the previously abbreviated version.The Q2 2024 MD&A update provides additional information on the use of funds for the company's product candidates and estimated costs in the Outlook section. These amendments, approved by the company's Board of Directors on September 12, 2024, do not reflect any events occurring after the original filing dates or update other information from the original documents.XORTX, a late-stage clinical pharmaceutical company, is developing innovative therapies for progressive kidney disease. Their lead program, XRx-008, targets ADPKD, while XRx-101 focuses on acute kidney injury associated with COVID-19. The company is also advancing a pre-clinical program, XRx-225, for Type 2 Diabetic Nephropathy.
XORTX Therapeutics已重新提交截至2023年12月31日的财务年度管理讨论和分析(MD&A)以及截至2024年6月30日的中期报告,此次提交经过阿尔伯塔证券委员会的审查。修订后的2023年MD&A现在根据NI 52-109包含了完整的披露控制和程序定义,解决了之前缩写版的问题。2024年第二季度MD&A更新提供了关于公司产品候选项目的资金使用和展望部分的估算成本的额外信息。这些修正案于2024年9月12日获得公司董事会的批准,并未反映原始提交日期后发生的事件或更新原始文件中的其他信息。XORTX是一家处于晚期临床阶段的药品公司,正在开发创新疗法以治疗进行性肾病。他们的主导项目XRx-008针对常染色体显性多囊肾病(ADPKD),而XRx-101则专注于与COVID-19相关的急性肾损伤。公司还在推动前临床项目XRx-225,以治疗2型糖尿病肾病。
XORTX Therapeutics已重新提交截至2023年12月31日的财务年度管理讨论和分析(MD&A)以及截至2024年6月30日的中期报告,此次提交经过阿尔伯塔证券委员会的审查。修订后的2023年MD&A现在根据NI 52-109包含了完整的披露控制和程序定义,解决了之前缩写版的问题。2024年第二季度MD&A更新提供了关于公司产品候选项目的资金使用和展望部分的估算成本的额外信息。这些修正案于2024年9月12日获得公司董事会的批准,并未反映原始提交日期后发生的事件或更新原始文件中的其他信息。XORTX是一家处于晚期临床阶段的药品公司,正在开发创新疗法以治疗进行性肾病。他们的主导项目XRx-008针对常染色体显性多囊肾病(ADPKD),而XRx-101则专注于与COVID-19相关的急性肾损伤。公司还在推动前临床项目XRx-225,以治疗2型糖尿病肾病。
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