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On January 22, 2024, Biodexa Pharmaceuticals PLC, a clinical stage biopharmaceutical company, issued a shareholder letter through CEO and CFO Stephen Stamp, outlining the company's achievements in 2023 and its strategic outlook for 2024. The letter, which serves as a progress report, was released as part of a Form 6-K filing with the United States Securities and Exchange Commission. Biodexa, which transitioned from Midatech Pharma to a NASDAQ-listed entity with a broader therapeutic portfolio, highlighted the in-licensing of tolimidone, a clinical stage molecule for Type 1 diabetes. The company plans to announce data from an in vitro study of tolimidone and initiate a Phase IIa study in 2024. Additionally, Biodexa reported on MTX110, a treatment for recurrent Glioblastoma Multiforme and Diffuse Midline Glioma, with...Show More
On January 22, 2024, Biodexa Pharmaceuticals PLC, a clinical stage biopharmaceutical company, issued a shareholder letter through CEO and CFO Stephen Stamp, outlining the company's achievements in 2023 and its strategic outlook for 2024. The letter, which serves as a progress report, was released as part of a Form 6-K filing with the United States Securities and Exchange Commission. Biodexa, which transitioned from Midatech Pharma to a NASDAQ-listed entity with a broader therapeutic portfolio, highlighted the in-licensing of tolimidone, a clinical stage molecule for Type 1 diabetes. The company plans to announce data from an in vitro study of tolimidone and initiate a Phase IIa study in 2024. Additionally, Biodexa reported on MTX110, a treatment for recurrent Glioblastoma Multiforme and Diffuse Midline Glioma, with expected data announcements in 2024. Another focus is MTD217, targeting leptomeningeal disease, with preclinical data expected by the end of the first quarter of 2024. Biodexa raised $6.0 million in December 2023, which will support the delivery of preclinical and clinical data for its pipeline that includes five programs, four of which are at the clinical stage. The company's R&D facility is based in Cardiff, UK.
2024年1月22日，臨床階段的生物製藥公司Biodexa Pharmaceuticals PLC通過首席執行官兼首席財務官斯蒂芬·斯坦普發佈了一封股東信，概述了該公司在2023年的成就及其2024年的戰略展望。這封信是進展報告，是作爲向美國證券交易委員會提交的6-K表格的一部分發布的。Biodexa從Midatech Pharma過渡到一家擁有更廣泛治療產品組合的納斯達克上市實體，該公司強調了1型糖尿病臨床階段分子託利米酮的許可情況。該公司計劃公佈一項託利米酮體外研究的數據，並於2024年啓動一項IIa期研究。此外，Biodexa報告了治療複發性多形膠質母細胞瘤和瀰漫性中線神經膠質瘤的 MT...展開全部
2024年1月22日，臨床階段的生物製藥公司Biodexa Pharmaceuticals PLC通過首席執行官兼首席財務官斯蒂芬·斯坦普發佈了一封股東信，概述了該公司在2023年的成就及其2024年的戰略展望。這封信是進展報告，是作爲向美國證券交易委員會提交的6-K表格的一部分發布的。Biodexa從Midatech Pharma過渡到一家擁有更廣泛治療產品組合的納斯達克上市實體，該公司強調了1型糖尿病臨床階段分子託利米酮的許可情況。該公司計劃公佈一項託利米酮體外研究的數據，並於2024年啓動一項IIa期研究。此外，Biodexa報告了治療複發性多形膠質母細胞瘤和瀰漫性中線神經膠質瘤的 MTX110，預計將在2024年公佈數據。另一個重點是針對輕腦膜病的 MTD217，預計在 2024 年第一季度末公佈臨床前數據。Biodexa在2023年12月籌集了600萬美元，這將支持其產品線的臨床前和臨床數據的交付，其中包括五個項目，其中四個處於臨床階段。該公司的研發設施位於英國加的夫。
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