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Biodexa Pharmaceuticals | 20-F: Registration statement / Annual report / Transition report

Biodexa Pharmaceuticals | 20-F: Registration statement / Annual report / Transition report

Biodexa Pharmaceuticals | 20-F:年度報告/過渡報告/註冊聲明
美股sec公告 ·  04/19 12:49
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Biodexa Pharmaceuticals, a clinical-stage biopharmaceutical company, reported a consolidated loss of £7.08 million for the year ended December 31, 2023, with negative cash flows from operating activities amounting to £6.83 million. The company's financial performance reflects the significant investment in research and development as it advances its portfolio, including its lead assets tolimidone for Type 1 diabetes and MTX110 for rare/orphan brain cancers. Revenue for the year was £381,000, a decrease from the previous year's £699,000. The company's financial statements have been prepared under the assumption that it will continue as a going concern, despite the recurring losses and net capital deficiency raising substantial doubt about this ability. Biodexa Pharmaceuticals' strategy focuses on developing clinical-stage assets to proof-of-concept before seeking...Show More
Biodexa Pharmaceuticals, a clinical-stage biopharmaceutical company, reported a consolidated loss of £7.08 million for the year ended December 31, 2023, with negative cash flows from operating activities amounting to £6.83 million. The company's financial performance reflects the significant investment in research and development as it advances its portfolio, including its lead assets tolimidone for Type 1 diabetes and MTX110 for rare/orphan brain cancers. Revenue for the year was £381,000, a decrease from the previous year's £699,000. The company's financial statements have been prepared under the assumption that it will continue as a going concern, despite the recurring losses and net capital deficiency raising substantial doubt about this ability. Biodexa Pharmaceuticals' strategy focuses on developing clinical-stage assets to proof-of-concept before seeking licensing partners. The company relies on third-party manufacturers for clinical trial materials and does not plan to establish its own manufacturing capabilities. Biodexa Pharmaceuticals is subject to extensive regulation by government authorities, including the FDA and EMA, for its product candidates. The company's future success is dependent on obtaining necessary regulatory approvals and commercializing its product candidates.
臨床階段的生物製藥公司Biodexa Pharmaceuticals報告稱,截至2023年12月31日的年度合併虧損708萬英鎊,經營活動產生的負現金流爲683萬英鎊。該公司的財務業績反映了其在推進其投資組合時對研發的巨額投資,包括用於1型糖尿病的託利米酮和用於罕見/孤兒腦癌的 MTX110。該年度的收入爲38.1萬英鎊,較上一年的69.9萬英鎊有所下降。該公司的財務報表是在假設其將繼續作爲持續經營企業編制的,儘管經常性虧損和淨資本短缺使人們對這種能力產生了極大的懷疑。Biodexa Pharmaceuticals的戰略側重於在尋找許可合作伙伴之前開發臨床階段資產以進行概念驗證。該公司依賴第三方製造商提供臨床試驗材料,不打算建立自己的製造能力。Biodexa Pharmicals的候選產品受到包括美國食品藥品管理局和歐洲藥品管理局在內的政府機構的廣泛監管。該公司未來的成功取決於獲得必要的監管批准及其候選產品的商業化。
臨床階段的生物製藥公司Biodexa Pharmaceuticals報告稱,截至2023年12月31日的年度合併虧損708萬英鎊,經營活動產生的負現金流爲683萬英鎊。該公司的財務業績反映了其在推進其投資組合時對研發的巨額投資,包括用於1型糖尿病的託利米酮和用於罕見/孤兒腦癌的 MTX110。該年度的收入爲38.1萬英鎊,較上一年的69.9萬英鎊有所下降。該公司的財務報表是在假設其將繼續作爲持續經營企業編制的,儘管經常性虧損和淨資本短缺使人們對這種能力產生了極大的懷疑。Biodexa Pharmaceuticals的戰略側重於在尋找許可合作伙伴之前開發臨床階段資產以進行概念驗證。該公司依賴第三方製造商提供臨床試驗材料,不打算建立自己的製造能力。Biodexa Pharmicals的候選產品受到包括美國食品藥品管理局和歐洲藥品管理局在內的政府機構的廣泛監管。該公司未來的成功取決於獲得必要的監管批准及其候選產品的商業化。
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