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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:年度报告/过渡报告/注册声明
美股sec公告 ·  04/20 00:49
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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.
临床阶段的生物制药公司Biodexa Pharmaceuticals报告称,截至2023年12月31日的年度合并亏损708万英镑,经营活动产生的负现金流为683万英镑。该公司的财务业绩反映了其在推进其投资组合时对研发的巨额投资,包括用于1型糖尿病的托利米酮和用于罕见/孤儿脑癌的 MTX110。该年度的收入为38.1万英镑,较上一年的69.9万英镑有所下降。该公司的财务报表是在假设其将继续作为持续经营企业编制的,尽管经常性亏损和净资本短缺使人们对这种能力产生了极大的怀疑。Biodexa Pharmaceuticals的战略侧重于在寻找许可合作伙伴之前开发临床阶段资产以进行概念验证。该公司依赖第三方制造商提供临床试验材料,不打算建立自己的制造能力。Biodexa Pharmicals的候选产品受到包括美国食品药品管理局和欧洲药品管理局在内的政府机构的广泛监管。该公司未来的成功取决于获得必要的监管批准及其候选产品的商业化。
临床阶段的生物制药公司Biodexa Pharmaceuticals报告称,截至2023年12月31日的年度合并亏损708万英镑,经营活动产生的负现金流为683万英镑。该公司的财务业绩反映了其在推进其投资组合时对研发的巨额投资,包括用于1型糖尿病的托利米酮和用于罕见/孤儿脑癌的 MTX110。该年度的收入为38.1万英镑,较上一年的69.9万英镑有所下降。该公司的财务报表是在假设其将继续作为持续经营企业编制的,尽管经常性亏损和净资本短缺使人们对这种能力产生了极大的怀疑。Biodexa Pharmaceuticals的战略侧重于在寻找许可合作伙伴之前开发临床阶段资产以进行概念验证。该公司依赖第三方制造商提供临床试验材料,不打算建立自己的制造能力。Biodexa Pharmicals的候选产品受到包括美国食品药品管理局和欧洲药品管理局在内的政府机构的广泛监管。该公司未来的成功取决于获得必要的监管批准及其候选产品的商业化。

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