首页> 美国卫生研究院文献>Journal of Therapeutic Ultrasound >Clinical trial protocol for TARDOX: a phase I study to investigate the feasibility of targeted release of lyso-thermosensitive liposomal doxorubicin (ThermoDox®) using focused ultrasound in patients with liver tumours
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Clinical trial protocol for TARDOX: a phase I study to investigate the feasibility of targeted release of lyso-thermosensitive liposomal doxorubicin (ThermoDox®) using focused ultrasound in patients with liver tumours

机译:TARDOX的临床试验方案:I期研究旨在通过聚焦超声在肝肿瘤患者中靶向溶酶热敏感性脂质体阿霉素(ThermoDox®)的靶向释放

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摘要

BackgroundTARDOX is a Phase I single center study of ultrasound triggered targeted drug delivery in adult oncology patients with incurable liver tumours. This proof of concept study is designed to demonstrate the safety and feasibility of targeted drug release and enhanced delivery of doxorubicin from thermally sensitive liposomes (ThermoDox®) triggered by mild hyperthermia induced by focused ultrasound in liver tumours. A key feature of the study is the direct quantification of the doxorubicin concentration before and after ultrasound exposure from tumour biopsies, using high performance liquid chromatography (HPLC).
机译:背景TARDOX是一项I期单中心研究,其研究对象为患有不可治愈的肝肿瘤的成年肿瘤患者,其超声触发了靶向药物的递送。这项概念验证研究旨在证明安全性和可行性,这种靶向性是由肝脏肿瘤中聚焦超声引起的轻度高温触发的热敏感脂质体(ThermoDox®)靶向释放药物和增强阿霉素的递送所致。该研究的关键特征是使用高效液相色谱法(HPLC)对来自肿瘤活检的超声暴露前后的阿霉素浓度进行直接定量。

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