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用于开发长效凝血因子VIII的脂质体方法。

Liposomal approach towards the development of a longer-acting factor VIII.

作者信息

Powell J S

机构信息

UC Davis Hemophilia Treatment Center, University of California, Davis Medical Center, Sacramento, CA, USA.

出版信息

Haemophilia. 2007 Sep;13 Suppl 2:23-8. doi: 10.1111/j.1365-2516.2007.01502.x.

Abstract

Prevention of spontaneous bleeding in patients with severe haemophilia A usually requires therapeutic infusions every 2-3 days because of the short half-life of factor VIII (FVIII). Longer-acting FVIII products that require less frequent infusions would be beneficial and might obviate the need for central catheters in most patients. Liposomal formulation can enhance the efficacy of some therapeutic products. The incorporation of high-molecular weight polyethylene glycol (PEG) can extend the circulatory half-life of the liposome. These combined approaches led to the development of BAY 79-4,980, a PEG-containing liposomal version of Kogenate FS (rFVIII-FS). Results from preclinical models and early clinical trials have shown that BAY 79-4,980 prolongs the time to the next bleed. Further clinical evaluation of the efficacy and long-term safety of BAY 79-4,980 are planned.

摘要

由于凝血因子VIII(FVIII)半衰期较短,重度A型血友病患者预防自发性出血通常需要每2 - 3天进行一次治疗性输注。输注频率较低的长效FVIII产品将有益处,并且可能使大多数患者无需使用中心静脉导管。脂质体制剂可增强某些治疗产品的疗效。高分子量聚乙二醇(PEG)的掺入可延长脂质体的循环半衰期。这些联合方法促成了BAY 79 - 4,980的研发,它是含PEG的Kogenate FS(重组FVIII - FS)脂质体版本。临床前模型和早期临床试验的结果表明,BAY 79 - 4,980可延长至下次出血的时间。计划对BAY 79 - 4,980的疗效和长期安全性进行进一步临床评估。

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