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Highly stable compositions of orally active nucleotide analogs or orally active nucleotide analog prodrugs

机译:口服活性核苷酸类似物或口服活性核苷酸类似物前药的高度稳定的组合物

摘要

Disclosed are highly stable compositions having outstanding storage stability and/or demonstrating exceptional resistance to aqueous solution degradation, the composition including an orally active nucleotide analog or an orally active nucleotide analog prodrug, which is orally bioavailable, such as adefovir dipivoxil and tenofovir disoproxil. For example, when a composition of the invention is stored for 1 month or for 18 months at 25° C. and 60% relative humidity, its orally active nucleotide analog or orally active nucleotide analog prodrug degrades to provide a composition containing no more than 0.2% or no more than 0.7% by weight of a less orally bioavailable impurity, respectively. Also disclosed are a container/closure package system including the composition and a package insert and methods of manufacturing the composition and treating a patient for a disease or condition, for example, a viral disease or cancer, with the use of the composition.
机译:公开了具有优异的储存稳定性和/或表现出对水溶液降解的优异抗性的高度稳定的组合物,该组合物包括可口服生物利用的口服活性核苷酸类似物或口服活性核苷酸类似物前药,例如阿德福韦酯和替诺福韦二甲酚。例如,当本发明的组合物在25℃和60%相对湿度下存储1个月或18个月时,其口服活性核苷酸类似物或口服活性核苷酸类似物前药降解以提供包含不超过0.2的组合物。分别占口服生物利用度较少的杂质的1重量%或不超过0.7重量%。还公开了一种包括组合物和包装插页的容器/密闭包装系统,以及使用该组合物制造该组合物并治疗患者的疾病或病症例如病毒性疾病或癌症的方法。

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