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polarmouse

铁虫 (初入文坛)

[求助] 求两段翻译,非常紧急,感激涕零

In open-label, randomized, three-period, three-treatment crossover studies, 10 subjects received 10 mg A, 45 mg B or the combination, while20 subjects received 20 mg A, 1000 mg C or the combination. In an open-label, randomized, five-period, five-treatment, unbalanced crossover study, 12 subjects first received 20 mg A, 4 mg D or the combination, and afterward 100 mg sitagliptin or sitagliptin plus 20 mg A. Blood samples were taken over 72 h of each treatmentperiod. Lack of PK interaction was defined as the ratio of geometric means and 90% confidence interval (CI) for combination:monotherapy being within the range of 0.80–1.25 。
   Co-administration of A withB, C or D had no effect on A maximum plasma concentration (Cmax) or area under the plasma concentration-time curve (AUC). Similarly, A did not affect the Cmax or AUC for the co-administered drug, except for slight extensions of the 90% CI for the ratio of geometric means for B AUC (upper limit 1.29) andC Cmax (lower limit 0.75). All monotherapies and combination therapies were well tolerated.
    A can be co-administered with B、C、Dwithout dose adjustment of either drug

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Mally89

铁杆木虫 (职业作家)

T_T

【答案】应助回帖

Blood samples were taken over 72 h of each treatment period. Lack of PK interaction was defined as the ratio of geometric means and 90% confidence interval (CI) for combination:monotherapy being within the range of 0.80–1.25 。
每个处理周期72小时之后将血液样本取出。根据几何方法和混合物90%置信区间(在0.8-1.25范围内的单一治疗)的比值来判定交叉反应中是否缺乏PK。
6楼2011-05-08 16:09:08
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Mally89

铁杆木虫 (职业作家)

T_T

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sltmac(金币+41, 翻译EPI+1): 2011-05-16 07:52:15
sltmac: 继续努力~~ 2011-05-16 07:52:30
In open-label, randomized, three-period, three-treatment crossover studies, 10 subjects received 10 mg A, 45 mg B or the combination, while20 subjects received 20 mg A, 1000 mg C or the combination. In an open-label, randomized, five-period, five-treatment, unbalanced crossover study, 12 subjects first received 20 mg A, 4 mg D or the combination, and afterward 100 mg sitagliptin or sitagliptin plus 20 mg A。
在进行持续三个周期,随机开放标记的三个处理交叉治疗研究当中,10个样本中加入10mg的A,45mg的B或者二者的混合物,另外20个样本中加入20mg的A、1000mg的C或者二者的混合物。在另一个随机开放标记,维持5个周期的5个交叉不平衡处理研究当中,首先向12个样本中加入20mg A,4mg D或者二者混合物,然后再加入100mg西他列汀或加有20mgA的西他列汀。
5楼2011-05-08 15:22:48
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