首页> 美国卫生研究院文献>Wiley-Blackwell Online Open >Lenalidomide at Therapeutic and Supratherapeutic Doses Does Not Prolong QTc Intervals in the Thorough QTc Study Conducted in Healthy Men
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Lenalidomide at Therapeutic and Supratherapeutic Doses Does Not Prolong QTc Intervals in the Thorough QTc Study Conducted in Healthy Men

机译:在健康男性进行的全面QTc研究中来那度胺的治疗和治疗剂量不会延长QTc间隔

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摘要

The effect of lenalidomide on the corrected QT (QTc) interval was evaluated in healthy men and extended to patients based on the lenalidomide concentration–QTc (C–QTc) relationship. A rigorous assessment of the effect of lenalidomide on QTc intervals was conducted in healthy volunteers who each received, in randomized order, a single oral dose of 10 mg lenalidomide, 50 mg lenalidomide, 400 mg moxifloxacin (positive control) and placebo. Plasma lenalidomide exposure was compared between healthy volunteers and patients with multiple myeloma or myelodysplastic syndromes. In healthy volunteers, moxifloxacin produced the expected significant prolongation in QTcI (individual correction). For lenalidomide 10 mg and 50 mg, the time-matched changes from placebo in the baseline-adjusted least-squares mean QTcI were <3 ms with the upper limit of the two-sided 90% confidence interval for the change <10 ms at all time-points. No subjects experienced QTcI >450 ms or change from baseline >60 ms after lenalidomide administration. Similar results were seen with QT interval data corrected by Fridericia and Bazett methods. The C–QTc analysis yielded no significant association between lenalidomide concentrations and QTcI changes up to 1522 ng/mL; this range was close to that observed in patients receiving lenalidomide doses up to 50 mg, including those with reduced drug clearance due to renal impairment. In conclusion, single doses of lenalidomide up to 50 mg were not associated with prolonged QTc intervals in healthy males. The C–QTc analysis further assured that lenalidomide doses up to 50 mg are not expected to prolong QTc intervals in patients.
机译:在健康男性中评估来那度胺对校正的QT(QTc)间隔的影响,并根据来那度胺浓度与QTc(C–QTc)的关系扩展至患者。在健康志愿者中对来那度胺对QTc间隔的影响进行了严格的评估,他们随机接受单次口服剂量的10mg来那度胺,50mg来那度胺,400mg莫西沙星(阳性对照)和安慰剂。在健康志愿者和患有多发性骨髓瘤或骨髓增生异常综合症的患者之间比较了来那度胺的血浆暴露水平。在健康志愿者中,莫西沙星在QTcI中产生了预期的显着延长(个体校正)。对于来那度胺10 mg和50 mg,在基线调整后的最小二乘均方中,安慰剂的时间匹配变化均值QTcI为<3 ms,而两侧90%置信区间的上限均<10 ms时间点。来那度胺给药后没有受试者经历QTcI> 450 ms或从基线> 60 ms变化。通过Fridericia和Bazett方法校正的QT间隔数据也看到了相似的结果。 C–QTc分析显示来那度胺浓度与高达1522 ng / mL的QTcI变化之间无显着关联;该范围接近接受来那度胺剂量最高50 mg的患者所观察到的范围,包括那些因肾功能不全而使药物清除率降低的患者。总之,在健康男性中单剂量来那度胺高达50 mg与延长QTc间隔无关。 C–QTc分析进一步确保了来那度胺剂量高达50 mg不会延长患者的QTc间隔。

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