Zheng Ming, Burt David, Chan Wai, Hawthorne Dara, Gasior Maciej, Bhagwagar Zubin, Keswani Sanjay, AbuTarif Malaz, Bertz Richard
Exploratory Clinical and Translational Research, Bristol-Myers Squibb, Princeton, NJ, USA.
Global Biometric Sciences, Bristol-Myers Squibb, Princeton, NJ, USA.
J Clin Pharmacol. 2015 Oct;55(10):1137-46. doi: 10.1002/jcph.528. Epub 2015 Jun 9.
As BMS-820836 causes dose-dependent heart rate increases, QTcI, QTcF, QTcB, and QT beat-to-beat methods were compared in this thorough QT study in healthy subjects. Two parallel groups of subjects (n = 60 per group) received 2 mg (maximum therapeutic) or 4 mg (supratherapeutic) of BMS-820836 once daily for 14 days with uptitration. Another 60 subjects received encapsulated moxifloxacin (400 mg) or matching placebo in a nested-crossover study design. Compared with QTcF and QTcB, baseline QTcI had the smallest and near-zero Pearson correlation coefficient with heart rate (0.0938), which supported the choice of QTcI as the primary electrocardiographic end point. BMS-820836 was not associated with prolongation of the QT interval at the doses tested; however, ΔΔQTbtb showed the smallest deviation from 0 milliseconds compared with ΔΔQTcI and ΔΔQTcF. The ΔΔQTbtb results appeared to be more consistent with the very low likelihood of any effect on the QT interval by BMS-820836 based on the wide margin (>400×) of the in vitro hERG IC50 and free plasma concentration. Further, this is the first published study that used the nested-crossover design and QTbtb analysis in a thorough QT study. Assay sensitivity was confirmed with encapsulated moxifloxacin.
由于BMS-820836会导致剂量依赖性心率增加,因此在这项针对健康受试者的全面QT研究中,对QTcI、QTcF、QTcB和逐搏QT方法进行了比较。两组平行的受试者(每组n = 60)接受2毫克(最大治疗剂量)或4毫克(超治疗剂量)的BMS-820836,每日一次,共14天,并进行剂量递增。另外60名受试者在嵌套交叉研究设计中接受了莫西沙星胶囊(400毫克)或匹配的安慰剂。与QTcF和QTcB相比,基线QTcI与心率的Pearson相关系数最小且接近零(0.0938),这支持了选择QTcI作为主要心电图终点。在所测试的剂量下,BMS-820836与QT间期延长无关;然而,与ΔΔQTcI和ΔΔQTcF相比,ΔΔQTbtb与0毫秒的偏差最小。基于体外hERG IC50与游离血浆浓度的宽幅(>400倍),ΔΔQTbtb结果似乎与BMS-820836对QT间期产生任何影响的极低可能性更为一致。此外,这是第一项在全面QT研究中使用嵌套交叉设计和QTbtb分析的已发表研究。通过莫西沙星胶囊确认了检测灵敏度。