Effect of Pevonedistat, an Investigational NEDD8-Activating Enzyme Inhibitor, on the QTc Interval in Patients With Advanced Solid Tumors

被引:3
|
作者
Zhou, Xiaofei [1 ]
Richardson, Debra L. [2 ,3 ]
Dowlati, Afshin [4 ]
Goel, Sanjay [5 ,11 ]
Sahebjam, Solmaz [6 ,12 ]
Strauss, James [7 ]
Chawla, Sant [8 ]
Wang, Ding [9 ]
Mould, Diane R. [10 ]
Samnotra, Vivek [1 ,13 ]
Faller, Douglas, V [1 ]
Venkatakrishnan, Karthik [1 ,14 ]
Gupta, Neeraj [1 ]
机构
[1] Takeda Dev Ctr Amer Inc TDCA, 40 Landsdowne St, Lexington, MA 02139 USA
[2] Univ Oklahoma, Stephenson Canc Ctr, Hlth Sci Ctr, Oklahoma City, OK USA
[3] Sarah Cannon Res Inst, Oklahoma City, OK USA
[4] Case Western Reserve Univ, Cleveland, OH 44106 USA
[5] Montefiore Med Ctr, 111 E 210th St, Bronx, NY 10467 USA
[6] Univ S Florida, H Lee Moffitt Canc Ctr & Res Inst, Tampa, FL USA
[7] Mary Crowley Canc Res, Dallas, TX USA
[8] Sarcoma Oncol Ctr, Santa Monica, CA USA
[9] Henry Ford Hosp, Detroit, MI 48202 USA
[10] Project Res Inc, Phoenixville, PA USA
[11] Rutgers Canc Inst New Jersey, New Brunswick, NJ USA
[12] NCI, NIH, Bethesda, MD USA
[13] GlaxoSmithKline Res & Dev Ltd, Waltham, MA USA
[14] EMD Serono Res & Dev Inst Inc, Billerica, MA USA
来源
CLINICAL PHARMACOLOGY IN DRUG DEVELOPMENT | 2023年 / 12卷 / 03期
关键词
NEDD8-activating enzyme inhibitor; pevonedistat; pharmacokinetics; QTc interval; PHASE-I; DRUGS; RISK; TAK-924/MLN4924; PROLONGATION;
D O I
10.1002/cpdd.1194
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
The purpose of this study was to assess the effect of pevonedistat, a neural precursor cell expressed, developmentally down-regulated protein 8 (NEDD8)-activating enzyme inhibitor, on the heart rate-corrected QT (QTc) interval in cancer patients. Patients were randomized 1:1 to receive pevonedistat 25 or 50 mg/m(2) on day 1 and the alternate dose on day 8. Triplicate electrocardiograms were collected at intervals over 0-11 hours and at 24 hours via Holter recorders on days -1 (baseline), 1, and 8. Changes from time-matched baseline values were calculated for QTc by Fridericia (QTcF), PR, and QRS intervals. Serial time-matched blood samples for analysis of pevonedistat plasma pharmacokinetics were collected and a concentration-QTc analysis conducted. Safety was assessed by monitoring vital signs, physical examinations, and clinical laboratory tests. Forty-four patients were included in the QTc analysis. Maximum least square (LS) mean increase from time-matched baseline in QTcF was 3.2 milliseconds at 1 hour postdose for pevonedistat at 25 mg/m(2), while the LSs mean change from baseline in QTcF was -1.7 milliseconds 1 hour postdose at 50 mg/m(2). The maximum 2-sided 90% upper confidence bound was 6.7 and 2.9 milliseconds for pevonedistat at 25 and 50 mg/m(2), respectively. Pevonedistat did not result in clinically relevant effects on heart rate, nor on PR or QRS intervals. Results from pevonedistat concentration-QTc analysis were consistent with these findings. Administration of pevonedistat to cancer patients at a dose of up to 50 mg/m(2) showed no evidence of QT prolongation, indicative of the lack of clinically meaningful effects on cardiac repolarization. ClinicalTrials.gov identifier: NCT03330106 (first registered on November 6, 2017).
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页码:257 / 266
页数:10
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