Exposure-response analysis to assess the concentration-QTc relationship of CC-122

被引:9
作者
Li, Yan [1 ]
Carayannopoulos, Leonidas N. [1 ]
Thomas, Michael [1 ]
Palmisano, Maria [1 ]
Zhou, Simon [1 ]
机构
[1] Celgene Corp, Translat Dev & Clin Pharmacol, 86 Morris Ave, Summit, NJ 07920 USA
关键词
cardiovascular assessment; QT prolongation effect;
D O I
10.2147/CPAA.S111867
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
CC-122 hydrochloride is a novel pleiotropic pathway modifier compound that binds cereblon, a substrate receptor of the Cullin 4 RING E3 ubiquitin ligase complex. CC-122 has multiple activities including modulation of immune cells, antiproliferative activity of multiple myeloma and lymphoma cells, and antiangiogenic activity. CC-122 is being developed as an oncology treatment for hematologic malignancies and advanced solid tumors. Cardiovascular and vital sign assessments of CC-122 have been conducted in hERG assays in vitro and in a 28-day good laboratory practice monkey study with negative signals. To assess the potential concentration-QTc relationship in humans and to ascertain or exclude a small QT effect by CC-122, a plasma concentration exposure-and Delta QTcF-response model of CC-122 was developed. Intensive CC-122 concentration and paired triplicate electrocardiogram data from a single ascending dose study were included in the analysis. The parameters included in the final linear exposure-response model are intercept, slope, and treatment effect. The slope estimate of 0.0201 with 90% CI of (0.009, 0.035) indicates a weak relationship between Delta QTcF and CC-122 concentration. The upper bounds of the 90% CI of the model-predicted Delta Delta QTcF effect at C-max from the 4 mg clinical dose and the supratherapeutic dose of 15 mg (1.18 ms and 8.76 ms, respectively) are <10 ms threshold, suggesting that the risk of CC-122 QT prolongation effect at the relevant therapeutic dose range from 1 mg to 4 mg is low.
引用
收藏
页码:117 / 125
页数:9
相关论文
共 13 条
[1]  
[Anonymous], 2015, ICH E14 GUID CLIN EV
[2]   The QT interval [J].
Bednar, MM ;
Harrigan, EP ;
Anziano, RJ ;
Camm, AJ ;
Ruskin, JN .
PROGRESS IN CARDIOVASCULAR DISEASES, 2001, 43 (05) :1-45
[3]   The prospective IQ-CSRC trial: A prototype early clinical proarrhythmia assessment investigation for replacing the ICH E14 thorough QTc (TQT) study [J].
Cavero, Icilio ;
Holzgrefe, Henry ;
Clements, Mike .
JOURNAL OF PHARMACOLOGICAL AND TOXICOLOGICAL METHODS, 2016, 80 :1-8
[4]   Lenalidomide at Therapeutic and Supratherapeutic Doses Does Not Prolong QTc Intervals in the Thorough QTc Study Conducted in Healthy Men [J].
Chen, Nianhang ;
Ye, Ying ;
Liu, Liangang ;
Reyes, Josephine ;
Assaf, Mahmoud S. ;
Kasserra, Claudia ;
Zhou, Simon ;
Palmisano, Maria .
BASIC & CLINICAL PHARMACOLOGY & TOXICOLOGY, 2013, 113 (03) :179-186
[5]   Results From the IQ-CSRC Prospective Study Support Replacement of the Thorough QT Study by QT Assessment in the Early Clinical Phase [J].
Darpo, B. ;
Benson, C. ;
Dota, C. ;
Ferber, G. ;
Garnett, C. ;
Green, C. L. ;
Jarugula, V. ;
Johannesen, L. ;
Keirns, J. ;
Krudys, K. ;
Liu, J. ;
Ortemann-Renon, C. ;
Riley, S. ;
Sarapa, N. ;
Smith, B. ;
Stoltz, R. R. ;
Zhou, M. ;
Stockbridge, N. .
CLINICAL PHARMACOLOGY & THERAPEUTICS, 2015, 97 (04) :326-335
[6]   The IQ-CSRC Prospective Clinical Phase 1 Study: "Can Early QT Assessment Using Exposure Response Analysis Replace the Thorough QT Study?" [J].
Darpo, Borje ;
Sarapa, Nenad ;
Garnett, Christine ;
Benson, Charles ;
Dota, Corina ;
Ferber, Georg ;
Jarugula, Venkateswar ;
Johannesen, Lars ;
Keirns, James ;
Krudys, Kevin ;
Ortemann-Renon, Catherine ;
Riley, Steve ;
Rogers-Subramaniam, Danise ;
Stockbridge, Norman .
ANNALS OF NONINVASIVE ELECTROCARDIOLOGY, 2014, 19 (01) :70-81
[7]  
European Medicines Agency (EMEA), 2005, CHMPICH204 EMEA
[8]   Exposure-response analysis of pertuzumab in HER2-positive metastatic breast cancer: absence of effect on QTc prolongation and other ECG parameters [J].
Garg, Amit ;
Li, Jing ;
Clark, Emma ;
Knott, Adam ;
Carrothers, Timothy J. ;
Marier, Jean-Francois ;
Cortes, Javier ;
Brewster, Michael ;
Visich, Jennifer ;
Lum, Bert .
CANCER CHEMOTHERAPY AND PHARMACOLOGY, 2013, 72 (05) :1133-1141
[9]   Concentration-QT relationships play a key role in the evaluation of proarrhythmic risk during regulatory review [J].
Garnett, Christine E. ;
Beasley, Nhi ;
Bhattaram, V. Atul ;
Jadhav, Pravin R. ;
Madabushi, Rajanikanth ;
Stockbridge, Norman ;
Tornoe, Christoffer W. ;
Wang, Yaning ;
Zhu, Hao ;
Gobburu, Jogarao V. .
JOURNAL OF CLINICAL PHARMACOLOGY, 2008, 48 (01) :13-18
[10]   CC-122, a pleiotropic pathway modifier, mimics an interferon response and has antitumor activity in DLBCL [J].
Hagner, Patrick R. ;
Man, Hon-Wah ;
Fontanillo, Celia ;
Wang, Maria ;
Couto, Suzana ;
Breider, Mike ;
Bjorklund, Chad ;
Havens, Courtney G. ;
Lu, Gang ;
Rychak, Emily ;
Raymon, Heather ;
Narla, Rama Krishna ;
Barnes, Leo ;
Khambatta, Gody ;
Chiu, Hsiling ;
Kosek, Jolanta ;
Kang, Jian ;
Amantangelo, Michael D. ;
Waldman, Michelle ;
Lopez-Girona, Antonia ;
Cai, Ti ;
Pourdehnad, Michael ;
Trotter, Matthew ;
Daniel, Thomas O. ;
Schafer, Peter H. ;
Klippel, Anke ;
Thakurta, Anjan ;
Chopra, Rajesh ;
Gandhi, Anita K. .
BLOOD, 2015, 126 (06) :779-789