The Effects of 2′-O-Methoxyethyl Containing Antisense Oligonucleotides on Platelets in Human Clinical Trials

被引:111
作者
Crooke, Stanley T. [1 ]
Baker, Brenda F. [1 ]
Witztum, Joseph L. [2 ]
Kwoh, Jesse [1 ]
Pham, Nguyen C. [1 ]
Salgado, Nelson [1 ]
McEvoy, Bradley W. [1 ]
Cheng, Wei [1 ]
Hughes, Steven G. [1 ]
Bhanot, Sanjay [1 ]
Geary, Richard S. [1 ]
机构
[1] Ionis Pharmaceut Inc, 2855 Gazelle Court, Carlsbad, CA 92011 USA
[2] Univ Calif San Diego, Sch Med, Dept Med, La Jolla, CA 92093 USA
关键词
antisense; safety; platelets; thrombocytopenia; factor XI; RESISTANT PROSTATE-CANCER; INTRINSIC TENASE COMPLEX; RANDOMIZED PHASE-II; CELL LUNG-CANCER; FACTOR-XI; DOUBLE-BLIND; FAMILIAL HYPERCHOLESTEROLEMIA; TARGETING APOLIPOPROTEIN(A); CUSTIRSEN OGX-011; DOSE-ESCALATION;
D O I
10.1089/nat.2016.0650
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
A thorough analysis of clinical trial data in the Ionis integrated safety database (ISDB) was performed to determine if there is a class effect on platelet numbers and function in subjects treated with 2'-O-methoxyethyl (2' MOE)-modified antisense oligonucleotides (ASOs). The Ionis ISDB includes over 2,600 human subjects treated with 16 different 2' MOE ASOs in placebo-controlled and open-label clinical trials over a range of doses up to 624mg/week and treatment durations as long as 4.6 years. This analysis showed that there is no class generic effect on platelet numbers and no incidence of confirmed platelet levels below 50 K/mL in subjects treated with 2' MOE ASOs. Only 7 of 2,638 (0.3%) subjects treated with a 2' MOE ASO experienced a confirmed postbaseline (BSLN) platelet count between 100 and 50 K/mL. Three of sixteen 2' MOE ASOs had > 10% incidence of platelet decreases > 30% from BSLN, suggesting that certain sequences may associate with clinically insignificant platelet declines. Further to these results, we found no evidence that 2' MOE ASOs alter platelet function, as measured by the lack of clinically relevant bleeding in the presence or absence of other drugs that alter platelet function and/or number and by the results from trials conducted with the factor XI (FXI) ASO.
引用
收藏
页码:121 / 129
页数:9
相关论文
共 34 条
[1]  
[Anonymous], 2015, 206031 FDA NDA
[2]   First-in-human Phase I study of EZN-4176, a locked nucleic acid antisense oligonucleotide to exon 4 of the androgen receptor mRNA in patients with castration-resistant prostate cancer [J].
Bianchini, D. ;
Omlin, A. ;
Pezaro, C. ;
Lorente, D. ;
Ferraldeschi, R. ;
Mukherji, D. ;
Crespo, M. ;
Figueiredo, I. ;
Miranda, S. ;
Riisnaes, R. ;
Zivi, A. ;
Buchbinder, A. ;
Rathkopf, D. E. ;
Attard, G. ;
Scher, H. I. ;
de Bono, J. ;
Danila, D. C. .
BRITISH JOURNAL OF CANCER, 2013, 109 (10) :2579-2586
[3]   Factor XI Antisense Oligonucleotide for Prevention of Venous Thrombosis [J].
Bueller, Harry R. ;
Bethune, Claudette ;
Bhanot, Sanjay ;
Gailani, David ;
Monia, Brett P. ;
Raskob, Gary E. ;
Segers, Annelise ;
Verhamme, Peter ;
Weitz, Jeffrey I. .
NEW ENGLAND JOURNAL OF MEDICINE, 2015, 372 (03) :232-240
[4]   Randomized Phase II Study of Docetaxel and Prednisone With or Without OGX-011 in Patients With Metastatic Castration-Resistant Prostate Cancer [J].
Chi, Kim N. ;
Hotte, Sebastien J. ;
Yu, Evan Y. ;
Tu, Dongsheng ;
Eigl, Bernhard J. ;
Tannock, Ian ;
Saad, Fred ;
North, Scott ;
Powers, Jean ;
Gleave, Martin E. ;
Eisenhauer, Elizabeth A. .
JOURNAL OF CLINICAL ONCOLOGY, 2010, 28 (27) :4247-4254
[5]   Phase II Trial of OGX-011 in Combination with Docetaxel in Metastatic Breast Cancer [J].
Chia, Stephen ;
Dent, Susan ;
Ellard, Susan ;
Ellis, Peter M. ;
Vandenberg, Ted ;
Gelmon, Karen ;
Powers, Jean ;
Walsh, Wendy ;
Seymour, Lesley ;
Eisenhauer, Elizabeth A. .
CLINICAL CANCER RESEARCH, 2009, 15 (02) :708-713
[6]  
Crooke S. T., 2007, Antisense drug technology: principles, strategies, and applications
[7]   Integrated Safety Assessment of 2′-O-Methoxyethyl Chimeric Antisense Oligonucleotides in NonHuman Primates and Healthy Human Volunteers [J].
Crooke, Stanley T. ;
Baker, Brenda F. ;
Kwoh, T. Jesse ;
Cheng, Wei ;
Schulz, Dan J. ;
Xia, Shuting ;
Salgado, Nelson ;
Bui, Huynh-Hoa ;
Hart, Christopher E. ;
Burel, Sebastien A. ;
Younis, Husam S. ;
Geary, Richard S. ;
Henry, Scott P. ;
Bhanot, Sanjay .
MOLECULAR THERAPY, 2016, 24 (10) :1771-1782
[8]   Antithrombotic Effect of Antisense Factor XI Oligonucleotide Treatment in Primates [J].
Crosby, Jeffrey R. ;
Marzec, Ulla ;
Revenko, Alexey S. ;
Zhao, Chenguang ;
Gao, Dacao ;
Matafonov, Anton ;
Gailani, David ;
MacLeod, A. Robert ;
Tucker, Erik I. ;
Gruber, Andras ;
Hanson, Stephen R. ;
Monia, Brett P. .
ARTERIOSCLEROSIS THROMBOSIS AND VASCULAR BIOLOGY, 2013, 33 (07) :1670-1678
[9]   Long-term mipomersen treatment is associated with a reduction in cardiovascular events in patients with familial hypercholesterolemia [J].
Duell, P. Barton ;
Santos, Raul D. ;
Kirwan, Bridget-Anne ;
Witztum, Joseph L. ;
Tsimikas, Sotirios ;
Kastelein, John J. P. .
JOURNAL OF CLINICAL LIPIDOLOGY, 2016, 10 (04) :1011-1021
[10]   Treatment of infantile-onset spinal muscular atrophy with nusinersen: a phase 2, open-label, dose-escalation study [J].
Finkel, Richard S. ;
Chiriboga, Claudia A. ;
Vajsar, Jiri ;
Day, John W. ;
Montes, Jacqueline ;
De Vivo, Darryl C. ;
Yamashita, Mason ;
Rigo, Frank ;
Hung, Gene ;
Schneider, Eugene ;
Norris, Daniel A. ;
Xia, Shuting ;
Bennett, C. Frank ;
Bishop, Kathie M. .
LANCET, 2016, 388 (10063) :3017-3026