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The Effects of 2′-O-Methoxyethyl Containing Antisense Oligonucleotides on Platelets in Human Clinical Trials
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...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Mary Ann Liebert, Inc.
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5467133/ https://www.ncbi.nlm.nih.gov/pubmed/28145801 http://dx.doi.org/10.1089/nat.2016.0650 |
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author | Crooke, Stanley T. Baker, Brenda F. Witztum, Joseph L. Kwoh, T. Jesse Pham, Nguyen C. Salgado, Nelson McEvoy, Bradley W. Cheng, Wei Hughes, Steven G. Bhanot, Sanjay Geary, Richard S. |
author_facet | Crooke, Stanley T. Baker, Brenda F. Witztum, Joseph L. Kwoh, T. Jesse Pham, Nguyen C. Salgado, Nelson McEvoy, Bradley W. Cheng, Wei Hughes, Steven G. Bhanot, Sanjay Geary, Richard S. |
author_sort | Crooke, Stanley T. |
collection | PubMed |
description | 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 624 mg/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/μL 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/μL. 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. |
format | Online Article Text |
id | pubmed-5467133 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Mary Ann Liebert, Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-54671332017-06-14 The Effects of 2′-O-Methoxyethyl Containing Antisense Oligonucleotides on Platelets in Human Clinical Trials Crooke, Stanley T. Baker, Brenda F. Witztum, Joseph L. Kwoh, T. Jesse Pham, Nguyen C. Salgado, Nelson McEvoy, Bradley W. Cheng, Wei Hughes, Steven G. Bhanot, Sanjay Geary, Richard S. Nucleic Acid Ther Original Articles 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 624 mg/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/μL 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/μL. 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. Mary Ann Liebert, Inc. 2017-06-01 2017-06-01 /pmc/articles/PMC5467133/ /pubmed/28145801 http://dx.doi.org/10.1089/nat.2016.0650 Text en © Stanley T. Crooke et al. 2017; Published by Mary Ann Liebert, Inc. This article is available under the Creative Commons License CC-BY-NC (http://creativecommons.org/licenses/by-nc/4.0). This license permits non-commercial use, distribution and reproduction in any medium, provided the original work is properly cited. Permission only needs to be obtained for commercial use and can be done via RightsLink. |
spellingShingle | Original Articles Crooke, Stanley T. Baker, Brenda F. Witztum, Joseph L. Kwoh, T. Jesse Pham, Nguyen C. Salgado, Nelson McEvoy, Bradley W. Cheng, Wei Hughes, Steven G. Bhanot, Sanjay Geary, Richard S. The Effects of 2′-O-Methoxyethyl Containing Antisense Oligonucleotides on Platelets in Human Clinical Trials |
title | The Effects of 2′-O-Methoxyethyl Containing Antisense Oligonucleotides on Platelets in Human Clinical Trials |
title_full | The Effects of 2′-O-Methoxyethyl Containing Antisense Oligonucleotides on Platelets in Human Clinical Trials |
title_fullStr | The Effects of 2′-O-Methoxyethyl Containing Antisense Oligonucleotides on Platelets in Human Clinical Trials |
title_full_unstemmed | The Effects of 2′-O-Methoxyethyl Containing Antisense Oligonucleotides on Platelets in Human Clinical Trials |
title_short | The Effects of 2′-O-Methoxyethyl Containing Antisense Oligonucleotides on Platelets in Human Clinical Trials |
title_sort | effects of 2′-o-methoxyethyl containing antisense oligonucleotides on platelets in human clinical trials |
topic | Original Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5467133/ https://www.ncbi.nlm.nih.gov/pubmed/28145801 http://dx.doi.org/10.1089/nat.2016.0650 |
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