Cargando…
A Mechanistic Model of Drug-Induced Liver Injury Aids the Interpretation of Elevated Liver Transaminase Levels in a Phase I Clinical Trial
Entolimod (CBLB502) is a Toll-like receptor 5 agonist in development as a single-dose countermeasure against total body irradiation. Efficacy can be assessed from animal studies, but the “Animal Rule” does not apply to safety assessment. Marked elevations of serum aminotransferases (exceeding 1,000...
Autores principales: | , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2014
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3944113/ https://www.ncbi.nlm.nih.gov/pubmed/24500662 http://dx.doi.org/10.1038/psp.2013.74 |
_version_ | 1782306332450226176 |
---|---|
author | Howell, B A Siler, S Q Shoda, L K M Yang, Y Woodhead, J L Watkins, P B |
author_facet | Howell, B A Siler, S Q Shoda, L K M Yang, Y Woodhead, J L Watkins, P B |
author_sort | Howell, B A |
collection | PubMed |
description | Entolimod (CBLB502) is a Toll-like receptor 5 agonist in development as a single-dose countermeasure against total body irradiation. Efficacy can be assessed from animal studies, but the “Animal Rule” does not apply to safety assessment. Marked elevations of serum aminotransferases (exceeding 1,000 IU/l) were observed in some human subjects receiving Entolimod in a safety study, threatening its continued development. The percentage of total hepatocytes undergoing necrosis in these subjects was estimated using a mechanistic, multiscale, mathematical model (DILIsym). The simulations suggested that no subject in the safety study experienced more than a modest loss of hepatocytes (<5%), which was comparable to estimates from a study of healthy volunteers receiving treatment with heparins. The predicted hepatocyte loss with Entolimod was lower than that required to cause liver dysfunction or that is routinely excised from volunteers donating for autologous liver transplantation and did not likely represent a serious health risk. |
format | Online Article Text |
id | pubmed-3944113 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-39441132014-03-06 A Mechanistic Model of Drug-Induced Liver Injury Aids the Interpretation of Elevated Liver Transaminase Levels in a Phase I Clinical Trial Howell, B A Siler, S Q Shoda, L K M Yang, Y Woodhead, J L Watkins, P B CPT Pharmacometrics Syst Pharmacol Original Article Entolimod (CBLB502) is a Toll-like receptor 5 agonist in development as a single-dose countermeasure against total body irradiation. Efficacy can be assessed from animal studies, but the “Animal Rule” does not apply to safety assessment. Marked elevations of serum aminotransferases (exceeding 1,000 IU/l) were observed in some human subjects receiving Entolimod in a safety study, threatening its continued development. The percentage of total hepatocytes undergoing necrosis in these subjects was estimated using a mechanistic, multiscale, mathematical model (DILIsym). The simulations suggested that no subject in the safety study experienced more than a modest loss of hepatocytes (<5%), which was comparable to estimates from a study of healthy volunteers receiving treatment with heparins. The predicted hepatocyte loss with Entolimod was lower than that required to cause liver dysfunction or that is routinely excised from volunteers donating for autologous liver transplantation and did not likely represent a serious health risk. Nature Publishing Group 2014-02 2014-02-05 /pmc/articles/PMC3944113/ /pubmed/24500662 http://dx.doi.org/10.1038/psp.2013.74 Text en Copyright © 2014 American Society for Clinical Pharmacology and Therapeutics http://creativecommons.org/licenses/by-nc-nd/3.0/ CPT: Pharmacometrics and Systems Pharmacology is an open-access journal published by Nature Publishing Group. This work is licensed under a Creative Commons Attribution-Noncommercial-No Derivative Works 3.0 License. To view a copy of this license, visit http://creativecommons.org/licenses/by-nc-nd/3.0/ |
spellingShingle | Original Article Howell, B A Siler, S Q Shoda, L K M Yang, Y Woodhead, J L Watkins, P B A Mechanistic Model of Drug-Induced Liver Injury Aids the Interpretation of Elevated Liver Transaminase Levels in a Phase I Clinical Trial |
title | A Mechanistic Model of Drug-Induced Liver Injury Aids the Interpretation of Elevated Liver Transaminase Levels in a Phase I Clinical Trial |
title_full | A Mechanistic Model of Drug-Induced Liver Injury Aids the Interpretation of Elevated Liver Transaminase Levels in a Phase I Clinical Trial |
title_fullStr | A Mechanistic Model of Drug-Induced Liver Injury Aids the Interpretation of Elevated Liver Transaminase Levels in a Phase I Clinical Trial |
title_full_unstemmed | A Mechanistic Model of Drug-Induced Liver Injury Aids the Interpretation of Elevated Liver Transaminase Levels in a Phase I Clinical Trial |
title_short | A Mechanistic Model of Drug-Induced Liver Injury Aids the Interpretation of Elevated Liver Transaminase Levels in a Phase I Clinical Trial |
title_sort | mechanistic model of drug-induced liver injury aids the interpretation of elevated liver transaminase levels in a phase i clinical trial |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3944113/ https://www.ncbi.nlm.nih.gov/pubmed/24500662 http://dx.doi.org/10.1038/psp.2013.74 |
work_keys_str_mv | AT howellba amechanisticmodelofdruginducedliverinjuryaidstheinterpretationofelevatedlivertransaminaselevelsinaphaseiclinicaltrial AT silersq amechanisticmodelofdruginducedliverinjuryaidstheinterpretationofelevatedlivertransaminaselevelsinaphaseiclinicaltrial AT shodalkm amechanisticmodelofdruginducedliverinjuryaidstheinterpretationofelevatedlivertransaminaselevelsinaphaseiclinicaltrial AT yangy amechanisticmodelofdruginducedliverinjuryaidstheinterpretationofelevatedlivertransaminaselevelsinaphaseiclinicaltrial AT woodheadjl amechanisticmodelofdruginducedliverinjuryaidstheinterpretationofelevatedlivertransaminaselevelsinaphaseiclinicaltrial AT watkinspb amechanisticmodelofdruginducedliverinjuryaidstheinterpretationofelevatedlivertransaminaselevelsinaphaseiclinicaltrial AT howellba mechanisticmodelofdruginducedliverinjuryaidstheinterpretationofelevatedlivertransaminaselevelsinaphaseiclinicaltrial AT silersq mechanisticmodelofdruginducedliverinjuryaidstheinterpretationofelevatedlivertransaminaselevelsinaphaseiclinicaltrial AT shodalkm mechanisticmodelofdruginducedliverinjuryaidstheinterpretationofelevatedlivertransaminaselevelsinaphaseiclinicaltrial AT yangy mechanisticmodelofdruginducedliverinjuryaidstheinterpretationofelevatedlivertransaminaselevelsinaphaseiclinicaltrial AT woodheadjl mechanisticmodelofdruginducedliverinjuryaidstheinterpretationofelevatedlivertransaminaselevelsinaphaseiclinicaltrial AT watkinspb mechanisticmodelofdruginducedliverinjuryaidstheinterpretationofelevatedlivertransaminaselevelsinaphaseiclinicaltrial |