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Model‐Informed Dosing of Venetoclax in Healthy Subjects: An Exposure−Response Analysis
Venetoclax is an approved drug for the treatment of some hematological malignancies. Venetoclax can cause reduction in B‐lymphocyte counts as an on‐target effect. The purpose of this analysis is to quantify the relationship between venetoclax exposure and B‐lymphocyte levels to inform dosing of vene...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6853148/ https://www.ncbi.nlm.nih.gov/pubmed/31268229 http://dx.doi.org/10.1111/cts.12665 |
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author | Dave, Nimita Gopalakrishnan, Sathej Mensing, Sven Salem, Ahmed Hamed |
author_facet | Dave, Nimita Gopalakrishnan, Sathej Mensing, Sven Salem, Ahmed Hamed |
author_sort | Dave, Nimita |
collection | PubMed |
description | Venetoclax is an approved drug for the treatment of some hematological malignancies. Venetoclax can cause reduction in B‐lymphocyte counts as an on‐target effect. The purpose of this analysis is to quantify the relationship between venetoclax exposure and B‐lymphocyte levels to inform dosing of venetoclax in healthy subjects. Data were pooled from 10 studies in healthy subjects with venetoclax doses ranging from 10 mg to 400 mg and food ranging from fasting to high‐fat meals. Venetoclax pharmacokinetics (PK) was characterized in 203 subjects using a population approach, as implemented in NONMEM version 7.3 (Icon Development Solutions, Ellicott City, MD, USA). A semimechanistic pharmacodynamic (PD) model with a linear drug effect was fit to the B‐lymphocyte data to determine the exposure‐response relationship. The population PK and PD model described the observed data adequately. The 200 and 400 mg doses were shown to reduce the B‐lymphocyte levels by 24% (15–35%) and 38% (25–54%), respectively. B‐lymphocytes recovered to normal levels within an average of 48 (21–64) days and 59 (30–66) days, respectively, with 200 and 400 mg doses. Venetoclax can be safely administered in healthy subjects. The PK‐PD model characterized the relationship between venetoclax exposure and reduction in B‐lymphocytes and will help design future venetoclax studies in healthy subjects. |
format | Online Article Text |
id | pubmed-6853148 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-68531482019-12-16 Model‐Informed Dosing of Venetoclax in Healthy Subjects: An Exposure−Response Analysis Dave, Nimita Gopalakrishnan, Sathej Mensing, Sven Salem, Ahmed Hamed Clin Transl Sci Research Venetoclax is an approved drug for the treatment of some hematological malignancies. Venetoclax can cause reduction in B‐lymphocyte counts as an on‐target effect. The purpose of this analysis is to quantify the relationship between venetoclax exposure and B‐lymphocyte levels to inform dosing of venetoclax in healthy subjects. Data were pooled from 10 studies in healthy subjects with venetoclax doses ranging from 10 mg to 400 mg and food ranging from fasting to high‐fat meals. Venetoclax pharmacokinetics (PK) was characterized in 203 subjects using a population approach, as implemented in NONMEM version 7.3 (Icon Development Solutions, Ellicott City, MD, USA). A semimechanistic pharmacodynamic (PD) model with a linear drug effect was fit to the B‐lymphocyte data to determine the exposure‐response relationship. The population PK and PD model described the observed data adequately. The 200 and 400 mg doses were shown to reduce the B‐lymphocyte levels by 24% (15–35%) and 38% (25–54%), respectively. B‐lymphocytes recovered to normal levels within an average of 48 (21–64) days and 59 (30–66) days, respectively, with 200 and 400 mg doses. Venetoclax can be safely administered in healthy subjects. The PK‐PD model characterized the relationship between venetoclax exposure and reduction in B‐lymphocytes and will help design future venetoclax studies in healthy subjects. John Wiley and Sons Inc. 2019-08-07 2019-11 /pmc/articles/PMC6853148/ /pubmed/31268229 http://dx.doi.org/10.1111/cts.12665 Text en © 2019 AbbVie Inc. Clinical and Translational Science published by Wiley Periodicals, Inc. on behalf of the American Society for Clinical Pharmacology and Therapeutics. This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made. |
spellingShingle | Research Dave, Nimita Gopalakrishnan, Sathej Mensing, Sven Salem, Ahmed Hamed Model‐Informed Dosing of Venetoclax in Healthy Subjects: An Exposure−Response Analysis |
title | Model‐Informed Dosing of Venetoclax in Healthy Subjects: An Exposure−Response Analysis |
title_full | Model‐Informed Dosing of Venetoclax in Healthy Subjects: An Exposure−Response Analysis |
title_fullStr | Model‐Informed Dosing of Venetoclax in Healthy Subjects: An Exposure−Response Analysis |
title_full_unstemmed | Model‐Informed Dosing of Venetoclax in Healthy Subjects: An Exposure−Response Analysis |
title_short | Model‐Informed Dosing of Venetoclax in Healthy Subjects: An Exposure−Response Analysis |
title_sort | model‐informed dosing of venetoclax in healthy subjects: an exposure−response analysis |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6853148/ https://www.ncbi.nlm.nih.gov/pubmed/31268229 http://dx.doi.org/10.1111/cts.12665 |
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