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Lack of a Clinically Meaningful Drug Interaction Between the HIV‐1 Antiretroviral Agents Islatravir, Dolutegravir, and Tenofovir Disoproxil Fumarate
Islatravir, an investigational nucleoside reverse transcriptase translocation inhibitor, is in clinical development for the treatment and prevention of HIV‐1 infection. Because islatravir may be coadministered with other antiretroviral agents, assessment of potential drug‐drug interactions are warra...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9298070/ https://www.ncbi.nlm.nih.gov/pubmed/34676683 http://dx.doi.org/10.1002/cpdd.1026 |
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author | Rudd, Deanne Jackson Zhang, Saijuan Fillgrove, Kerry L. Fox‐Bosetti, Sabrina Matthews, Randolph P. Friedman, Evan Armas, Danielle Stoch, S. Aubrey Iwamoto, Marian |
author_facet | Rudd, Deanne Jackson Zhang, Saijuan Fillgrove, Kerry L. Fox‐Bosetti, Sabrina Matthews, Randolph P. Friedman, Evan Armas, Danielle Stoch, S. Aubrey Iwamoto, Marian |
author_sort | Rudd, Deanne Jackson |
collection | PubMed |
description | Islatravir, an investigational nucleoside reverse transcriptase translocation inhibitor, is in clinical development for the treatment and prevention of HIV‐1 infection. Because islatravir may be coadministered with other antiretroviral agents, assessment of potential drug‐drug interactions are warranted. This phase 1, open‐label, fixed‐sequence, 2‐period trial in adults without HIV (N = 12) assessed the safety and pharmacokinetic interactions of islatravir administered with dolutegravir and tenofovir disoproxil fumarate (TDF). In period 1, participants received a single oral dose of islatravir (20 mg). In period 2, participants received oral doses of dolutegravir (50 mg) and TDF (300 mg) once daily on days 1 through 11, with a single oral dose of islatravir (20 mg) coadministered on day 8. There were no clinically significant changes in islatravir, dolutegravir, or TDF pharmacokinetics following coadministration. Islatravir was generally well tolerated when administered alone or in combination with dolutegravir and TDF. Coadministration of islatravir, dolutegravir, and TDF is supported, with no clinically meaningful effect on pharmacokinetics, safety, or tolerability in participants without HIV. |
format | Online Article Text |
id | pubmed-9298070 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-92980702022-07-21 Lack of a Clinically Meaningful Drug Interaction Between the HIV‐1 Antiretroviral Agents Islatravir, Dolutegravir, and Tenofovir Disoproxil Fumarate Rudd, Deanne Jackson Zhang, Saijuan Fillgrove, Kerry L. Fox‐Bosetti, Sabrina Matthews, Randolph P. Friedman, Evan Armas, Danielle Stoch, S. Aubrey Iwamoto, Marian Clin Pharmacol Drug Dev Articles Islatravir, an investigational nucleoside reverse transcriptase translocation inhibitor, is in clinical development for the treatment and prevention of HIV‐1 infection. Because islatravir may be coadministered with other antiretroviral agents, assessment of potential drug‐drug interactions are warranted. This phase 1, open‐label, fixed‐sequence, 2‐period trial in adults without HIV (N = 12) assessed the safety and pharmacokinetic interactions of islatravir administered with dolutegravir and tenofovir disoproxil fumarate (TDF). In period 1, participants received a single oral dose of islatravir (20 mg). In period 2, participants received oral doses of dolutegravir (50 mg) and TDF (300 mg) once daily on days 1 through 11, with a single oral dose of islatravir (20 mg) coadministered on day 8. There were no clinically significant changes in islatravir, dolutegravir, or TDF pharmacokinetics following coadministration. Islatravir was generally well tolerated when administered alone or in combination with dolutegravir and TDF. Coadministration of islatravir, dolutegravir, and TDF is supported, with no clinically meaningful effect on pharmacokinetics, safety, or tolerability in participants without HIV. John Wiley and Sons Inc. 2021-10-22 2021-12 /pmc/articles/PMC9298070/ /pubmed/34676683 http://dx.doi.org/10.1002/cpdd.1026 Text en © 2021 Merck Sharp & Dohme Corp. Clinical Pharmacology in Drug Development published by Wiley Periodicals LLC on behalf of American College of Clinical Pharmacology https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Articles Rudd, Deanne Jackson Zhang, Saijuan Fillgrove, Kerry L. Fox‐Bosetti, Sabrina Matthews, Randolph P. Friedman, Evan Armas, Danielle Stoch, S. Aubrey Iwamoto, Marian Lack of a Clinically Meaningful Drug Interaction Between the HIV‐1 Antiretroviral Agents Islatravir, Dolutegravir, and Tenofovir Disoproxil Fumarate |
title | Lack of a Clinically Meaningful Drug Interaction Between the HIV‐1 Antiretroviral Agents Islatravir, Dolutegravir, and Tenofovir Disoproxil Fumarate |
title_full | Lack of a Clinically Meaningful Drug Interaction Between the HIV‐1 Antiretroviral Agents Islatravir, Dolutegravir, and Tenofovir Disoproxil Fumarate |
title_fullStr | Lack of a Clinically Meaningful Drug Interaction Between the HIV‐1 Antiretroviral Agents Islatravir, Dolutegravir, and Tenofovir Disoproxil Fumarate |
title_full_unstemmed | Lack of a Clinically Meaningful Drug Interaction Between the HIV‐1 Antiretroviral Agents Islatravir, Dolutegravir, and Tenofovir Disoproxil Fumarate |
title_short | Lack of a Clinically Meaningful Drug Interaction Between the HIV‐1 Antiretroviral Agents Islatravir, Dolutegravir, and Tenofovir Disoproxil Fumarate |
title_sort | lack of a clinically meaningful drug interaction between the hiv‐1 antiretroviral agents islatravir, dolutegravir, and tenofovir disoproxil fumarate |
topic | Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9298070/ https://www.ncbi.nlm.nih.gov/pubmed/34676683 http://dx.doi.org/10.1002/cpdd.1026 |
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