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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...

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Autores principales: Rudd, Deanne Jackson, Zhang, Saijuan, Fillgrove, Kerry L., Fox‐Bosetti, Sabrina, Matthews, Randolph P., Friedman, Evan, Armas, Danielle, Stoch, S. Aubrey, Iwamoto, Marian
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2021
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.
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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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