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Long-acting injectable antiretrovirals for HIV treatment and prevention
PURPOSE OF REVIEW: Long-acting antiretroviral (ARV) drugs may improve adherence to therapy and extend opportunities for therapeutic or prophylactic intervention to underserved patient populations. This review focuses on recent advances in the development of small molecule long-acting injectable ARV...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Lippincott Williams & Wilkins
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3815009/ https://www.ncbi.nlm.nih.gov/pubmed/24100877 http://dx.doi.org/10.1097/COH.0000000000000002 |
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author | Spreen, William R. Margolis, David A. Pottage, John C. |
author_facet | Spreen, William R. Margolis, David A. Pottage, John C. |
author_sort | Spreen, William R. |
collection | PubMed |
description | PURPOSE OF REVIEW: Long-acting antiretroviral (ARV) drugs may improve adherence to therapy and extend opportunities for therapeutic or prophylactic intervention to underserved patient populations. This review focuses on recent advances in the development of small molecule long-acting injectable ARV agents. RECENT FINDINGS: The need for combination ART and physicochemical and dosing limitations of current ARV drugs impede attempts to redevelop them as long-acting injectable formulations. However, the intrinsic properties of rilpivirine, a nonnucleoside reverse transcriptase inhibitor, and GSK1265744, an HIV-1 integrase strand transfer inhibitor, have enabled crystalline nanoparticle formulations to progress to clinical trials. SUMMARY: Investigational long-acting injectable nanoformulations of rilpivirine and GSK1265744 are clinical-stage development candidates. Complementary pharmacologic properties of both agents – different mechanisms of action, resistance profiles, metabolic pathways, lack of drug interactions and low daily oral doses – offer the potential for combination use. Phase I studies of the pharmacokinetics and safety of each long-acting formulation alone and in combination indicate that a monthly dosing regimen is possible for HIV treatment. An ongoing phase IIb trial of oral GSK1265744 and oral rilpivirine is evaluating this two-drug regimen for maintenance of virologic suppression; results will inform future studies using the injectable formulations. Additional preclinical and clinical studies indicate a potential use of each agent for HIV pre-exposure prophylaxis. |
format | Online Article Text |
id | pubmed-3815009 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | Lippincott Williams & Wilkins |
record_format | MEDLINE/PubMed |
spelling | pubmed-38150092013-11-04 Long-acting injectable antiretrovirals for HIV treatment and prevention Spreen, William R. Margolis, David A. Pottage, John C. Curr Opin HIV AIDS TREATMENT OPTIMISATION: Edited by David H. Brown Ripin, Charles W. Flexner and Ben Plumley PURPOSE OF REVIEW: Long-acting antiretroviral (ARV) drugs may improve adherence to therapy and extend opportunities for therapeutic or prophylactic intervention to underserved patient populations. This review focuses on recent advances in the development of small molecule long-acting injectable ARV agents. RECENT FINDINGS: The need for combination ART and physicochemical and dosing limitations of current ARV drugs impede attempts to redevelop them as long-acting injectable formulations. However, the intrinsic properties of rilpivirine, a nonnucleoside reverse transcriptase inhibitor, and GSK1265744, an HIV-1 integrase strand transfer inhibitor, have enabled crystalline nanoparticle formulations to progress to clinical trials. SUMMARY: Investigational long-acting injectable nanoformulations of rilpivirine and GSK1265744 are clinical-stage development candidates. Complementary pharmacologic properties of both agents – different mechanisms of action, resistance profiles, metabolic pathways, lack of drug interactions and low daily oral doses – offer the potential for combination use. Phase I studies of the pharmacokinetics and safety of each long-acting formulation alone and in combination indicate that a monthly dosing regimen is possible for HIV treatment. An ongoing phase IIb trial of oral GSK1265744 and oral rilpivirine is evaluating this two-drug regimen for maintenance of virologic suppression; results will inform future studies using the injectable formulations. Additional preclinical and clinical studies indicate a potential use of each agent for HIV pre-exposure prophylaxis. Lippincott Williams & Wilkins 2013-11 2013-10-16 /pmc/articles/PMC3815009/ /pubmed/24100877 http://dx.doi.org/10.1097/COH.0000000000000002 Text en © 2013 Wolters Kluwer Health | Lippincott Williams & Wilkins http://creativecommons.org/licenses/by-nc-nd/3.0 This is an open-access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivitives 3.0 License, where it is permissible to download and share the work provided it is properly cited. The work cannot be changed in any way or used commercially. |
spellingShingle | TREATMENT OPTIMISATION: Edited by David H. Brown Ripin, Charles W. Flexner and Ben Plumley Spreen, William R. Margolis, David A. Pottage, John C. Long-acting injectable antiretrovirals for HIV treatment and prevention |
title | Long-acting injectable antiretrovirals for HIV treatment and prevention |
title_full | Long-acting injectable antiretrovirals for HIV treatment and prevention |
title_fullStr | Long-acting injectable antiretrovirals for HIV treatment and prevention |
title_full_unstemmed | Long-acting injectable antiretrovirals for HIV treatment and prevention |
title_short | Long-acting injectable antiretrovirals for HIV treatment and prevention |
title_sort | long-acting injectable antiretrovirals for hiv treatment and prevention |
topic | TREATMENT OPTIMISATION: Edited by David H. Brown Ripin, Charles W. Flexner and Ben Plumley |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3815009/ https://www.ncbi.nlm.nih.gov/pubmed/24100877 http://dx.doi.org/10.1097/COH.0000000000000002 |
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