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551. MK-8591 Does Not Alter the Pharmacokinetics of the Oral Contraceptives Ethinyl Estradiol and Levonorgestrel

BACKGROUND: Over 2 million girls and young women are living with HIV, being newly infected at disproportionately high rates. HIV infection adds risks to pregnancy, including vertical transmission and maternal death. Hormonal contraceptives are among the most effective reversible contraceptives, but...

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Autores principales: Ankrom, Wendy, Jonathan, Daniel, Rudd, Deanne, Zhang, Sandra, Fillgrove, Kerry, Gravesande, Kezia, Matthews, Randolph, Brimhall, Darin, Stoch, Aubrey, Iwamoto, Marian
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6255447/
http://dx.doi.org/10.1093/ofid/ofy210.559
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author Ankrom, Wendy
Jonathan, Daniel
Rudd, Deanne
Zhang, Sandra
Fillgrove, Kerry
Gravesande, Kezia
Matthews, Randolph
Brimhall, Darin
Stoch, Aubrey
Iwamoto, Marian
author_facet Ankrom, Wendy
Jonathan, Daniel
Rudd, Deanne
Zhang, Sandra
Fillgrove, Kerry
Gravesande, Kezia
Matthews, Randolph
Brimhall, Darin
Stoch, Aubrey
Iwamoto, Marian
author_sort Ankrom, Wendy
collection PubMed
description BACKGROUND: Over 2 million girls and young women are living with HIV, being newly infected at disproportionately high rates. HIV infection adds risks to pregnancy, including vertical transmission and maternal death. Hormonal contraceptives are among the most effective reversible contraceptives, but they have clinically meaningful drug–drug interactions (DDI) with many antiretrovirals (ARV). MK-8591 is a novel nucleoside reverse transcriptase translocation inhibitor (NRTTI) currently in Phase 2 clinical development for treatment of HIV. Unlike many ARVs, MK-8591 is not an inhibitor or inducer of major CYP enzymes and is not expected to alter the pharmacokinetics (PK) of hormonal contraceptives. This clinical study evaluated the DDI of MK-8591 with levonorgestrel (LNG) and ethinyl estradiol (EE) to support use of hormonal contraceptives with MK-8591. METHODS: This was an open-label, two-period, fixed-sequence DDI study in 14 healthy, postmenopausal or oopherectomized females aged 50–64. A single dose of LNG 0.15 mg/EE 0.03 mg was given followed by a 7-day washout. MK-8591 20 mg was then dosed once weekly for 3 weeks; a single dose of LNG 0.15 mg/EE 0.03 mg was given concomitantly with the third dose of MK-8591. PK samples were collected for evaluation of LNG and EE levels. Individual values of AUC0-inf and Cmax were natural log-transformed prior to analysis and evaluated separately using a linear mixed effects model with a fixed effects term for treatment. An unstructured covariance matrix was used to allow for unequal treatment variances and to model the correlation between the treatment measurements within each subject. RESULTS: The PK of EE and LNG were not meaningfully altered by co-administration with MK-8591. For the comparison of (MK-8591 + LNG/EE) / (LNG/EE alone), the geometric mean ratios (GMRs) (90% confidence intervals (CIs)) for LNG AUC0-inf and Cmax were 1.13 (1.06, 1.20) and 0.965 (0.881, 1.06), respectively. For EE the GMRs (90% CI) for AUC0-inf and Cmax were 1.05 (0.981, 1.11) and 1.02 (0.971, 1.08), respectively. Co-administration of all three drugs was generally well tolerated. CONCLUSION: The results of this study support use of hormonal contraceptives in HIV-infected patients receiving MK-8591. DISCLOSURES: W. Ankrom, Merck & Co, Inc.: Employee and Shareholder, Salary. D. Jonathan, Merck: Employee, Salary. D. Rudd, Merck & Co., INC.: Employee, Salary. S. Zhang, Merck & Co, Inc.: Employee, Salary. K. Fillgrove, Merck & Co., Inc.: Employee, Salary. K. Gravesande, Kezia Gravesande: Research Contractor, Salary. R. Matthews, Merck: Employee, Salary. A. Stoch, Merck & Co, Inc.: Employee and Shareholder, Salary. M. Iwamoto, Merck & Co, Inc.: Employee and Shareholder, Salary.
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spelling pubmed-62554472018-11-28 551. MK-8591 Does Not Alter the Pharmacokinetics of the Oral Contraceptives Ethinyl Estradiol and Levonorgestrel Ankrom, Wendy Jonathan, Daniel Rudd, Deanne Zhang, Sandra Fillgrove, Kerry Gravesande, Kezia Matthews, Randolph Brimhall, Darin Stoch, Aubrey Iwamoto, Marian Open Forum Infect Dis Abstracts BACKGROUND: Over 2 million girls and young women are living with HIV, being newly infected at disproportionately high rates. HIV infection adds risks to pregnancy, including vertical transmission and maternal death. Hormonal contraceptives are among the most effective reversible contraceptives, but they have clinically meaningful drug–drug interactions (DDI) with many antiretrovirals (ARV). MK-8591 is a novel nucleoside reverse transcriptase translocation inhibitor (NRTTI) currently in Phase 2 clinical development for treatment of HIV. Unlike many ARVs, MK-8591 is not an inhibitor or inducer of major CYP enzymes and is not expected to alter the pharmacokinetics (PK) of hormonal contraceptives. This clinical study evaluated the DDI of MK-8591 with levonorgestrel (LNG) and ethinyl estradiol (EE) to support use of hormonal contraceptives with MK-8591. METHODS: This was an open-label, two-period, fixed-sequence DDI study in 14 healthy, postmenopausal or oopherectomized females aged 50–64. A single dose of LNG 0.15 mg/EE 0.03 mg was given followed by a 7-day washout. MK-8591 20 mg was then dosed once weekly for 3 weeks; a single dose of LNG 0.15 mg/EE 0.03 mg was given concomitantly with the third dose of MK-8591. PK samples were collected for evaluation of LNG and EE levels. Individual values of AUC0-inf and Cmax were natural log-transformed prior to analysis and evaluated separately using a linear mixed effects model with a fixed effects term for treatment. An unstructured covariance matrix was used to allow for unequal treatment variances and to model the correlation between the treatment measurements within each subject. RESULTS: The PK of EE and LNG were not meaningfully altered by co-administration with MK-8591. For the comparison of (MK-8591 + LNG/EE) / (LNG/EE alone), the geometric mean ratios (GMRs) (90% confidence intervals (CIs)) for LNG AUC0-inf and Cmax were 1.13 (1.06, 1.20) and 0.965 (0.881, 1.06), respectively. For EE the GMRs (90% CI) for AUC0-inf and Cmax were 1.05 (0.981, 1.11) and 1.02 (0.971, 1.08), respectively. Co-administration of all three drugs was generally well tolerated. CONCLUSION: The results of this study support use of hormonal contraceptives in HIV-infected patients receiving MK-8591. DISCLOSURES: W. Ankrom, Merck & Co, Inc.: Employee and Shareholder, Salary. D. Jonathan, Merck: Employee, Salary. D. Rudd, Merck & Co., INC.: Employee, Salary. S. Zhang, Merck & Co, Inc.: Employee, Salary. K. Fillgrove, Merck & Co., Inc.: Employee, Salary. K. Gravesande, Kezia Gravesande: Research Contractor, Salary. R. Matthews, Merck: Employee, Salary. A. Stoch, Merck & Co, Inc.: Employee and Shareholder, Salary. M. Iwamoto, Merck & Co, Inc.: Employee and Shareholder, Salary. Oxford University Press 2018-11-26 /pmc/articles/PMC6255447/ http://dx.doi.org/10.1093/ofid/ofy210.559 Text en © The Author(s) 2018. Published by Oxford University Press on behalf of Infectious Diseases Society of America. http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs licence (http://creativecommons.org/licenses/by-nc-nd/4.0/), which permits non-commercial reproduction and distribution of the work, in any medium, provided the original work is not altered or transformed in any way, and that the work is properly cited. For commercial re-use, please contact journals.permissions@oup.com
spellingShingle Abstracts
Ankrom, Wendy
Jonathan, Daniel
Rudd, Deanne
Zhang, Sandra
Fillgrove, Kerry
Gravesande, Kezia
Matthews, Randolph
Brimhall, Darin
Stoch, Aubrey
Iwamoto, Marian
551. MK-8591 Does Not Alter the Pharmacokinetics of the Oral Contraceptives Ethinyl Estradiol and Levonorgestrel
title 551. MK-8591 Does Not Alter the Pharmacokinetics of the Oral Contraceptives Ethinyl Estradiol and Levonorgestrel
title_full 551. MK-8591 Does Not Alter the Pharmacokinetics of the Oral Contraceptives Ethinyl Estradiol and Levonorgestrel
title_fullStr 551. MK-8591 Does Not Alter the Pharmacokinetics of the Oral Contraceptives Ethinyl Estradiol and Levonorgestrel
title_full_unstemmed 551. MK-8591 Does Not Alter the Pharmacokinetics of the Oral Contraceptives Ethinyl Estradiol and Levonorgestrel
title_short 551. MK-8591 Does Not Alter the Pharmacokinetics of the Oral Contraceptives Ethinyl Estradiol and Levonorgestrel
title_sort 551. mk-8591 does not alter the pharmacokinetics of the oral contraceptives ethinyl estradiol and levonorgestrel
topic Abstracts
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6255447/
http://dx.doi.org/10.1093/ofid/ofy210.559
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