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Extended regimen of a levonorgestrel/ethinyl estradiol transdermal delivery system: Predicted serum hormone levels using a population pharmacokinetic model
OBJECTIVE: This study employed population pharmacokinetic (popPK) models to predict levonorgestrel (LNG) and ethinyl estradiol (EE) exposure after dosing with the transdermal contraceptive TWIRLA(®) (LNG/EE TDS) as a 12-week extended regimen in a healthy female population. METHODS: PopPK models were...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9794042/ https://www.ncbi.nlm.nih.gov/pubmed/36574387 http://dx.doi.org/10.1371/journal.pone.0279640 |
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author | Stanczyk, Frank Z. Archer, David F. Lohmer, Lauren R. L. Pirone, Jason Previtera, Michelle Korner, Paul |
author_facet | Stanczyk, Frank Z. Archer, David F. Lohmer, Lauren R. L. Pirone, Jason Previtera, Michelle Korner, Paul |
author_sort | Stanczyk, Frank Z. |
collection | PubMed |
description | OBJECTIVE: This study employed population pharmacokinetic (popPK) models to predict levonorgestrel (LNG) and ethinyl estradiol (EE) exposure after dosing with the transdermal contraceptive TWIRLA(®) (LNG/EE TDS) as a 12-week extended regimen in a healthy female population. METHODS: PopPK models were developed using data from a previously published phase 1, open-label, randomized clinical trial, ATI-CL14 (NCT01243580), in 36 healthy individuals. Models used cycle 2 data from 18 individuals who received the LNG/EE TDS, delivering LNG 120 μg/day and EE 30 μg/day, followed by a 1-week TDS-free period. Noncompartmental PK analyses were performed on simulated concentration–time profiles of 12 consecutive weeks of LNG/EE TDS use. RESULTS: The simulated concentration–time profiles and PK parameters for the simulated extended regimen indicated that predicted LNG and EE exposures at week 12 were similar to week 3 (predicted geometric mean EE area under the concentration-time curve from time 0 to 168 h [AUC(0-168)] on week 3 was 0.2% lower than week 12 and LNG AUC(0-168) on week 3 was 0.9% lower than week 12), suggesting both were at steady state by week 3. Therefore, no notable accumulation beyond that at week 3 is predicted for LNG and EE following a 12-week extended regimen. The results are supported by the accumulation ratios based on maximum concentration and the area under the curve being similar at weeks 3 and 12 for LNG and EE. CONCLUSION: These results indicate that a 12-week extended LNG/EE regimen would provide similar systemic hormonal exposure as that seen by week 3 in a standard 28-day regimen, without further hormonal accumulation. The data support the safe use of a non-daily, low-dose hormonal contraceptive in an extended regimen but should be confirmed in a clinical PK study. |
format | Online Article Text |
id | pubmed-9794042 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-97940422022-12-28 Extended regimen of a levonorgestrel/ethinyl estradiol transdermal delivery system: Predicted serum hormone levels using a population pharmacokinetic model Stanczyk, Frank Z. Archer, David F. Lohmer, Lauren R. L. Pirone, Jason Previtera, Michelle Korner, Paul PLoS One Research Article OBJECTIVE: This study employed population pharmacokinetic (popPK) models to predict levonorgestrel (LNG) and ethinyl estradiol (EE) exposure after dosing with the transdermal contraceptive TWIRLA(®) (LNG/EE TDS) as a 12-week extended regimen in a healthy female population. METHODS: PopPK models were developed using data from a previously published phase 1, open-label, randomized clinical trial, ATI-CL14 (NCT01243580), in 36 healthy individuals. Models used cycle 2 data from 18 individuals who received the LNG/EE TDS, delivering LNG 120 μg/day and EE 30 μg/day, followed by a 1-week TDS-free period. Noncompartmental PK analyses were performed on simulated concentration–time profiles of 12 consecutive weeks of LNG/EE TDS use. RESULTS: The simulated concentration–time profiles and PK parameters for the simulated extended regimen indicated that predicted LNG and EE exposures at week 12 were similar to week 3 (predicted geometric mean EE area under the concentration-time curve from time 0 to 168 h [AUC(0-168)] on week 3 was 0.2% lower than week 12 and LNG AUC(0-168) on week 3 was 0.9% lower than week 12), suggesting both were at steady state by week 3. Therefore, no notable accumulation beyond that at week 3 is predicted for LNG and EE following a 12-week extended regimen. The results are supported by the accumulation ratios based on maximum concentration and the area under the curve being similar at weeks 3 and 12 for LNG and EE. CONCLUSION: These results indicate that a 12-week extended LNG/EE regimen would provide similar systemic hormonal exposure as that seen by week 3 in a standard 28-day regimen, without further hormonal accumulation. The data support the safe use of a non-daily, low-dose hormonal contraceptive in an extended regimen but should be confirmed in a clinical PK study. Public Library of Science 2022-12-27 /pmc/articles/PMC9794042/ /pubmed/36574387 http://dx.doi.org/10.1371/journal.pone.0279640 Text en © 2022 Stanczyk et al https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Article Stanczyk, Frank Z. Archer, David F. Lohmer, Lauren R. L. Pirone, Jason Previtera, Michelle Korner, Paul Extended regimen of a levonorgestrel/ethinyl estradiol transdermal delivery system: Predicted serum hormone levels using a population pharmacokinetic model |
title | Extended regimen of a levonorgestrel/ethinyl estradiol transdermal delivery system: Predicted serum hormone levels using a population pharmacokinetic model |
title_full | Extended regimen of a levonorgestrel/ethinyl estradiol transdermal delivery system: Predicted serum hormone levels using a population pharmacokinetic model |
title_fullStr | Extended regimen of a levonorgestrel/ethinyl estradiol transdermal delivery system: Predicted serum hormone levels using a population pharmacokinetic model |
title_full_unstemmed | Extended regimen of a levonorgestrel/ethinyl estradiol transdermal delivery system: Predicted serum hormone levels using a population pharmacokinetic model |
title_short | Extended regimen of a levonorgestrel/ethinyl estradiol transdermal delivery system: Predicted serum hormone levels using a population pharmacokinetic model |
title_sort | extended regimen of a levonorgestrel/ethinyl estradiol transdermal delivery system: predicted serum hormone levels using a population pharmacokinetic model |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9794042/ https://www.ncbi.nlm.nih.gov/pubmed/36574387 http://dx.doi.org/10.1371/journal.pone.0279640 |
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