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Evaluation of the Potential Pharmacokinetic Interactions Between Vixotrigine and an Oral Contraceptive

BACKGROUND AND OBJECTIVE: Vixotrigine is a voltage- and use-dependent sodium channel blocker in development for neuropathic pain management. This study evaluated the effect of coadministration of vixotrigine (metabolized primarily via uridine diphosphate-glucuronosyltransferases) and an oral contrac...

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Autores principales: Zhao, Yuan, Versavel, Mark, Tidemann-Miller, Beth, Christmann, Romy, Naik, Himanshu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer International Publishing 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7359159/
https://www.ncbi.nlm.nih.gov/pubmed/32564301
http://dx.doi.org/10.1007/s40261-020-00931-5
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author Zhao, Yuan
Versavel, Mark
Tidemann-Miller, Beth
Christmann, Romy
Naik, Himanshu
author_facet Zhao, Yuan
Versavel, Mark
Tidemann-Miller, Beth
Christmann, Romy
Naik, Himanshu
author_sort Zhao, Yuan
collection PubMed
description BACKGROUND AND OBJECTIVE: Vixotrigine is a voltage- and use-dependent sodium channel blocker in development for neuropathic pain management. This study evaluated the effect of coadministration of vixotrigine (metabolized primarily via uridine diphosphate-glucuronosyltransferases) and an oral contraceptive containing ethinyl estradiol (uridine diphosphate-glucuronosyltransferase inducer) and levonorgestrel on the pharmacokinetics and safety of all three compounds. METHODS: In this phase I, open-label, fixed-sequence, multiple-dose study, 36 healthy women received oral vixotrigine 150 mg three times daily for 6 days and once on day 7. This was followed by a washout period, days 8–11. The oral contraceptive was administered alone on days 12–25 and with vixotrigine 150 mg three times daily on days 26–32. Serial blood samples were collected for pharmacokinetic analysis. Safety was assessed. RESULTS: The geometric least-squares mean ratios (90% confidence intervals) for the area under the concentration-time curve over 8 h and maximum concentration of vixotrigine co-administered with an oral contraceptive vs vixotrigine alone were 0.85 (0.82–0.89) and 0.91 (0.87–0.96), respectively. The geometric least-squares mean ratios (90% confidence interval) for area under the concentration-time curve over 24 h and maximum concentration of ethinyl estradiol with vixotrigine vs ethinyl estradiol alone were 0.94 (0.91–0.97) and 0.89 (0.84–0.94), respectively; the ratios for levonorgestrel with vixotrigine vs levonorgestrel alone were 1.06 (0.98–1.16) and 1.05 (0.98–1.13), respectively. No adverse events occurring with vixotrigine alone were deemed related to the study drug by the investigators. CONCLUSIONS: Coadministration of vixotrigine and an oral contraceptive containing ethinyl estradiol and levonorgestrel had no clinically relevant effect on exposure of all three compounds. TRIAL REGISTRATION: ClinicalTrials.gov registration number: NCT03324685 (registered 25 October, 2017).
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spelling pubmed-73591592020-07-16 Evaluation of the Potential Pharmacokinetic Interactions Between Vixotrigine and an Oral Contraceptive Zhao, Yuan Versavel, Mark Tidemann-Miller, Beth Christmann, Romy Naik, Himanshu Clin Drug Investig Original Research Article BACKGROUND AND OBJECTIVE: Vixotrigine is a voltage- and use-dependent sodium channel blocker in development for neuropathic pain management. This study evaluated the effect of coadministration of vixotrigine (metabolized primarily via uridine diphosphate-glucuronosyltransferases) and an oral contraceptive containing ethinyl estradiol (uridine diphosphate-glucuronosyltransferase inducer) and levonorgestrel on the pharmacokinetics and safety of all three compounds. METHODS: In this phase I, open-label, fixed-sequence, multiple-dose study, 36 healthy women received oral vixotrigine 150 mg three times daily for 6 days and once on day 7. This was followed by a washout period, days 8–11. The oral contraceptive was administered alone on days 12–25 and with vixotrigine 150 mg three times daily on days 26–32. Serial blood samples were collected for pharmacokinetic analysis. Safety was assessed. RESULTS: The geometric least-squares mean ratios (90% confidence intervals) for the area under the concentration-time curve over 8 h and maximum concentration of vixotrigine co-administered with an oral contraceptive vs vixotrigine alone were 0.85 (0.82–0.89) and 0.91 (0.87–0.96), respectively. The geometric least-squares mean ratios (90% confidence interval) for area under the concentration-time curve over 24 h and maximum concentration of ethinyl estradiol with vixotrigine vs ethinyl estradiol alone were 0.94 (0.91–0.97) and 0.89 (0.84–0.94), respectively; the ratios for levonorgestrel with vixotrigine vs levonorgestrel alone were 1.06 (0.98–1.16) and 1.05 (0.98–1.13), respectively. No adverse events occurring with vixotrigine alone were deemed related to the study drug by the investigators. CONCLUSIONS: Coadministration of vixotrigine and an oral contraceptive containing ethinyl estradiol and levonorgestrel had no clinically relevant effect on exposure of all three compounds. TRIAL REGISTRATION: ClinicalTrials.gov registration number: NCT03324685 (registered 25 October, 2017). Springer International Publishing 2020-06-20 2020 /pmc/articles/PMC7359159/ /pubmed/32564301 http://dx.doi.org/10.1007/s40261-020-00931-5 Text en © The Author(s) 2020 Open AccessThis article is licensed under a Creative Commons Attribution-NonCommercial 4.0 International License, which permits any non-commercial use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by-nc/4.0/.
spellingShingle Original Research Article
Zhao, Yuan
Versavel, Mark
Tidemann-Miller, Beth
Christmann, Romy
Naik, Himanshu
Evaluation of the Potential Pharmacokinetic Interactions Between Vixotrigine and an Oral Contraceptive
title Evaluation of the Potential Pharmacokinetic Interactions Between Vixotrigine and an Oral Contraceptive
title_full Evaluation of the Potential Pharmacokinetic Interactions Between Vixotrigine and an Oral Contraceptive
title_fullStr Evaluation of the Potential Pharmacokinetic Interactions Between Vixotrigine and an Oral Contraceptive
title_full_unstemmed Evaluation of the Potential Pharmacokinetic Interactions Between Vixotrigine and an Oral Contraceptive
title_short Evaluation of the Potential Pharmacokinetic Interactions Between Vixotrigine and an Oral Contraceptive
title_sort evaluation of the potential pharmacokinetic interactions between vixotrigine and an oral contraceptive
topic Original Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7359159/
https://www.ncbi.nlm.nih.gov/pubmed/32564301
http://dx.doi.org/10.1007/s40261-020-00931-5
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