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Pharmacokinetics of Coadministered Viloxazine Extended-Release (SPN-812) and Methylphenidate in Healthy Adults
BACKGROUND AND OBJECTIVES: Viloxazine extended-release (viloxazine ER, SPN-812) is a novel non-stimulant with activity at serotonin receptors and the norepinephrine transporter, which is under investigation as a potential treatment for attention-deficit/hyperactivity disorder. Given the potential fo...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Springer International Publishing
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7886742/ https://www.ncbi.nlm.nih.gov/pubmed/33368026 http://dx.doi.org/10.1007/s40261-020-00992-6 |
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author | Faison, Shamia L. Fry, Nicholas Adewole, Toyin Odebo, Oyinkansola Schwabe, Stefan Wang, Zhao Maletic, Vladimir Nasser, Azmi |
author_facet | Faison, Shamia L. Fry, Nicholas Adewole, Toyin Odebo, Oyinkansola Schwabe, Stefan Wang, Zhao Maletic, Vladimir Nasser, Azmi |
author_sort | Faison, Shamia L. |
collection | PubMed |
description | BACKGROUND AND OBJECTIVES: Viloxazine extended-release (viloxazine ER, SPN-812) is a novel non-stimulant with activity at serotonin receptors and the norepinephrine transporter, which is under investigation as a potential treatment for attention-deficit/hyperactivity disorder. Given the potential for viloxazine ER to be coadministered with other pharmacotherapies, this trial investigated the pharmacokinetics and safety of combination viloxazine ER + methylphenidate versus viloxazine ER or methylphenidate alone. METHODS: In this single-center, crossover, open-label trial, healthy adult participants received oral administration of 700 mg viloxazine ER alone, 36 mg methylphenidate alone, and combination viloxazine ER (700 mg) + methylphenidate (36 mg), with blood samples collected over 4 days post-administration. The active drug in viloxazine ER (viloxazine) and methylphenidate was measured using chromatographic tandem mass spectrometry. Safety assessments included adverse events (AEs), vital signs, echocardiograms, and clinical laboratory evaluations. RESULTS: Of 36 healthy adults who were enrolled, 34 completed the trial. The geometric least squares mean ratios are reported as [combination/single drug (90% confidence intervals)]. For viloxazine ER, maximum measured plasma concentration (C(max)) = 100.98% (96.21–105.99), area under the concentration–time curve from time zero to the last measurable time (AUC(t)) = 98.62% (96.21–101.08), and area under the concentration–time curve from time zero to infinity (AUC(∞)) = 98.96% (96.55–101.44). For methylphenidate, C(max) = 103.55% (97.42–110.07), AUC(t) = 106.67% (101.01–112.64), and AUC(∞) = 106.61% (100.99–112.54). All reported AEs were mild in severity. CONCLUSIONS: Coadministration of viloxazine ER and methylphenidate did not impact the pharmacokinetics of viloxazine or methylphenidate relative to administration of either drug alone. The combination appeared to be safe and well tolerated. |
format | Online Article Text |
id | pubmed-7886742 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Springer International Publishing |
record_format | MEDLINE/PubMed |
spelling | pubmed-78867422021-03-03 Pharmacokinetics of Coadministered Viloxazine Extended-Release (SPN-812) and Methylphenidate in Healthy Adults Faison, Shamia L. Fry, Nicholas Adewole, Toyin Odebo, Oyinkansola Schwabe, Stefan Wang, Zhao Maletic, Vladimir Nasser, Azmi Clin Drug Investig Original Research Article BACKGROUND AND OBJECTIVES: Viloxazine extended-release (viloxazine ER, SPN-812) is a novel non-stimulant with activity at serotonin receptors and the norepinephrine transporter, which is under investigation as a potential treatment for attention-deficit/hyperactivity disorder. Given the potential for viloxazine ER to be coadministered with other pharmacotherapies, this trial investigated the pharmacokinetics and safety of combination viloxazine ER + methylphenidate versus viloxazine ER or methylphenidate alone. METHODS: In this single-center, crossover, open-label trial, healthy adult participants received oral administration of 700 mg viloxazine ER alone, 36 mg methylphenidate alone, and combination viloxazine ER (700 mg) + methylphenidate (36 mg), with blood samples collected over 4 days post-administration. The active drug in viloxazine ER (viloxazine) and methylphenidate was measured using chromatographic tandem mass spectrometry. Safety assessments included adverse events (AEs), vital signs, echocardiograms, and clinical laboratory evaluations. RESULTS: Of 36 healthy adults who were enrolled, 34 completed the trial. The geometric least squares mean ratios are reported as [combination/single drug (90% confidence intervals)]. For viloxazine ER, maximum measured plasma concentration (C(max)) = 100.98% (96.21–105.99), area under the concentration–time curve from time zero to the last measurable time (AUC(t)) = 98.62% (96.21–101.08), and area under the concentration–time curve from time zero to infinity (AUC(∞)) = 98.96% (96.55–101.44). For methylphenidate, C(max) = 103.55% (97.42–110.07), AUC(t) = 106.67% (101.01–112.64), and AUC(∞) = 106.61% (100.99–112.54). All reported AEs were mild in severity. CONCLUSIONS: Coadministration of viloxazine ER and methylphenidate did not impact the pharmacokinetics of viloxazine or methylphenidate relative to administration of either drug alone. The combination appeared to be safe and well tolerated. Springer International Publishing 2020-12-23 2021 /pmc/articles/PMC7886742/ /pubmed/33368026 http://dx.doi.org/10.1007/s40261-020-00992-6 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 Faison, Shamia L. Fry, Nicholas Adewole, Toyin Odebo, Oyinkansola Schwabe, Stefan Wang, Zhao Maletic, Vladimir Nasser, Azmi Pharmacokinetics of Coadministered Viloxazine Extended-Release (SPN-812) and Methylphenidate in Healthy Adults |
title | Pharmacokinetics of Coadministered Viloxazine Extended-Release (SPN-812) and Methylphenidate in Healthy Adults |
title_full | Pharmacokinetics of Coadministered Viloxazine Extended-Release (SPN-812) and Methylphenidate in Healthy Adults |
title_fullStr | Pharmacokinetics of Coadministered Viloxazine Extended-Release (SPN-812) and Methylphenidate in Healthy Adults |
title_full_unstemmed | Pharmacokinetics of Coadministered Viloxazine Extended-Release (SPN-812) and Methylphenidate in Healthy Adults |
title_short | Pharmacokinetics of Coadministered Viloxazine Extended-Release (SPN-812) and Methylphenidate in Healthy Adults |
title_sort | pharmacokinetics of coadministered viloxazine extended-release (spn-812) and methylphenidate in healthy adults |
topic | Original Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7886742/ https://www.ncbi.nlm.nih.gov/pubmed/33368026 http://dx.doi.org/10.1007/s40261-020-00992-6 |
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