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Levodopa-Carbidopa Intestinal Gel Pharmacokinetics: Lower Variability than Oral Levodopa-Carbidopa

In a double-blind, double-dummy, double-titration Phase 3 trial in advanced Parkinson’s disease (PD) patients, the efficacy and safety of Levodopa-carbidopa intestinal gel (LCIG) infusion were characterized relative to immediate-release oral levodopa-carbidopa (LC-oral) treatment. We present in this...

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Autores principales: Othman, Ahmed A., Rosebraugh, Matthew, Chatamra, Krai, Locke, Charles, Dutta, Sandeep
Formato: Online Artículo Texto
Lenguaje:English
Publicado: IOS Press 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5438475/
https://www.ncbi.nlm.nih.gov/pubmed/28211816
http://dx.doi.org/10.3233/JPD-161042
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author Othman, Ahmed A.
Rosebraugh, Matthew
Chatamra, Krai
Locke, Charles
Dutta, Sandeep
author_facet Othman, Ahmed A.
Rosebraugh, Matthew
Chatamra, Krai
Locke, Charles
Dutta, Sandeep
author_sort Othman, Ahmed A.
collection PubMed
description In a double-blind, double-dummy, double-titration Phase 3 trial in advanced Parkinson’s disease (PD) patients, the efficacy and safety of Levodopa-carbidopa intestinal gel (LCIG) infusion were characterized relative to immediate-release oral levodopa-carbidopa (LC-oral) treatment. We present in this report the comparative pharmacokinetic profiles of LCIG and LC-oral from this pivotal study. The results presented in this report clearly demonstrate that LCIG results in lower variability and fluctuations in levodopa and carbidopa plasma concentrations compared to LC-oral. The superior pharmacokinetic profiles with LCIG were consistent with its improved efficacy compared to LC-oral as demonstrated in this study.
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spelling pubmed-54384752017-05-30 Levodopa-Carbidopa Intestinal Gel Pharmacokinetics: Lower Variability than Oral Levodopa-Carbidopa Othman, Ahmed A. Rosebraugh, Matthew Chatamra, Krai Locke, Charles Dutta, Sandeep J Parkinsons Dis Short Communication In a double-blind, double-dummy, double-titration Phase 3 trial in advanced Parkinson’s disease (PD) patients, the efficacy and safety of Levodopa-carbidopa intestinal gel (LCIG) infusion were characterized relative to immediate-release oral levodopa-carbidopa (LC-oral) treatment. We present in this report the comparative pharmacokinetic profiles of LCIG and LC-oral from this pivotal study. The results presented in this report clearly demonstrate that LCIG results in lower variability and fluctuations in levodopa and carbidopa plasma concentrations compared to LC-oral. The superior pharmacokinetic profiles with LCIG were consistent with its improved efficacy compared to LC-oral as demonstrated in this study. IOS Press 2017-05-16 /pmc/articles/PMC5438475/ /pubmed/28211816 http://dx.doi.org/10.3233/JPD-161042 Text en IOS Press and the authors. All rights reserved https://creativecommons.org/licenses/by-nc/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution Non-Commercial (CC BY-NC 4.0) License (https://creativecommons.org/licenses/by-nc/4.0/) , which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Short Communication
Othman, Ahmed A.
Rosebraugh, Matthew
Chatamra, Krai
Locke, Charles
Dutta, Sandeep
Levodopa-Carbidopa Intestinal Gel Pharmacokinetics: Lower Variability than Oral Levodopa-Carbidopa
title Levodopa-Carbidopa Intestinal Gel Pharmacokinetics: Lower Variability than Oral Levodopa-Carbidopa
title_full Levodopa-Carbidopa Intestinal Gel Pharmacokinetics: Lower Variability than Oral Levodopa-Carbidopa
title_fullStr Levodopa-Carbidopa Intestinal Gel Pharmacokinetics: Lower Variability than Oral Levodopa-Carbidopa
title_full_unstemmed Levodopa-Carbidopa Intestinal Gel Pharmacokinetics: Lower Variability than Oral Levodopa-Carbidopa
title_short Levodopa-Carbidopa Intestinal Gel Pharmacokinetics: Lower Variability than Oral Levodopa-Carbidopa
title_sort levodopa-carbidopa intestinal gel pharmacokinetics: lower variability than oral levodopa-carbidopa
topic Short Communication
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5438475/
https://www.ncbi.nlm.nih.gov/pubmed/28211816
http://dx.doi.org/10.3233/JPD-161042
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