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The Clinical Development of Levodopa Inhalation Powder
Oral levodopa is the most effective treatment for Parkinson disease, but OFF periods emerge over time. Gastrointestinal dysfunction and food effects impact levodopa absorption, contributing to unpredictable control of OFF periods. Inhaled levodopa powder (Inbrija) is approved for on-demand treatment...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Lippincott Williams & Wilkins
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10010694/ https://www.ncbi.nlm.nih.gov/pubmed/36715241 http://dx.doi.org/10.1097/WNF.0000000000000540 |
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author | Hauser, Robert A. LeWitt, Peter A. Waters, Cheryl H. Grosset, Donald G. Blank, Burkhard |
author_facet | Hauser, Robert A. LeWitt, Peter A. Waters, Cheryl H. Grosset, Donald G. Blank, Burkhard |
author_sort | Hauser, Robert A. |
collection | PubMed |
description | Oral levodopa is the most effective treatment for Parkinson disease, but OFF periods emerge over time. Gastrointestinal dysfunction and food effects impact levodopa absorption, contributing to unpredictable control of OFF periods. Inhaled levodopa powder (Inbrija) is approved for on-demand treatment of OFF periods in patients receiving oral levodopa–dopa decarboxylase inhibitors. The 84-mg dose is administered via a breath-actuated inhaler. It provides pulmonary delivery of levodopa to the systemic circulation and is taken when a patient has an OFF period in between doses of regular oral levodopa medication. The pivotal SPAN-PD trial in patients experiencing OFF periods on oral dopaminergic therapy showed that levodopa inhalation powder 84 mg produced significant improvement in Unified Parkinson Disease Rating Scale Part III score, as measured 30 minutes postdose at week 12, and improvement was seen as early as 10 minutes. More patients in the levodopa inhalation powder group turned ON within 60 minutes of treatment and remained ON at 60 minutes than in the placebo group. Levodopa inhalation powder can also be used to treat early-morning OFF periods and, when used for up to 12 months, produced no clinically significant differences in pulmonary function compared with an untreated cohort. Levodopa inhalation powder 84 mg increased plasma levodopa concentration rapidly and with less variability than oral levodopa/carbidopa (25/100 mg). Most common adverse event associated with levodopa inhalation powder is cough, found in ~15% of patients in the SPAN-PD trial; otherwise, reported adverse events were consistent with those known to be associated with oral levodopa. |
format | Online Article Text |
id | pubmed-10010694 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Lippincott Williams & Wilkins |
record_format | MEDLINE/PubMed |
spelling | pubmed-100106942023-03-14 The Clinical Development of Levodopa Inhalation Powder Hauser, Robert A. LeWitt, Peter A. Waters, Cheryl H. Grosset, Donald G. Blank, Burkhard Clin Neuropharmacol Review Article Oral levodopa is the most effective treatment for Parkinson disease, but OFF periods emerge over time. Gastrointestinal dysfunction and food effects impact levodopa absorption, contributing to unpredictable control of OFF periods. Inhaled levodopa powder (Inbrija) is approved for on-demand treatment of OFF periods in patients receiving oral levodopa–dopa decarboxylase inhibitors. The 84-mg dose is administered via a breath-actuated inhaler. It provides pulmonary delivery of levodopa to the systemic circulation and is taken when a patient has an OFF period in between doses of regular oral levodopa medication. The pivotal SPAN-PD trial in patients experiencing OFF periods on oral dopaminergic therapy showed that levodopa inhalation powder 84 mg produced significant improvement in Unified Parkinson Disease Rating Scale Part III score, as measured 30 minutes postdose at week 12, and improvement was seen as early as 10 minutes. More patients in the levodopa inhalation powder group turned ON within 60 minutes of treatment and remained ON at 60 minutes than in the placebo group. Levodopa inhalation powder can also be used to treat early-morning OFF periods and, when used for up to 12 months, produced no clinically significant differences in pulmonary function compared with an untreated cohort. Levodopa inhalation powder 84 mg increased plasma levodopa concentration rapidly and with less variability than oral levodopa/carbidopa (25/100 mg). Most common adverse event associated with levodopa inhalation powder is cough, found in ~15% of patients in the SPAN-PD trial; otherwise, reported adverse events were consistent with those known to be associated with oral levodopa. Lippincott Williams & Wilkins 2023 2023-01-29 /pmc/articles/PMC10010694/ /pubmed/36715241 http://dx.doi.org/10.1097/WNF.0000000000000540 Text en Copyright © 2023 The Author(s). Published by Wolters Kluwer Health, Inc. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution-Non Commercial-No Derivatives License 4.0 (CCBY-NC-ND) (https://creativecommons.org/licenses/by-nc-nd/4.0/) , where it is permissible to download and share the work provided it is properly cited. The work cannot be changed in any way or used commercially without permission from the journal. |
spellingShingle | Review Article Hauser, Robert A. LeWitt, Peter A. Waters, Cheryl H. Grosset, Donald G. Blank, Burkhard The Clinical Development of Levodopa Inhalation Powder |
title | The Clinical Development of Levodopa Inhalation Powder |
title_full | The Clinical Development of Levodopa Inhalation Powder |
title_fullStr | The Clinical Development of Levodopa Inhalation Powder |
title_full_unstemmed | The Clinical Development of Levodopa Inhalation Powder |
title_short | The Clinical Development of Levodopa Inhalation Powder |
title_sort | clinical development of levodopa inhalation powder |
topic | Review Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10010694/ https://www.ncbi.nlm.nih.gov/pubmed/36715241 http://dx.doi.org/10.1097/WNF.0000000000000540 |
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