New and Emerging Medical Therapies in Parkinson's Disease.
Identifieur interne : 000000 ( PubMed/Curation ); suivant : 000001New and Emerging Medical Therapies in Parkinson's Disease.
Auteurs : Mitesh Lotia [États-Unis] ; Joseph JankovicSource :
- Expert opinion on pharmacotherapy ; 2016.
Abstract
Parkinson's disease (PD) is one of the most challenging neurodegenerative disorders to treat as it manifests with a large variety of troublesome, and often disabling, motor and non-motor symptoms. Despite limitations, such as motor and other complications, levodopa remains the most effective drug in the treatment of PD. Areas covered: In this review, we focus on phase 2 and 3 studies describing new and emerging medical therapies in PD. We discuss new formulations of levodopa, medications that prolong levodopa response and ameliorate levodopa-induced dyskinesias, and innovative delivery methods that are currently being evaluated in clinical trials or are in development with the promise of better efficacy and tolerability. We also describe novel non-dopaminergic drugs that have been identified for treatment of motor and non-motor symptoms. A specific section is designated for potential disease modifying therapies. Expert Opinion: Alternative formulations of levodopa appear to be promising especially to help with the motor fluctuations either by providing sustained benefits with controlled released formulations or ameliorate sudden OFF by formulations such as inhaled levodopa. Several different medications affecting non-dopaminergic pathways are being evaluated which may aide levodopa. As the understanding of the disease grows further, numerous novel neuroprotective or disease modifying therapies have been suggested. This along with development of medications to treat various non-motor symptoms will help improve quality of life of patients with PD.
DOI: 10.1517/14656566.2016.1149163
PubMed: 26830844
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<wicri:regionArea>a Fellow, Movement disorders, Parkinson's Disease Center and Movement Disorders Clinic , Department of Neurology Baylor College of Medicine , 7200 Cambridge St, Suite 9A, Houston , TX 77030-4202 , Tel: 713-798-9014 , Fax: 713-798-6808 </wicri:regionArea>
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<front><div type="abstract" xml:lang="en">Parkinson's disease (PD) is one of the most challenging neurodegenerative disorders to treat as it manifests with a large variety of troublesome, and often disabling, motor and non-motor symptoms. Despite limitations, such as motor and other complications, levodopa remains the most effective drug in the treatment of PD. Areas covered: In this review, we focus on phase 2 and 3 studies describing new and emerging medical therapies in PD. We discuss new formulations of levodopa, medications that prolong levodopa response and ameliorate levodopa-induced dyskinesias, and innovative delivery methods that are currently being evaluated in clinical trials or are in development with the promise of better efficacy and tolerability. We also describe novel non-dopaminergic drugs that have been identified for treatment of motor and non-motor symptoms. A specific section is designated for potential disease modifying therapies. Expert Opinion: Alternative formulations of levodopa appear to be promising especially to help with the motor fluctuations either by providing sustained benefits with controlled released formulations or ameliorate sudden OFF by formulations such as inhaled levodopa. Several different medications affecting non-dopaminergic pathways are being evaluated which may aide levodopa. As the understanding of the disease grows further, numerous novel neuroprotective or disease modifying therapies have been suggested. This along with development of medications to treat various non-motor symptoms will help improve quality of life of patients with PD.</div>
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<Abstract><AbstractText Label="INTRODUCTION" NlmCategory="BACKGROUND">Parkinson's disease (PD) is one of the most challenging neurodegenerative disorders to treat as it manifests with a large variety of troublesome, and often disabling, motor and non-motor symptoms. Despite limitations, such as motor and other complications, levodopa remains the most effective drug in the treatment of PD. Areas covered: In this review, we focus on phase 2 and 3 studies describing new and emerging medical therapies in PD. We discuss new formulations of levodopa, medications that prolong levodopa response and ameliorate levodopa-induced dyskinesias, and innovative delivery methods that are currently being evaluated in clinical trials or are in development with the promise of better efficacy and tolerability. We also describe novel non-dopaminergic drugs that have been identified for treatment of motor and non-motor symptoms. A specific section is designated for potential disease modifying therapies. Expert Opinion: Alternative formulations of levodopa appear to be promising especially to help with the motor fluctuations either by providing sustained benefits with controlled released formulations or ameliorate sudden OFF by formulations such as inhaled levodopa. Several different medications affecting non-dopaminergic pathways are being evaluated which may aide levodopa. As the understanding of the disease grows further, numerous novel neuroprotective or disease modifying therapies have been suggested. This along with development of medications to treat various non-motor symptoms will help improve quality of life of patients with PD.</AbstractText>
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<AffiliationInfo><Affiliation>a Fellow, Movement disorders, Parkinson's Disease Center and Movement Disorders Clinic , Department of Neurology Baylor College of Medicine , 7200 Cambridge St, Suite 9A, Houston , TX 77030-4202 , Tel: 713-798-9014 , Fax: 713-798-6808 , Email: mitesh.lotia@bcm.edu.</Affiliation>
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<AffiliationInfo><Affiliation>b Professor of Neurology, Distinguished Chair in Movement Disorders, Director, Parkinson's Disease Center and Movement Disorders Clinic, Department of Neurology , Baylor College of Medicine , 7200 Cambridge, Suite 9A, Houston , TX 77030-4202 , Tel: 713-798-5998 , Fax: 713-798-6808 , E-mail: josephj@bcm.edu , Web: www.jankovic.org.</Affiliation>
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