TY - JOUR
T1 - New dopaminergic therapies for PD motor complications
AU - Larson, Danielle
AU - Simuni, Tanya
N1 - Funding Information:
Danielle Larson, MD Relevant: none All COI: Has served as a consultant for Acadia Pharmaceuticals. Dr. Larson has received research funding from the Parkinson's Foundation and the Huntington's Disease Society of America.
Funding Information:
Tanya Simuni, MD has served as a consultant for Acadia, Caraway Therapeutics, Critical Path for Parkinson's Consortium (CPP), Denali, General Electric (GE), Neuroderm, Sanofi, Sinopia, Sunovion, Roche, Takeda, MJFF and Voyager. Dr. Simuni served on the ad board for Acadia, Denali, General Electric (GE), Sunovion, Roche. Dr. Simuni has served as a member of the scientific advisory board of Caraway Therapeutics, Neuroderm, Sanofi and UCB. Dr. Simuni has received research funding from Biogen, Roche, Neuroderm, Sanofi, Sun Pharma, Amneal, Prevail, UCB, NINDS, MJFF, Parkinson's Foundation.
Publisher Copyright:
© 2021 Elsevier Ltd
PY - 2022/2/15
Y1 - 2022/2/15
N2 - Background: Motor complications, characterized by “off” periods – when anti-parkinsonian medications are ineffective – and dyskinesia, are the hallmark of advanced Parkinson's disease (PD). While levodopa is the gold standard PD medication in terms of efficacy, its short duration of effect coupled with progressive loss of dopaminergic neurons leads to motor complications and fails to treat off periods. Purpose of review: This review focuses on novel dopaminergic therapies that were recently made clinically available or are currently in development for the treatment of motor complications. First, it will discuss rescue therapies for the treatment of off episodes, including novel apomorphine and levodopa formulations. Second, it will highlight adjunctive dopaminergic medications approved to reduce total daily off time. Third, it will discuss longer-acting levodopa formulations in development and introduce a novel selective dopamine agonist under study. Finally, it will cover novel dopaminergic delivery mechanisms, with specific focus on continuous subcutaneous infusions in development. The breadth of dopaminergic therapies recently approved or in development for motor complications, and specifically off time reduction, evokes cautious optimism. Gains in reducing off time with rescue therapies, adjunctive medications or longer-acting levodopa formulations are modest, and underscore the need for more continuous dopaminergic delivery to address the underlying pathophysiology and translate to clinically meaningful improvement in motor complications.
AB - Background: Motor complications, characterized by “off” periods – when anti-parkinsonian medications are ineffective – and dyskinesia, are the hallmark of advanced Parkinson's disease (PD). While levodopa is the gold standard PD medication in terms of efficacy, its short duration of effect coupled with progressive loss of dopaminergic neurons leads to motor complications and fails to treat off periods. Purpose of review: This review focuses on novel dopaminergic therapies that were recently made clinically available or are currently in development for the treatment of motor complications. First, it will discuss rescue therapies for the treatment of off episodes, including novel apomorphine and levodopa formulations. Second, it will highlight adjunctive dopaminergic medications approved to reduce total daily off time. Third, it will discuss longer-acting levodopa formulations in development and introduce a novel selective dopamine agonist under study. Finally, it will cover novel dopaminergic delivery mechanisms, with specific focus on continuous subcutaneous infusions in development. The breadth of dopaminergic therapies recently approved or in development for motor complications, and specifically off time reduction, evokes cautious optimism. Gains in reducing off time with rescue therapies, adjunctive medications or longer-acting levodopa formulations are modest, and underscore the need for more continuous dopaminergic delivery to address the underlying pathophysiology and translate to clinically meaningful improvement in motor complications.
KW - Dopaminergic therapy
KW - Infusions
KW - Parkinson's disease
KW - Rescue therapy
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U2 - 10.1016/j.neuropharm.2021.108869
DO - 10.1016/j.neuropharm.2021.108869
M3 - Review article
C2 - 34742740
AN - SCOPUS:85119618468
SN - 0028-3908
VL - 204
JO - Neuropharmacology
JF - Neuropharmacology
M1 - 108869
ER -