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Orally inhaled levodopa (CVT-301) for early morning OFF periods in Parkinson's disease.
Hauser, Robert A; Isaacson, Stuart H; Ellenbogen, Aaron; Safirstein, Beth E; Truong, Daniel D; Komjathy, Steven F; Kegler-Ebo, Deena M; Zhao, Ping; Oh, Charles.
Afiliação
  • Hauser RA; University of South Florida, Tampa, FL, USA. Electronic address: rhauser@health.usf.edu.
  • Isaacson SH; Parkinson's Disease and Movement Disorders Center of Boca Raton, Boca Raton, FL, USA.
  • Ellenbogen A; Quest Research Institute, Bingham Farms, MI, USA.
  • Safirstein BE; MD Clinical, Hallandale Beach, FL, USA.
  • Truong DD; The Truong Neuroscience Institute, Orange Coast Memorial Medical Center, Fountain Valley, CA, USA; Department of Psychiatry and Neuroscience, University of California Riverside, Riverside, CA, USA.
  • Komjathy SF; Acorda Therapeutics, Inc., Ardsley, NY, USA.
  • Kegler-Ebo DM; Acorda Therapeutics, Inc., Ardsley, NY, USA.
  • Zhao P; Acorda Therapeutics, Inc., Ardsley, NY, USA.
  • Oh C; Acorda Therapeutics, Inc., Ardsley, NY, USA.
Parkinsonism Relat Disord ; 64: 175-180, 2019 07.
Article em En | MEDLINE | ID: mdl-30992235
ABSTRACT

BACKGROUND:

CVT-301 (Inbrija) is a self-administered orally inhaled levodopa approved for the intermittent treatment of OFF episodes in patients with Parkinson's disease (PD) treated with carbidopa/levodopa. Prior studies only evaluated CVT-301 after the first ON of the day. OBJECTIVE AND

METHODS:

The objective of this study was to evaluate the safety and tolerability of CVT-301 for early morning OFF. Using a randomized, double-blind, 2-way crossover design, eligible patients in the morning OFF state (having not received PD medication overnight) received a single dose of CVT-301 84 mg or placebo on 2 dosing days, immediately after their first morning oral carbidopa/levodopa dose. Safety assessments included treatment-emergent adverse events, vital signs, and patient- and examiner-reported dyskinesia. An exploratory efficacy assessment was examiner-rated time-to-ON with carbidopa/levodopa + CVT-301 vs carbidopa/levodopa + placebo.

RESULTS:

Of the 36 patients (mean age 62.9 years) who enrolled and completed the study, 9 (25.0%) reported treatment-emergent adverse events following CVT-301 administration; 4 (11.1%) reported treatment-emergent adverse events following placebo. The most common adverse event was cough (4 [11.1%] for CVT-301 vs 1 [2.8%] for placebo), which was typically mild and transient. Incidence of asymptomatic orthostatic hypotension (CVT-301, 6; placebo, 7) and examiner-rated dyskinesia were similar for both (36-39% mild, 3-6% moderate, and 0% severe). Median time-to-ON was 25.0 min following carbidopa/levodopa + CVT-301 and 35.5 min following carbidopa/levodopa + placebo (P = 0.26). At 30 min, more patients had turned ON following carbidopa/levodopa + CVT-301 administration (66.7%), compared with carbidopa/levodopa + placebo (44.5%) (P = 0.040).

CONCLUSION:

Single doses of CVT-301 84 mg administered with oral carbidopa/levodopa for early morning OFF symptoms were well-tolerated, with no notable safety concerns.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Doença de Parkinson / Levodopa / Antiparkinsonianos Tipo de estudo: Clinical_trials Limite: Aged / Female / Humans / Male / Middle aged Idioma: En Revista: Parkinsonism Relat Disord Ano de publicação: 2019 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Doença de Parkinson / Levodopa / Antiparkinsonianos Tipo de estudo: Clinical_trials Limite: Aged / Female / Humans / Male / Middle aged Idioma: En Revista: Parkinsonism Relat Disord Ano de publicação: 2019 Tipo de documento: Article