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Randomized, placebo-controlled trial of ADS-5102 (amantadine) extended-release capsules for levodopa-induced dyskinesia in Parkinson's disease (EASE LID 3).
Oertel, Wolfgang; Eggert, Karla; Pahwa, Rajesh; Tanner, Caroline M; Hauser, Robert A; Trenkwalder, Claudia; Ehret, Reinhard; Azulay, Jean Philippe; Isaacson, Stuart; Felt, Larissa; Stempien, Mary Jean.
Afiliação
  • Oertel W; Philipps University, Marburg, Germany.
  • Eggert K; Philipps University, Marburg, Germany.
  • Pahwa R; University of Kansas Medical Center, Kansas City, Kansas, USA.
  • Tanner CM; University of California San Francisco and San Francisco Veterans Affairs Medical Center, San Francisco, California, USA.
  • Hauser RA; University of South Florida, Tampa, Florida, USA.
  • Trenkwalder C; Paracelsus-Elena-Klinik, Kassel and Clinic Neurosurgery, University Medical Center, Goettingen, Germany.
  • Ehret R; Praxis Neurologie, Berlin, Germany.
  • Azulay JP; Hôpital de la Timone, Marseille, France.
  • Isaacson S; Parkinson's Disease and Movement Disorders Center, Boca Raton, Florida, USA.
  • Felt L; Adamas Pharmaceuticals, Inc., Emeryville, California, USA.
  • Stempien MJ; Adamas Pharmaceuticals, Inc., Emeryville, California, USA.
Mov Disord ; 32(12): 1701-1709, 2017 Dec.
Article em En | MEDLINE | ID: mdl-28833562
BACKGROUND: The treatment of levodopa-induced dyskinesia in Parkinson's disease (PD) is an unmet need with no approved drug therapy. OBJECTIVE: The purpose of this study was to investigate the efficacy and safety of 274 mg ADS-5102 (amantadine) extended-release capsules (equivalent to 340-mg amantadine HCl) for levodopa-induced dyskinesia in a randomized controlled trial. METHODS: PD patients with ≥1 hour of troublesome dyskinesia and at least mild functional impact were randomized to placebo or ADS-5102 once daily at bedtime for 13 weeks. The primary efficacy analysis was based on change from baseline to week 12 on the Unified Dyskinesia Rating Scale total score in the modified intent-to-treat population. OFF time was a key secondary measure. RESULTS: At week 12, least-squares mean change in the Unified Dyskinesia Rating Scale was -20.7 (standard error 2.2) for ADS-5102 (n = 37) and -6.3 (standard error 2.1) for placebo (n = 38; treatment difference -14.4, 95% confidence interval -20.4 to -8.3, P < .0001), indicating improvement in levodopa-induced dyskinesia. OFF time decreased 0.5 hours (standard error 0.3) for ADS-5102 from a baseline mean of 2.6 hours and increased 0.6 hours (standard error 0.3) for placebo from a baseline mean of 2.0 hours (treatment difference -1.1 hours, 95% confidence interval -2.0 to -0.2, P = .0199). The most common adverse events (ADS-5102 versus placebo) included dry mouth (13.5% versus 2.6%), nausea (13.5% versus 2.6%), decreased appetite (10.8% versus 0%), insomnia (10.8% versus 0%), orthostatic hypotension (10.8% versus 0%), constipation (8.1% versus 0%), falls (8.1% versus 5.3%), and visual hallucinations (8.1% versus 5.3%). Adverse events led to treatment discontinuation in 19% versus 8%, respectively. CONCLUSION: ADS-5102 274 mg is an oral pharmacotherapy demonstrating a significant decrease in levodopa-induced dyskinesia and improving OFF time. © 2017 The Authors. Movement Disorders published by Wiley Periodicals, Inc. on behalf of International Parkinson and Movement Disorder Society.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Amantadina / Preparações de Ação Retardada / Discinesia Induzida por Medicamentos / Antiparkinsonianos Tipo de estudo: Etiology_studies / Observational_studies Limite: Adult / Aged / Aged80 / Female / Humans / Male / Middle aged Idioma: En Ano de publicação: 2017 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Amantadina / Preparações de Ação Retardada / Discinesia Induzida por Medicamentos / Antiparkinsonianos Tipo de estudo: Etiology_studies / Observational_studies Limite: Adult / Aged / Aged80 / Female / Humans / Male / Middle aged Idioma: En Ano de publicação: 2017 Tipo de documento: Article