Efficacy of Istradefylline, an Adenosine A2A Receptor Antagonist, as Adjunctive Therapy to Levodopa in Parkinson's Disease: A Pooled Analysis of 8 Phase 2b/3 Trials

التفاصيل البيبلوغرافية
العنوان: Efficacy of Istradefylline, an Adenosine A2A Receptor Antagonist, as Adjunctive Therapy to Levodopa in Parkinson's Disease: A Pooled Analysis of 8 Phase 2b/3 Trials
المؤلفون: Stuart Isaacson, Fabrizio Stocchi, Yu Nakajima, Hideki Mochizuki, Peter A LeWitt, June Li, Nobutaka Hattori, Hubert H. Fernandez, Robert Ristuccia, Olivier Rascol, Robert A. Hauser, Akihisa Mori
المصدر: Journal of Parkinson's Disease
سنة النشر: 2021
مصطلحات موضوعية: Research Report, istradefylline, Levodopa, Receptor, Adenosine A2A, Adenosine 2A receptor antagonist, Decarboxylase inhibitor, Placebo, Antiparkinson Agents, Cellular and Molecular Neuroscience, chemistry.chemical_compound, Double-Blind Method, medicine, Clinical endpoint, Humans, Randomized Controlled Trials as Topic, Benserazide, Dyskinesias, treatment, business.industry, Parkinson Disease, Istradefylline, Adenosine A2 Receptor Antagonists, Treatment Outcome, Dyskinesia, chemistry, Purinergic P1 Receptor Antagonists, Purines, Anesthesia, Carbidopa, Parkinson’s disease, Neurology (clinical), medicine.symptom, business, medicine.drug
الوصف: Background: Istradefylline is a selective adenosine A2A receptor antagonist for the treatment of patients with Parkinson’s disease (PD) experiencing OFF episodes while on levodopa/decarboxylase inhibitor. Objective: This pooled analysis of eight randomized, placebo-controlled, double-blind phase 2b/3 studies evaluated the efficacy and safety of istradefylline. Methods: Istradefylline was evaluated in PD patients receiving levodopa with carbidopa/benserazide and experiencing motor fluctuations. Eight 12- or 16-week trials were conducted (n = 3,245); four of these studies were the basis for istradefylline’s FDA approval. Change in OFF time as assessed in patient-completed 24-h PD diaries at Week 12 was the primary endpoint. All studies were designed with common methodology, thereby permitting pooling of data. Pooled analysis results from once-daily oral istradefylline (20 and 40 mg/day) and placebo were evaluated using a mixed-model repeated-measures approach including study as a factor. Results: Among 2,719 patients (placebo, n = 992; 20 mg/day, n = 848; 40 mg/day, n = 879), OFF hours/day were reduced at Week 12 at istradefylline dosages of 20 mg/day (least-squares mean difference [LSMD] from placebo in reduction from baseline [95%CI], –0.38 h [–0.61, –0.15]) and 40 mg/day (–0.45 h [–0.68, –0.22], p
تدمد: 1877-718X
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::88ddf0eaaee9074f562ab1a7dac0418f
https://pubmed.ncbi.nlm.nih.gov/34486986
حقوق: OPEN
رقم الأكسشن: edsair.doi.dedup.....88ddf0eaaee9074f562ab1a7dac0418f
قاعدة البيانات: OpenAIRE