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Istradefylline, a novel adenosine A2A receptor antagonist, for the treatment of Parkinson's disease.

Abstract
Dopamine replacement therapy effectively treats the early motor symptoms of Parkinson's disease (PD). However, its association with the development of motor complications limits its usefulness in late stages of the disease. Adenosine A(2A) receptors are localised to the indirect striatal output function and control motor behaviour. They are active in predictive experimental models of PD and appear to be promising as the first major non-dopaminergic therapy for PD. Istradefylline is a novel adenosine A(2A) receptor antagonist currently in Phase III clinical trials for efficacy in patients with PD; results from Phase II clinical trials demonstrated that it provides a clinically meaningful reduction in 'off' time and an increased 'on' time with non-troublesome dyskinesia in levodopa-treated patients with established motor complications, and is safe and well tolerated.
AuthorsPeter Jenner
JournalExpert opinion on investigational drugs (Expert Opin Investig Drugs) Vol. 14 Issue 6 Pg. 729-38 (Jun 2005) ISSN: 1744-7658 [Electronic] England
PMID16004599 (Publication Type: Journal Article, Review)
Chemical References
  • Adenosine A2 Receptor Antagonists
  • Antiparkinson Agents
  • Drugs, Investigational
  • Purines
  • Receptor, Adenosine A2A
  • istradefylline
Topics
  • Adenosine A2 Receptor Antagonists
  • Animals
  • Antiparkinson Agents (chemistry, pharmacology, therapeutic use)
  • Clinical Trials as Topic (statistics & numerical data, trends)
  • Drugs, Investigational (chemistry, pharmacology, therapeutic use)
  • Humans
  • Parkinson Disease (drug therapy, metabolism)
  • Purines (chemistry, pharmacology, therapeutic use)
  • Receptor, Adenosine A2A (metabolism)

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