Adenosine A2A receptor antagonist istradefylline reduces daily OFF time in Parkinson's disease

Mov Disord. 2013 Jul;28(8):1138-41. doi: 10.1002/mds.25418. Epub 2013 Mar 11.

Abstract

Background: We evaluated the efficacy and safety of istradefylline, a selective adenosine A2A receptor antagonist administered as adjunctive treatment to levodopa for 12 weeks in a double-blind manner in Parkinson's disease patients with motor complications in Japan.

Methods: A total of 373 subjects were randomized to receive placebo (n=126), istradefylline 20 mg/day (n=123), or istradefylline 40 mg/day (n=124). The primary efficacy variable was the change in daily OFF time. Other secondary variables were also evaluated.

Results: The change in daily OFF time was significantly reduced in the istradefylline 20 mg/day (-0.99 hours, P=.003) and istradefylline 40 mg/day (-0.96 hours, P=.003) groups compared with the placebo group (-0.23 hours). The most common adverse event was dyskinesia (placebo, 4.0%; istradefylline 20 mg/day, 13.0%; istradefylline 40 mg/day, 12.1%).

Conclusions: Istradefylline reduced daily OFF time and was well tolerated in Japanese PD patients with motor complications on levodopa treatment.

Keywords: Parkinson's disease; istradefylline; levodopa; motor complications; wearing-off.

Publication types

  • Multicenter Study
  • Randomized Controlled Trial
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adenosine A2 Receptor Antagonists / therapeutic use*
  • Aged
  • Dose-Response Relationship, Drug
  • Double-Blind Method
  • Female
  • Humans
  • Japan
  • Male
  • Middle Aged
  • Parkinson Disease / drug therapy*
  • Purines / therapeutic use*
  • Retrospective Studies
  • Treatment Outcome

Substances

  • Adenosine A2 Receptor Antagonists
  • Purines
  • istradefylline