Literature DB >> 23589371

Long-term safety and efficacy of preladenant in subjects with fluctuating Parkinson's disease.

Stewart A Factor1, Kenneth Wolski, Daniel M Togasaki, Susan Huyck, Marc Cantillon, T W Ho, Robert A Hauser, Emmanuelle Pourcher.   

Abstract

BACKGROUND: Preladenant is a selective adenosine A₂A receptor antagonist under investigation for Parkinson's disease treatment.
METHODS: A phase 2 36-week open-label follow-up of a double-blind study using preladenant 5 mg twice a day as a levodopa adjunct in 140 subjects with fluctuating Parkinson's disease was conducted. The primary end point was adverse event (AE) assessment. Secondary (efficacy) analyses included hours/day spent in OFF and ON states and dyskinesia prevalence/severity.
RESULTS: The 36-week open-label phase was completed by 106 of 140 subjects (76%). AE-related treatment discontinuations occurred in 19 subjects (14%). Treatment-emergent AEs, reported by ≥15% of subjects, were dyskinesia (33%) and constipation (19%). Preladenant 5 mg twice a day provided OFF time reductions (1.4-1.9 hours/day) and ON time increases (1.2-1.5 hours/day) throughout the 36-week treatment relative to the baseline of the double-blind study.
CONCLUSIONS: Long-term preladenant treatment (5 mg twice a day) was generally well tolerated and provided sustained OFF time reductions and ON time increases.
Copyright © 2013 Movement Disorder Society.

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Year:  2013        PMID: 23589371     DOI: 10.1002/mds.25395

Source DB:  PubMed          Journal:  Mov Disord        ISSN: 0885-3185            Impact factor:   10.338


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