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Safety and efficacy of newly formulated selegiline orally disintegrating tablets as an adjunct to levodopa in the management of 'off' episodes in patients with Parkinson's disease

  • Mark F. Lew(corresponding author)
    ,
  • Rajesh Pahwa
    ,
  • Maureen Leehey
    ,
  • John Bertoni
    ,
  • Greg Kricorian
    ,
  • Brian H. Avin
*Corresponding author for this work
  • University of Southern California
    ,
  • University of Kansas
    ,
  • University of Colorado Denver
    ,
  • Creighton University
    ,
  • Valeant Pharmaceuticals International
    ,
Scholary Output:
Contribution to journal
Article
Peer-review

Abstract

Objective: Patients receiving levodopa for Parkinson's disease experience motor fluctuations and immobility ('off' episodes) between doses. This study assessed adjunctive Zelaparf (selegiline orally disintegrating tablet (ODT)) for managing off episodes and for long-term safety. Methods: This open-label extension evaluated long-term safety, efficacy, and tolerability of adjunctive selegiline ODT 2.5 mg in patients who completed either of two large phase 3 double-blind studies. The study was to end after 12 months but was amended to be open-ended. Investigators could increase levodopa doses and introduce controlled-release formulations of levodopa or dopamine agonists if warranted. Additionally, results of a small randomized trial of open-label selegiline ODT 1.25 mg in comparison to conventional selegiline was added only to the safety analysis. Efficacy variables included changes in daily off time and Patient's Global Impression of Improvement (PGM) and Clinical Global Impressions Severity of Disease (CGI-S) ratings. Safety assessments included adverse events and oropharyngeal findings. Results: This study enrolled 254 patients: 248 from the large phase 3 studies (efficacy analysis) and an additional six from the prior open-label comparison (safety analysis) in order to evaluate a larger population for safety purposes. Mean reduction from baseline in daily off time was 9.4% (1.6h) for patients previously given selegiline ODT, 6.0% (1.2h) for those switched from placebo, and 8.1% (1.4h) overall. PGI-I and CGI-S ratings indicated little or no change from baseline. Treatment-related adverse events occurred in 132 (52%) patients. No severe oral irritations were attributed to selegiline ODT or prompted discontinuation. Conclusions: Long-term selegiline ODT 2.5 mg/day was effective, safe, and well tolerated in patients with Parkinson's disease experiencing off episodes during levodopa therapy.

Publication Information

Output type

Scholary Output:
Contribution to journal
Article
Peer-review

Original language

English (US)

Pages from-to (Number of pages)

Pages 741-750 (10 pages)

Journal (Volume, Issue Number)

Current Medical Research and Opinion (Volume 23, Issue 4)

Publication milestones

  • Published - 04/2007

Publication status

Published - 04/2007

ISSN

0300-7995

Publication IDs

  • Scopus: 34247324279
  • PubMed: 17407630

Publication metrics

Metrics

Scopus
citations
SciVal
FWCI
3.34
SciVal
Author count
30
SciVal
citations
25
SciVal
Paper percentile
77
Fractional count
1
Fractional count
0.03
Fractional count
29
Fractional count
0.97
Fractional count
1
Fractional count
1

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Citation count
27
Captures
46

Funding Details

The extension study reported in this manuscript was funded by Valeant Pharmaceuticals International, Aliso Viejo, CA, USA. The authors wish to acknowledge Michael McLaughlin, MD, for his editorial assistance during the preparation of this manuscript.
FunderFunding numbers
Valeant Pharmaceuticals International
-