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Clinical Trial Summary

To investigate superiority of SPM 962 over placebo in early Parkinson's disease patients in a multi-center, placebo-controlled, double-blind study following once-daily multiple transdermal doses of SPM 962 within a range of 4.5 to 36.0 mg (12-week dose titration/maintenance period)


Clinical Trial Description

n/a


Study Design

Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Caregiver, Investigator, Outcomes Assessor), Primary Purpose: Treatment


Related Conditions & MeSH terms


NCT number NCT00537485
Study type Interventional
Source Otsuka Pharmaceutical Co., Ltd.
Contact
Status Completed
Phase Phase 2/Phase 3
Start date September 2007
Completion date December 2009

See also
  Status Clinical Trial Phase
Active, not recruiting NCT04269642 - SR-Exenatide (PT320) to Eveluate Efficacy and Safety in Patients With Early Parkinson's Disease Phase 2
Completed NCT03329508 - A Phase 3 Study With P2B001 in Subjects With Early Parkinson's Phase 3