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CompletedNCT00537485

A Placebo-controlled Study for SPM 962 in Early Parkinson's Disease Patients

A Placebo-controlled Study for SPM 962 in Early Parkinson's Disease Patients With Non-concomitant Treatment of L-dopa

Status
Completed
Phase
Phase 2 / Phase 3
Study type
Interventional
Enrollment
180 (actual)
Sponsor
Otsuka Pharmaceutical Co., Ltd. · Industry
Sex
All
Age
30 Years – 79 Years
Healthy volunteers
Not accepted

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)

Conditions

Interventions

TypeNameDescription
DRUGSPM 962transdermal application, 1 time per day
DRUGplacebotransdermal application, 1 time per day

Timeline

Start date
2007-09-01
Primary completion
2009-12-01
Completion
2009-12-01
First posted
2007-10-01
Last updated
2014-03-19
Results posted
2014-03-19

Locations

6 sites across 1 country: Japan

Source: ClinicalTrials.gov record NCT00537485. Inclusion in this directory is not an endorsement.

A Placebo-controlled Study for SPM 962 in Early Parkinson's Disease Patients (NCT00537485) · Clinical Trials Directory