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An Open Label SLV308 Safety Extension to Study S308.3.003 in Early PD Patients

NCT00335374 · Status: COMPLETED · Phase: PHASE3 · Type: INTERVENTIONAL · Enrollment: 202

Last updated 2009-02-06

No results posted yet for this study

Summary

This is a multicenter, 6 months open label safety extension study for all patients who are willing and eligible to continue from the pivotal, double-blind S308.3.003 trial

Conditions

  • Early Stage Parkinson's Disease

Interventions

DRUG

Pardoprunox

12 -42 mg

Sponsors & Collaborators

  • Solvay Pharmaceuticals

    lead INDUSTRY

Principal Investigators

  • Global Clinical Director Solvay · Solvay Pharmaceuticals

Study Design

Allocation
NON_RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
30 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2007-08-31
Primary Completion
2008-09-30
Completion
2008-11-30

Countries

  • United States
  • Australia
  • Czechia
  • Estonia
  • Germany
  • India
  • Italy
  • Lithuania
  • Malaysia
  • Netherlands
  • Poland
  • Portugal
  • South Africa
  • Taiwan
  • Thailand

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT00335374 on ClinicalTrials.gov