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Trial details imported from ClinicalTrials.gov
For full trial details, please see the original record at
https://clinicaltrials.gov/study/NCT00335374
Registration number
NCT00335374
Ethics application status
Date submitted
8/06/2006
Date registered
9/06/2006
Date last updated
6/02/2009
Titles & IDs
Public title
An Open Label SLV308 Safety Extension to Study S308.3.003 in Early PD Patients
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Scientific title
An Open Label SLV308 Safety Extension to Study S308.3.003 in Early PD Patients
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Secondary ID [1]
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2006-000859-18
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Secondary ID [2]
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S308.3.008
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Universal Trial Number (UTN)
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Trial acronym
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Linked study record
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Health condition
Health condition(s) or problem(s) studied:
Early Stage Parkinson's Disease
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Condition category
Condition code
Neurological
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Parkinson's disease
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Intervention/exposure
Study type
Interventional
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Description of intervention(s) / exposure
Treatment: Drugs - Pardoprunox
Experimental: 1 -
Treatment: Drugs: Pardoprunox
12 -42 mg
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Intervention code [1]
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Treatment: Drugs
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Comparator / control treatment
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Control group
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Outcomes
Primary outcome [1]
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Safety: laboratory data, adverse events, vital signs, ECG
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Assessment method [1]
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Timepoint [1]
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24 weeks
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Secondary outcome [1]
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UPDRS parts 1, 2 and 3, CGI-severity, CGI-Improvement, PDQ-39 total score: all change from baseline
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Assessment method [1]
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Timepoint [1]
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24 weeks
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Eligibility
Key inclusion criteria
* Patients who have completed S308.3.003 trial
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Minimum age
30
Years
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Maximum age
No limit
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Sex
Both males and females
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Can healthy volunteers participate?
No
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Key exclusion criteria
* Patients with medically relevant abnormal findings (ECG, physical examination, AEs) at end of the maintenance phase (visit M6, week 24) of study S308.3.003
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Study design
Purpose of the study
Treatment
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Allocation to intervention
Non-randomised trial
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Procedure for enrolling a subject and allocating the treatment (allocation concealment procedures)
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Methods used to generate the sequence in which subjects will be randomised (sequence generation)
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Masking / blinding
Open (masking not used)
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Who is / are masked / blinded?
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Intervention assignment
Single group
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Other design features
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Phase
Phase 3
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Type of endpoint/s
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Statistical methods / analysis
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Recruitment
Recruitment status
Completed
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Data analysis
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Reason for early stopping/withdrawal
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Other reasons
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Date of first participant enrolment
Anticipated
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Actual
1/08/2007
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Date of last participant enrolment
Anticipated
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Actual
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Date of last data collection
Anticipated
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Actual
1/11/2008
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Sample size
Target
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Accrual to date
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Final
202
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Recruitment in Australia
Recruitment state(s)
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Recruitment hospital [1]
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303 - Bedford Park
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Recruitment hospital [2]
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304 - Cheltenham
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Recruitment hospital [3]
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301 - Concord
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Recruitment hospital [4]
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Site 300 - East Gosford
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Recruitment hospital [5]
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302 - Westmead
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Recruitment postcode(s) [1]
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- Bedford Park
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- Cheltenham
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- Concord
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Recruitment postcode(s) [4]
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- East Gosford
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Recruitment postcode(s) [5]
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- Westmead
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United States of America
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Alabama
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Funding & Sponsors
Primary sponsor type
Commercial sector/industry
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Name
Solvay Pharmaceuticals
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Address
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Ethics approval
Ethics application status
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Summary
Brief 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
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Trial website
https://clinicaltrials.gov/study/NCT00335374
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Trial related presentations / publications
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Public notes
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Contacts
Principal investigator
Name
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Global Clinical Director Solvay
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Address
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Solvay Pharmaceuticals
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Contact person for scientific queries
No information has been provided regarding IPD availability
What supporting documents are/will be available?
No Supporting Document Provided
Results publications and other study-related documents
No documents have been uploaded by study researchers.
Results not provided in
https://clinicaltrials.gov/study/NCT00335374
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