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Trial details imported from ClinicalTrials.gov
For full trial details, please see the original record at
https://clinicaltrials.gov/study/NCT00335166
Registration number
NCT00335166
Ethics application status
Date submitted
8/06/2006
Date registered
9/06/2006
Date last updated
3/04/2008
Titles & IDs
Public title
SLV 308 and Pramipexole for Treatment of Patients With Early Parkinson Disease
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Scientific title
A Multicenter, Randomized, Double Blind, Parallel-Group Placebo and Pramipexole Controlled Study to Assess Efficacy and Safety of SLV308 Monotherapy in the Treatment of Patients With Early Stage Parkinson's Disease.
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Secondary ID [1]
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Not requested yet
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Secondary ID [2]
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S308.3.003
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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 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 - Pardaprunox
Treatment: Drugs - pramipexole
Treatment: Drugs - Placebo Comparator
Experimental: 1 -
Active comparator: 2 -
Placebo comparator: 3 -
Treatment: Drugs: Pardaprunox
12-42 mg
Treatment: Drugs: pramipexole
1.5-4.5 mg
Treatment: Drugs: Placebo Comparator
Placebo
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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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UPDRS part 3 (motor score)and change from baseline to 24 weeks maintenance treatment
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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 part 2 (ADL score); CGI-Improvement; PDQ-39 total score: all change from baseline to 24 weeks maintenance treatment.
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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
* Diagnosis of idiopathic Parkinson's Disease, Modified Hoehn & Yahr up to stage III, UPDRS motor score (part III) must have a total of at least 10 at baseline.
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Minimum age
30
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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
* Diagnosis is unclear or a suspicion of other parkinsonian syndromes,
* Patients who have undergone surgery for the treatment of PD,
* Current presence of dyskinesias,
* Motor fluctuations or loss of postural reflexes,
* A history of non-response to an adequate course of l-dopa or a dopamine agonist,
* Patients for whom previously treatment with dopamine agonists needed to terminate because of induction of psychosis (i.e. hallucinations) and /or sleep attacks.
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Study design
Purpose of the study
Treatment
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Allocation to intervention
Randomised controlled 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
Blinded (masking used)
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Who is / are masked / blinded?
The people receiving the treatment/s
The people administering the treatment/s
The people assessing the outcomes
The people analysing the results/data
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Intervention assignment
Parallel
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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
1/11/2006
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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
1/02/2008
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Sample size
Target
330
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Accrual to date
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Final
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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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301 - Concord
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302 - Westmead
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- Bedford Park
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- Cheltenham
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Recruitment postcode(s) [3]
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- Concord
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Recruitment postcode(s) [4]
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- Westmead
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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, randomized, double blind, parallel group study of 6 months' treatment with SLV308 as monotherapy in patients with early stage PD. An open label safety extension to this study is planned as a separate protocol for patients who are willing and eligible to participate.
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Trial website
https://clinicaltrials.gov/study/NCT00335166
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Trial related presentations / publications
Sampaio C, Bronzova J, Hauser RA, Lang AE, Rascol O, van de Witte SV, Theeuwes AA; Rembrandt/Vermeer Study Groups. Pardoprunox in early Parkinson's disease: results from 2 large, randomized double-blind trials. Mov Disord. 2011 Jul;26(8):1464-76. doi: 10.1002/mds.23590. Epub 2011 May 3.
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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/NCT00335166
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