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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
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.
Secondary ID [1] 0 0
Not requested yet
Secondary ID [2] 0 0
S308.3.003
Universal Trial Number (UTN)
Trial acronym
Linked study record

Health condition
Health condition(s) or problem(s) studied:
Early Stage Parkinson Disease 0 0
Condition category
Condition code
Neurological 0 0 0 0
Parkinson's disease

Intervention/exposure
Study type
Interventional
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

Intervention code [1] 0 0
Treatment: Drugs
Comparator / control treatment
Control group

Outcomes
Primary outcome [1] 0 0
UPDRS part 3 (motor score)and change from baseline to 24 weeks maintenance treatment
Timepoint [1] 0 0
24 weeks
Secondary outcome [1] 0 0
UPDRS part 2 (ADL score); CGI-Improvement; PDQ-39 total score: all change from baseline to 24 weeks maintenance treatment.
Timepoint [1] 0 0
24 weeks

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.
Minimum age
30 Years
Maximum age
No limit
Sex
Both males and females
Can healthy volunteers participate?
No
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.

Study design
Purpose of the study
Treatment
Allocation to intervention
Randomised controlled trial
Procedure for enrolling a subject and allocating the treatment (allocation concealment procedures)
Methods used to generate the sequence in which subjects will be randomised (sequence generation)
Masking / blinding
Blinded (masking used)
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
Intervention assignment
Parallel
Other design features
Phase
Phase 3
Type of endpoint/s
Statistical methods / analysis

Recruitment
Recruitment status
Completed
Data analysis
Reason for early stopping/withdrawal
Other reasons
Date of first participant enrolment
Anticipated
Actual
Date of last participant enrolment
Anticipated
Actual
Date of last data collection
Anticipated
Actual
Sample size
Target
Accrual to date
Final
Recruitment in Australia
Recruitment state(s)
Recruitment hospital [1] 0 0
303 - Bedford Park
Recruitment hospital [2] 0 0
304 - Cheltenham
Recruitment hospital [3] 0 0
301 - Concord
Recruitment hospital [4] 0 0
302 - Westmead
Recruitment postcode(s) [1] 0 0
- Bedford Park
Recruitment postcode(s) [2] 0 0
- Cheltenham
Recruitment postcode(s) [3] 0 0
- Concord
Recruitment postcode(s) [4] 0 0
- Westmead
Recruitment outside Australia
Country [1] 0 0
United States of America
State/province [1] 0 0
Alabama
Country [2] 0 0
United States of America
State/province [2] 0 0
California
Country [3] 0 0
United States of America
State/province [3] 0 0
Connecticut
Country [4] 0 0
United States of America
State/province [4] 0 0
Florida
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United States of America
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Georgia
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United States of America
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Indiana
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United States of America
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Kentucky
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United States of America
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Massachusetts
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United States of America
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Michigan
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United States of America
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Minnesota
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New York
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North Carolina
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Czech Republic
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Kralove
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Czech Republic
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Olomouc
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Czech Republic
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Ostrava
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Czech Republic
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Pardubice
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Czech Republic
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Plzen
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Estonia
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Tallinn
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Estonia
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Tartu
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France
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Aix en Provence
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France
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Toulon
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France
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Toulouse
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Germany
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Bochum
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Germany
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Gottingen
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Germany
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Heidelberg
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Germany
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Homburg
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Germany
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Leipzig
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Germany
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Lubeck
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Germany
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Wiesbaden
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India
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Bangalore
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India
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Hyderabad
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India
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Kerala
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India
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Mumbai
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Italy
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Arcugnano (VI)
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Italy
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Grosseto GR
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Italy
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Lido di Camaiore (LU)
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Italy
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Pescara
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Italy
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Roma
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Lithuania
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Kaunas
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Lithuania
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Vilnius
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Malaysia
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Kelantan
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Malaysia
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Kuala Lumpur
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Eindhoven
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Emmen
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Groningen
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Hertogenbosch
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RM Groningen
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Gdansk
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Kalisz
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Katowice
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Krakow
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Leszno
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Lublin
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Mosina
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Torun
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Portugal
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Coimbra
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Portugal
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Lisboa
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South Africa
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Cape Town
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South Africa
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Gauteng
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South Africa
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Pretoria
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South Africa
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Sandton
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Spain
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Barcelona
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Spain
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Colmenar Viejo
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Spain
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San Sebastian
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Taiwan
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Hualien
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Kaohsiung Hsien
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Kaohsiung
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Kweishan
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Taipei
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Thailand
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Bangkok
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Thailand
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Ubonratchathani Province
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United Kingdom
State/province [73] 0 0
Blackpool

Funding & Sponsors
Primary sponsor type
Commercial sector/industry
Name
Solvay Pharmaceuticals
Address
Country

Ethics approval
Ethics application status

Summary
Brief summary
Trial website
Trial related presentations / publications
Public notes

Contacts
Principal investigator
Name 0 0
Global Clinical Director Solvay
Address 0 0
Solvay Pharmaceuticals
Country 0 0
Phone 0 0
Fax 0 0
Email 0 0
Contact person for public queries
Name 0 0
Address 0 0
Country 0 0
Phone 0 0
Fax 0 0
Email 0 0
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.