ClinicalTrials.gov record
Completed Phase 3 Interventional

SLV 308 and Pramipexole for Treatment of Patients With Early Parkinson Disease

ClinicalTrials.gov ID: NCT00335166

Public ClinicalTrials.gov record NCT00335166. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced May 6, 2026, 2:05 AM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official 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.

Study identification

NCT ID
NCT00335166
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
Solvay Pharmaceuticals
Industry
Enrollment
330 participants

Conditions and interventions

Interventions

  • Pardaprunox Drug
  • Placebo Comparator Drug
  • pramipexole Drug

Drug

Eligibility (public fields only)

Age range
30 Years and older
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Oct 31, 2006
Primary completion
Jan 31, 2008
Completion
Jan 31, 2008
Last update posted
Apr 2, 2008

2006 – 2008

United States locations

U.S. sites
17
U.S. states
12
U.S. cities
16
Facility City State ZIP Site status
419 Birmingham Alabama
413 Oceanside California
408 Oxnard California
422 New Haven Connecticut
403 Boca Raton Florida
411 Sarasota Florida
421 Augusta Georgia
410 Fort Wayne Indiana
417 Lexington Kentucky
405 Boston Massachusetts
420 Boston Massachusetts
415 Grand Rapids Michigan
416 Golden Valley Minnesota
406 Minneapolis Minnesota
418 Albany New York
424 Charlotte North Carolina
412 Raleigh North Carolina

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 72 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00335166, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Apr 2, 2008 · Synced May 6, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT00335166 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →