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Completed Phase 3 Interventional

SLV308 for Treatment of Patients With Early Parkinson's Disease

ClinicalTrials.gov ID: NCT00269516

Public ClinicalTrials.gov record NCT00269516. 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 Sep 26, 2026, 1:34 PM 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 Randomized, Double Blind, Placebo Controlled Parallel-Group Fixed and Flexible SLV308 Dose Arm Study to Assess Efficacy and Safety of SLV308 Monotherapy in the Treatment of Patients With Early Stage Parkinson's Disease

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

This study is a multicenter, randomized, double blind, parallel group study of 6 months' treatment with SLV308 administered as a 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.

Study identification

NCT ID
NCT00269516
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
Solvay Pharmaceuticals
Industry
Enrollment
468 participants

Conditions and interventions

Interventions

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
May 31, 2006
Primary completion
Nov 30, 2007
Completion
Nov 30, 2007
Last update posted
Aug 28, 2008

2006 – 2007

United States locations

U.S. sites
24
U.S. states
15
U.S. cities
23
Facility City State ZIP Site status
Site 284 Huntsville Alabama — —
Site 274 Little Rock Arkansas — —
Site 283 Fountain Valley California — —
Site 277 La Jolla California — —
Site 271 San Francisco California — —
Site 279 Fort Lauderdale Florida — —
Site 293 Gainsville Florida — —
Site 282 Port Charlotte Florida — —
Site 285 Sunrise Florida — —
Site 273 Tampa Florida — —
Site 290 Chicago Illinois — —
Site 280 Kansas City Kansas — —
Site 292 Bingham Farms Michigan — —
Site 275 Traverse City Michigan — —
Site 276 St Louis Missouri — —
Site 287 St Louis Missouri — —
Site 278 Las Vegas Nevada — —
Site 286 Rochester New York — —
Site 288 Ashville North Carolina — —
Site 289 Charlotte North Carolina — —
Site 294 Toledo Ohio — —
Site 281 Pittsburgh Pennsylvania — —
Site 291 Warwick Rhode Island — —
Site 272 Houston Texas — —

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 104 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00269516, 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 Aug 28, 2008 · Synced Sep 26, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT00269516 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →