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Completed Phase 3 Interventional

An Open Label SLV308 Safety Extension to Study S308.3.001 in Early PD Patients

ClinicalTrials.gov ID: NCT00332917

Public ClinicalTrials.gov record NCT00332917. 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, 1:36 PM EDT

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

Brief summary

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

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 S308.3.001 trial

Study identification

NCT ID
NCT00332917
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
Solvay Pharmaceuticals
Industry
Enrollment
224 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
Jan 31, 2007
Primary completion
Jun 30, 2008
Completion
Jun 30, 2008
Last update posted
Jan 25, 2009

2007 – 2008

United States locations

U.S. sites
25
U.S. states
16
U.S. cities
24
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 270 Bennington Vermont — —

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 105 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00332917, 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 Jan 25, 2009 · Synced Sep 26, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT00332917 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →