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Completed Phase 3 Interventional Results available

Sarizotan HC1 in Patients With Parkinson's Disease Suffering From Treatment-associated Dyskinesia

ClinicalTrials.gov ID: NCT00105508

Public ClinicalTrials.gov record NCT00105508. 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 Apr 22, 2026, 11:19 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 Double-blind, Placebo-controlled, Multicenter, Multinational Phase III Study to Evaluate the Safety and Efficacy of Sarizotan HCl 1 mg b.i.d. in Patients With Parkinson's Disease Suffering From Treatment-associated Dyskinesia

Study identification

NCT ID
NCT00105508
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
EMD Serono
Industry
Enrollment
506 participants

Conditions and interventions

Interventions

  • Placebo Drug
  • Sarizotan Drug

Drug

Eligibility (public fields only)

Age range
30 Years and older
Sex
All
Healthy volunteers
Not listed

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

Study timeline

Start date
Sep 29, 2004
Primary completion
Feb 27, 2006
Completion
Feb 27, 2006
Last update posted
Jul 25, 2018

2004 – 2006

United States locations

U.S. sites
31
U.S. states
21
U.S. cities
29
Facility City State ZIP Site status
Not listed Birmingham Alabama 35233
Not listed Huntsville Alabama 35801
Not listed La Jolla California 92037
Not listed Oxnard California 93030
Not listed Sacramento California 95817
Not listed Englewood Colorado 80113
Not listed Danbury Connecticut 06810
Not listed Farmington Connecticut 06030-1840
Not listed Jacksonville Florida 32209
Not listed Jacksonville Florida 32216
Not listed Maitland Florida 32751
Not listed St. Petersburg Florida 33703
Not listed Decatur Georgia 30033
Not listed Chicago Illinois 60611-3078
Not listed Springfield Illinois 62702
Not listed Des Moines Iowa 50309
Not listed New Orleans Louisiana 70112
Not listed Scarborough Maine 04074
Not listed Boston Massachusetts 02215
Not listed Southfield Michigan 48034
Not listed Edison New Jersey 08818
Not listed New Hyde Park New York 11040
Not listed New Hyde Park New York 12401
Not listed New York New York 10016
Not listed Durham North Carolina 27705
Not listed Oklahoma City Oklahoma 73104
Not listed Pittsburgh Pennsylvania 15213
Not listed Brentwood Tennessee 37027
Not listed South Ogden Utah 84403
Not listed Spokane Washington 99204
Not listed Milwaukee Wisconsin 53233

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

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00105508, 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 Jul 25, 2018 · Synced Apr 22, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT00105508 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →