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A Double-Blind, Placebo-Controlled, Multicenter, Multinational Phase III Study to Evaluate the Safety and Efficacy of Sarizotan in Patients With Parkinson's Disease Suffering From Treatment-Associated Dyskinesia
The purpose of this study is to test multiple doses of sarizotan to establish a dose with maximal safety and efficacy for treating treatment associated dyskinesia in Parkinson's disease participants.
Age
30 - No limit years
Sex
ALL
Healthy Volunteers
No
Phoenix, Arizona, United States
Phoenix, Arizona, United States
Phoenix, Arizona, United States
Scottsdale, Arizona, United States
Fayetteville, Arkansas, United States
Fountain Valley, California, United States
Los Angeles, California, United States
Fort Lauderdale, Florida, United States
Hollywood, Florida, United States
Ocala, Florida, United States
Start Date
September 30, 2004
Primary Completion Date
March 31, 2006
Completion Date
March 31, 2006
Last Updated
April 2, 2018
398
ACTUAL participants
Sarizotan
DRUG
Placebo
DRUG
Lead Sponsor
EMD Serono
NCT02119611
NCT07310264
Data Source & Attribution
This clinical trial information is sourced from ClinicalTrials.gov, a service of the U.S. National Institutes of Health.
Modifications: This data has been reformatted for display purposes. Eligibility criteria have been parsed into inclusion/exclusion sections. Location data has been geocoded to enable distance-based search. For the authoritative and most current information, please visit ClinicalTrials.gov.
Neither the United States Government nor Clareo Health make any warranties regarding the data. Check ClinicalTrials.gov frequently for updates.
View ClinicalTrials.gov Terms and ConditionsNCT07216976