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This study is a multicenter, 9 months, open label extension study for all patients who are willing and eligible to continue from the pivotal, double-blind S308.3.002 study.
Age
30 - No limit years
Sex
ALL
Healthy Volunteers
No
S308.3.007 Site # 220
La Jolla, California, United States
S308.3.007 Site # 211
San Francisco, California, United States
S308.3.007 Site # 214
Fort Lauderdale, Florida, United States
S308.3.007 Site # 218
Gainsville, Florida, United States
S308.3.007 Site # 213
Tampa, Florida, United States
S308.3.007 Site # 219
Augusta, Georgia, United States
S308.3.007 Site # 221
Chicago, Illinois, United States
S308.3.007 Site # 216
Kansas City, Kansas, United States
S308.3.007 Site # 224
Lexington, Kentucky, United States
S308.3.007 Site # 212
East Lansing, Michigan, United States
Start Date
August 1, 2007
Primary Completion Date
May 1, 2009
Completion Date
May 1, 2009
Last Updated
September 13, 2010
140
ESTIMATED participants
Pardoprunox
DRUG
Lead Sponsor
Solvay Pharmaceuticals
NCT00501969
NCT00903838
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.
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