Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
PHASE3
322 participants
INTERVENTIONAL
2011-07-31
2012-03-31
Brief Summary
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Detailed Description
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Conditions
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Keywords
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Study Design
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RANDOMIZED
PARALLEL
TREATMENT
QUADRUPLE
Study Groups
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Active
Product 33525
33525
Daily for 14 days
Placebo
Product 33525 Placebo
Placebo
Daily for 14 days
Interventions
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33525
Daily for 14 days
Placebo
Daily for 14 days
Eligibility Criteria
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Inclusion Criteria
Exclusion Criteria
12 Years
ALL
No
Sponsors
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Medicis Global Service Corporation
INDUSTRY
Responsible Party
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Principal Investigators
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Ron Staugaard
Role: STUDY_DIRECTOR
Medicis Pharmaceutical
Locations
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Miami, Florida, United States
Miramar, Florida, United States
Augusta, Georgia, United States
Evansville, Indiana, United States
Warren, Michigan, United States
Hackensack, New Jersey, United States
High Point, North Carolina, United States
Cinncinnati, Ohio, United States
Philadelphia, Pennsylvania, United States
Nashville, Tennessee, United States
Belize City, , Belize
Countries
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Other Identifiers
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MP-1000-03
Identifier Type: -
Identifier Source: org_study_id