Phase 2 Study of OPA-15406 Ointment in Pediatric Patients With Atopic Dermatitis
NCT ID: NCT03018691
Last Updated: 2020-07-23
Study Results
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View full resultsBasic Information
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COMPLETED
PHASE2
73 participants
INTERVENTIONAL
2017-01-31
2017-06-30
Brief Summary
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Detailed Description
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Conditions
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Study Design
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RANDOMIZED
PARALLEL
TREATMENT
QUADRUPLE
Study Groups
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0.3% OPA-15406 Ointments
Subjects were treated with assigned 0.3% OPA-15406 ointment twice daily.
OPA-15406
1% OPA-15406 Ointments
Subjects were treated with assigned 1% OPA-15406 ointment twice daily.
OPA-15406
Placebo Ointments
Subjects were treated with assigned 0% OPA-15406 ointment twice daily.
Placebos
Interventions
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OPA-15406
Placebos
Eligibility Criteria
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Inclusion Criteria
Exclusion Criteria
* Subjects who have an active viral skin infection.
* Subjects with a current or history of malignancy.
2 Years
14 Years
ALL
No
Sponsors
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Otsuka Pharmaceutical Co., Ltd.
INDUSTRY
Responsible Party
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Principal Investigators
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Hiroaki Ono, Mr
Role: STUDY_DIRECTOR
Otsuka Pharmaceutical Co., Ltd.
Locations
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Hokkaido Region, , Japan
Kanto Region, , Japan
Kinki Region, , Japan
Kyushu Region, , Japan
Countries
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Provided Documents
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Document Type: Study Protocol
Document Type: Statistical Analysis Plan
Other Identifiers
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JapicCTI-173484
Identifier Type: OTHER
Identifier Source: secondary_id
271-102-00002
Identifier Type: -
Identifier Source: org_study_id
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