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
PHASE1
18 participants
INTERVENTIONAL
2013-09-30
2013-12-31
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
BASIC_SCIENCE
QUADRUPLE
Study Groups
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FYU-981
FYU-981, (Oral daily dosing for 7 days)
Subjects randomized to the FYU-981 arm receive active drug, FYU-981.
Placebo
Placebo, (Oral daily dosing for 7 days)
Subjects randomized to the placebo arm receive placebo.
Interventions
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FYU-981, (Oral daily dosing for 7 days)
Subjects randomized to the FYU-981 arm receive active drug, FYU-981.
Placebo, (Oral daily dosing for 7 days)
Subjects randomized to the placebo arm receive placebo.
Eligibility Criteria
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Inclusion Criteria
* Body mass index: \>=18.5 and \<25.0
Exclusion Criteria
20 Years
35 Years
MALE
Yes
Sponsors
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Fuji Yakuhin Co., Ltd.
INDUSTRY
Responsible Party
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Locations
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Japan
Tokyo, , Japan
Countries
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Other Identifiers
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FYU-981-002
Identifier Type: -
Identifier Source: org_study_id
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