Clinical Trial Comparing Single-administration of DA-5222 and Co-administration of DA-5222-R1, DA-5222-R2 and DA-5222-R3 in Healthy Adult Subjects in Fed State
NCT ID: NCT07046715
Last Updated: 2025-11-17
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
40 participants
INTERVENTIONAL
2025-07-07
2025-08-19
Brief Summary
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Detailed Description
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Conditions
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Study Design
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RANDOMIZED
CROSSOVER
TREATMENT
NONE
Study Groups
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Sequence A
DA-5222
single dose administration (DA-5222 one tablet once a day)
DA-5222-R1
single dose administration (DA-5222-R1 one tablet once a day)
DA-5222-R2
single dose administration (DA-5222-R2 one tablet once a day)
DA-5222-R3
single dose administration (DA-5222-R3 one tablet once a day)
Sequence B
DA-5222
single dose administration (DA-5222 one tablet once a day)
DA-5222-R1
single dose administration (DA-5222-R1 one tablet once a day)
DA-5222-R2
single dose administration (DA-5222-R2 one tablet once a day)
DA-5222-R3
single dose administration (DA-5222-R3 one tablet once a day)
Interventions
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DA-5222
single dose administration (DA-5222 one tablet once a day)
DA-5222-R1
single dose administration (DA-5222-R1 one tablet once a day)
DA-5222-R2
single dose administration (DA-5222-R2 one tablet once a day)
DA-5222-R3
single dose administration (DA-5222-R3 one tablet once a day)
Eligibility Criteria
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Inclusion Criteria
* BMI between 18 and 30 kg/m2
* Body weight: Male≥50kg, Female≥45kg
* Subjects who have signed an informed consent themselves after receiving detailed explanation about clinical study
Exclusion Criteria
* Subjects with history of drug abuse or addicted
* Subjects with allergy or drug hypersensitivity
19 Years
ALL
Yes
Sponsors
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Dong-A ST Co., Ltd.
INDUSTRY
Responsible Party
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Locations
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Bumin Hospital
Seoul, Gangseo-gu, South Korea
Countries
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Other Identifiers
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DA5222_BEF_I
Identifier Type: -
Identifier Source: org_study_id
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