Clinical Trial of Comparing DA-2902 and DA-2902-R in Healthy Adult Subjects
NCT ID: NCT07239453
Last Updated: 2025-11-20
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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ENROLLING_BY_INVITATION
PHASE1
40 participants
INTERVENTIONAL
2025-10-20
2025-12-31
Brief Summary
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Detailed Description
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Conditions
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Study Design
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RANDOMIZED
CROSSOVER
TREATMENT
NONE
Study Groups
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Sequence A
DA-2902
single dose administration (DA-2902 one tablet once a day)
DA-2902-R
single dose administration (DA-2902-R one tablet once a day)
Sequence B
DA-2902
single dose administration (DA-2902 one tablet once a day)
DA-2902-R
single dose administration (DA-2902-R one tablet once a day)
Interventions
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DA-2902
single dose administration (DA-2902 one tablet once a day)
DA-2902-R
single dose administration (DA-2902-R 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
44 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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CHA University Bundang Medical Center
Seongnam-si, Gyeonggi-do, South Korea
Countries
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Other Identifiers
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DA2902_BE_I
Identifier Type: -
Identifier Source: org_study_id
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