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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RECRUITING
PHASE3
252 participants
INTERVENTIONAL
2024-04-15
2025-07-31
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
TREATMENT
DOUBLE
Study Groups
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AD-224A
AD-224A+Placebo of AD-224B+Placebo of AD-224C
AD-224A
PO, Once daily, 8weeks
Placebo of AD-224B
PO, Once daily, 8weeks
Placebo of AD-224C
PO, Once daily, 8weeks
AD-224B
Placebo of AD-224A+AD-224B+Placebo of AD-224C
AD-224B
PO, Once daily, 8weeks
Placebo of AD-224A
PO, Once daily, 8weeks
Placebo of AD-224C
PO, Once daily, 8weeks
AD-224C
Placebo of AD-224A+Placebo of AD-224B+AD-224C
AD-224C
PO, Once daily, 8weeks
Placebo of AD-224A
PO, Once daily, 8weeks
Placebo of AD-224B
PO, Once daily, 8weeks
Interventions
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AD-224A
PO, Once daily, 8weeks
AD-224B
PO, Once daily, 8weeks
AD-224C
PO, Once daily, 8weeks
Placebo of AD-224A
PO, Once daily, 8weeks
Placebo of AD-224B
PO, Once daily, 8weeks
Placebo of AD-224C
PO, Once daily, 8weeks
Eligibility Criteria
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Inclusion Criteria
* Patients with Essential Hypertension
* Other inclusions applied
Exclusion Criteria
* Other exclusions applied
19 Years
ALL
No
Sponsors
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Addpharma Inc.
INDUSTRY
Responsible Party
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Principal Investigators
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InHo Chae, M.D., Ph.D
Role: PRINCIPAL_INVESTIGATOR
Seoul National University Bundang Hospital
Locations
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Seoul National University Bundang Hospital
Seongnam-si, , South Korea
Countries
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Central Contacts
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Facility Contacts
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InHo Chae
Role: primary
Other Identifiers
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AD-224P3
Identifier Type: -
Identifier Source: org_study_id
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