Hypertension,Essential Clinical Trial
Official title:
A Multicenter, Randomized, Double-blind, Active-control, Phase III Study to Evaluate the Efficacy and Safety of AD-223A and AD-223B Combination Therapy in Patients With Essential Hypertension
The purpose of this study is to evaluate the efficacy and safety of AD-223
| Status | Recruiting |
| Enrollment | 486 |
| Est. completion date | February 2025 |
| Est. primary completion date | February 2025 |
| Accepts healthy volunteers | No |
| Gender | All |
| Age group | 19 Years and older |
| Eligibility | Inclusion Criteria: - Signed informed consent - Other inclusions applied Exclusion Criteria: - Orthostatic hypotension with symptom - Other exclusions applied |
| Country | Name | City | State |
|---|---|---|---|
| Korea, Republic of | Hanyang University Hospital | Seoul |
| Lead Sponsor | Collaborator |
|---|---|
| Addpharma Inc. |
Korea, Republic of,
| Type | Measure | Description | Time frame | Safety issue |
|---|---|---|---|---|
| Primary | Change rate of MSSBP | Change from baseline in mean sitting systolic blood pressure | Baseline, Week 8 |
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