Trials / Recruiting
RecruitingNCT06441630
A Study to Evaluate the Efficacy and Safety of Co-administration of AD-227A and AD-227B
A Multicenter, Randomized, Double-blind, Phase III Study to Evaluate the Efficacy and Safety of AD-227A and AD-227B Combination Treatment in Patients with Essential Hypertension
- Status
- Recruiting
- Phase
- Phase 3
- Study type
- Interventional
- Enrollment
- 251 (estimated)
- Sponsor
- Addpharma Inc. · Industry
- Sex
- All
- Age
- 19 Years
- Healthy volunteers
- Not accepted
Summary
The purpose of this study is to evaluate the efficacy and safety of co-administration of AD-227A and AD-227B in patients with essential hypertension
Detailed description
Essential Hypertension
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | AD-227A | Per Oral, 1 Tablet, Once a day for 8 weeks |
| DRUG | AD-227B | Per Oral, 1 Tablet, Once a day for 8 weeks |
| DRUG | AD-227C | Per Oral, 1 Tablet, Once a day for 8 weeks |
| DRUG | Placebo of AD-227B | Per Oral, 1 Tablet, Once a day for 8 weeks |
| DRUG | Placebo of AD-227C | Per Oral, 1 Tablet, Once a day for 8 weeks |
Timeline
- Start date
- 2024-07-31
- Primary completion
- 2025-09-01
- Completion
- 2025-09-01
- First posted
- 2024-06-04
- Last updated
- 2025-02-04
Locations
1 site across 1 country: South Korea
Source: ClinicalTrials.gov record NCT06441630. Inclusion in this directory is not an endorsement.