Trials / Completed
CompletedNCT04218552
Determining the Optimal Dose of AD-209 in Patients With Essential Hypertension
A Randomized, Double-Blind, Parallel, Multi-Center, Phase 2 Clinical Trial to Determine the Optimal Dose of AD-209 in Patients With Essential Hypertension
- Status
- Completed
- Phase
- Phase 2
- Study type
- Interventional
- Enrollment
- 176 (actual)
- Sponsor
- Addpharma Inc. · Industry
- Sex
- All
- Age
- 19 Years – 74 Years
- Healthy volunteers
- Not accepted
Summary
The purpose of this study is to determine the optimal dose of AD-209 in patients with Essential Hypertension.
Detailed description
Condition or disease : hypertension Intervention/treatment Drug : AD-209-H Drug : AD-209-M Drug : AD-209-L Drug : Placebo Drug : Amlodipine Drug : Telmisartan Phase : Phase 2
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | AD209 | PO, Once daily(QD), 8weeks |
| DRUG | Amlodipine low | PO, Once daily(QD), 8weeks |
| DRUG | Amlodipine high | PO, Once daily(QD), 8weeks |
| DRUG | Telmisartan | PO, Once daily(QD), 8weeks |
Timeline
- Start date
- 2020-02-25
- Primary completion
- 2021-02-25
- Completion
- 2021-02-25
- First posted
- 2020-01-06
- Last updated
- 2021-07-21
Locations
1 site across 1 country: South Korea
Source: ClinicalTrials.gov record NCT04218552. Inclusion in this directory is not an endorsement.