Clinical Trials Directory

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

TypeNameDescription
DRUGAD-227APer Oral, 1 Tablet, Once a day for 8 weeks
DRUGAD-227BPer Oral, 1 Tablet, Once a day for 8 weeks
DRUGAD-227CPer Oral, 1 Tablet, Once a day for 8 weeks
DRUGPlacebo of AD-227BPer Oral, 1 Tablet, Once a day for 8 weeks
DRUGPlacebo of AD-227CPer 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.