RecruitingPhase 3NCT06348576

Phase III Study to Evaluate the Efficacy and Safety of AD-209

A Multicenter, Randomized, Double-blind, Active-control, Phase III Study to Evaluate the Efficacy and Safety of AD-209 in Patients With Essential Hypertension


Sponsor

Addpharma Inc.

Enrollment

280 participants

Start Date

May 20, 2024

Study Type

INTERVENTIONAL

Conditions

Summary

The purpose of this study is to evaluate the efficacy and safety of AD-209


Eligibility

Min Age: 19 Years

Plain Language Summary

Simplified for easier understanding

This Phase III trial evaluates the effectiveness and safety of AD-209, a new medication, in a large group of patients. Details about the specific disease and drug mechanism are not fully disclosed in the public registry, but the study follows strict Phase III standards to confirm whether the drug works well enough to support approval. **You may be eligible if...** - You are able to provide signed informed consent - You meet the study's additional inclusion criteria (to be assessed by your doctor) **You may NOT be eligible if...** - You experience orthostatic hypotension with symptoms (dizziness or fainting when standing up) - You meet any of the study's other exclusion criteria (to be reviewed with your doctor) Talk to your doctor to see if this trial is right for you.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

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Interventions

DRUGAD-209

PO, Once daily(QD), 8weeks

DRUGAD-2091

PO, Once daily(QD), 8weeks

DRUGAD-209 Placebo

PO, Once daily(QD), 8weeks

DRUGAD-2091 Placebo

PO, Once daily(QD), 8weeks


Locations(1)

Korea University Guro Hospital

Seoul, South Korea

View Full Details on ClinicalTrials.gov

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NCT06348576


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