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Search / Trial NCT06291207

A Study to Evaluate the Efficacy and Safety of AD-224

Launched by ADDPHARMA INC. · Feb 27, 2024

Trial Information

Current as of July 23, 2025

Recruiting

Keywords

ClinConnect Summary

This clinical trial is studying a new treatment called AD-224 for people with essential hypertension, which is a common type of high blood pressure. The main goal of the study is to see how well AD-224 works and whether it is safe for patients. The trial is currently looking for participants who are aged 39 and older and who have been diagnosed with essential hypertension. To take part in the study, patients will need to provide their consent and meet specific health criteria.

Participants in this trial can expect to receive either the study drug or a placebo (a pill that looks like the real drug but has no active ingredients) to help researchers determine the effectiveness of AD-224. It is important to note that individuals with secondary hypertension, which is high blood pressure caused by another health issue, cannot participate. This study aims to gather valuable information that could help improve treatments for people living with high blood pressure.

Gender

ALL

Eligibility criteria

  • Inclusion Criteria:
  • Signed informed consent
  • Patients with Essential Hypertension
  • Other inclusions applied
  • Exclusion Criteria:
  • Patient with Secondary Hypertension
  • Other exclusions applied

About Addpharma Inc.

Addpharma Inc. is a biopharmaceutical company dedicated to advancing innovative therapies for unmet medical needs. With a focus on the development of novel treatments across various therapeutic areas, Addpharma leverages cutting-edge research and technology to enhance patient outcomes. Committed to rigorous clinical trial standards and ethical practices, the company collaborates with healthcare professionals and research institutions to ensure the safety and efficacy of its products. Addpharma Inc. aims to contribute to the global healthcare landscape by delivering breakthrough solutions that improve quality of life for patients worldwide.

Locations

Seongnam Si, , Korea, Republic Of

Patients applied

0 patients applied

Trial Officials

InHo Chae, M.D., Ph.D

Principal Investigator

Seoul National University Bundang Hospital

Timeline

First submit

Trial launched

Trial updated

Estimated completion

Not reported