A Study to Evaluate the Efficacy and Safety of AD-218
Launched by ADDPHARMA INC. · May 27, 2022
Trial Information
Current as of June 26, 2025
Recruiting
Keywords
ClinConnect Summary
This clinical trial is studying a new treatment called AD-218 for people with mixed dyslipidemia, which is a condition that affects cholesterol and fat levels in the blood. The main goal is to see how well AD-218 works and if it is safe for patients. The trial is currently looking for participants who are at least 19 years old, and both men and women can join. Before taking part, you would need to sign a consent form to show that you understand the study.
If you decide to participate, you can expect to receive the treatment and be monitored by healthcare professionals throughout the trial. It's important to know that some individuals may not be eligible to join if they have certain health conditions, such as fibromyalgia or muscle disorders. Overall, this study aims to find a better way to manage mixed dyslipidemia and improve health outcomes for those affected.
Gender
ALL
Eligibility criteria
- Inclusion Criteria:
- • A man or woman over 19 years old.
- • Sign on ICF prior to study participation
- Exclusion Criteria:
- • History of Fibromyalgia, Myopathy etc (CK ≥ 2 X ULN)
- • 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.
Contacts
Jennifer Cobb
Immunology at National Institute of Allergy and Infectious Diseases (NIAID)
Locations
Daegu, Nam Gu, Korea, Republic Of
Patients applied
Trial Officials
Kyu Chang Won, M.D., Ph.D
Principal Investigator
Yeungnam University Hospital
Timeline
First submit
Trial launched
Trial updated
Estimated completion
Not reported
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