A Study to Evaluate the Efficacy and Safety of AD-218

Recruiting Phase 3 Interventional Study
Mixed Dyslipidemia
No Placebo Group Every participant receives an active treatment — no one gets a placebo. Pivotal Trial This treatment is in the last trial phase before FDA approval. Prior Safety Data This treatment has already been tested in at least one earlier human trial.
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At a Glance
Age
19 and older
Sex
Any
Trial phase
Phase 3
Study type
Interventional
Purpose
Treatment
Participants needed
520 (estimated)
Sponsor
Addpharma Inc. · Industry
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About This Trial

The purpose of this study is to evaluate the efficacy and safety of AD-218

Trial Locations
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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
Contacts

Sarah Yoon

82-031-891-5576

sryoon@addpharma.co.kr

CONTACT

Kyu Chang Won, M.D., Ph.D

CONTACT