A Study to Compare to PK Characteristics and Safety Profiles Between AD-117 and AD-117A
NCT07152873 · Status: NOT_YET_RECRUITING · Phase: PHASE1 · Type: INTERVENTIONAL · Enrollment: 60
Last updated 2025-12-04
Summary
Primary endpoint of this study is to evaluate the pharmacokinetic characteristics of AD-117 in healthy subjects.
Conditions
- Mixed Dyslipidemia
Interventions
- DRUG
-
AD-117
AD-117 1Tab., Per Oral
- DRUG
-
AD-117A
AD-117A 1Tab., Per Oral
Sponsors & Collaborators
-
Addpharma Inc.
lead INDUSTRY
Study Design
- Allocation
- RANDOMIZED
- Purpose
- TREATMENT
- Masking
- NONE
- Model
- CROSSOVER
Eligibility
- Min Age
- 19 Years
- Sex
- ALL
- Healthy Volunteers
- Yes
Timeline & Regulatory
- Start
- 2025-12-01
- Primary Completion
- 2026-02-28
- Completion
- 2026-03-31
Countries
- South Korea
Study Locations
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