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NOT YET RECRUITING
NCT06916130
PHASE1

A Study to Compare PK/PD Characteristics and Safety Profiles Between AD-120 and AD-120A

Sponsor: Addpharma Inc.

View on ClinicalTrials.gov

Summary

Primary endpoint of this study is to evaluate the pharmacokinetic and pharmacodynamic characteristics of AD-120 in healthy subjects.

Official title: A Randomized, Open-label, Multiple Oral-dose, 2x2 Crossover Clinical Trial to Compare the Safety, Pharmacokinetic, and Pharmacodynamic Characteristics of a AD-120 and AD-120A in Healthy Adult Volunteers

Key Details

Gender

All

Age Range

19 Years - 50 Years

Study Type

INTERVENTIONAL

Enrollment

48

Start Date

2025-04-21

Completion Date

2025-09-01

Last Updated

2025-04-08

Healthy Volunteers

Yes

Interventions

DRUG

AD-120A

Administered before the breakfast during 7 days, Oral, Tablet

DRUG

AD-120

Administered before the breakfast during 7 days, Oral, Tablet

Locations (1)

Seoul National University Hospital

Seoul, South Korea