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Not Yet RecruitingNCT06916130

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

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

Status
Not Yet Recruiting
Phase
Phase 1
Study type
Interventional
Enrollment
48 (estimated)
Sponsor
Addpharma Inc. · Industry
Sex
All
Age
19 Years – 50 Years
Healthy volunteers
Accepted

Summary

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

Detailed description

The purpose of this study is to evaluate the pharmacokinetic and pharmacodynamic characteristics and safety profiles of AD-120 compared with AD-120A in healthy subjects.

Conditions

Interventions

TypeNameDescription
DRUGAD-120AAdministered before the breakfast during 7 days, Oral, Tablet
DRUGAD-120Administered before the breakfast during 7 days, Oral, Tablet

Timeline

Start date
2025-04-21
Primary completion
2025-09-01
Completion
2025-09-01
First posted
2025-04-08
Last updated
2025-04-08

Locations

1 site across 1 country: South Korea

Source: ClinicalTrials.gov record NCT06916130. Inclusion in this directory is not an endorsement.

A Study to Compare PK/PD Characteristics and Safety Profiles Between AD-120 and AD-120A (NCT06916130) · Clinical Trials Directory