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Not Yet RecruitingNCT06916169

A Study to Evaluate the Safety and Pharmacokinetics of AG2304 Compared to Coadministration of AG23041 and AG23042

An Open-label, Randomized, Fasting, Single, Group 2, Stage 2, Cross-over Study to Evaluate the Safety and Pharmacokinetics of AG2304 Compared to Coadministration of AG23041 and AG23042 in Healthy Adult Volunteers

Status
Not Yet Recruiting
Phase
Phase 1
Study type
Interventional
Enrollment
70 (estimated)
Sponsor
Ahn-Gook Pharmaceuticals Co.,Ltd · Industry
Sex
All
Age
19 Years – 65 Years
Healthy volunteers
Accepted

Summary

The objective of this study is to evaluate the pharmacokinetic characteristics of AG2304 in healthy subjects.

Detailed description

To evaluate the pharmacokinetic characteristics and safety profiles of AG2304 compared with coadministration AG23041 and AG23042 after a single oral dose administration in healthy Korean subjects under fasting conditions.

Conditions

Interventions

TypeNameDescription
DRUGAG2304AG2304, Single-dose Oral Administration
DRUGAG23041 and AG23042AG23041/AG23042, Single-dose Oral Administration

Timeline

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

Source: ClinicalTrials.gov record NCT06916169. Inclusion in this directory is not an endorsement.

A Study to Evaluate the Safety and Pharmacokinetics of AG2304 Compared to Coadministration of AG23041 and AG23042 (NCT06916169) · Clinical Trials Directory