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RecruitingNCT07385235

Compare and Evaluate the Safety and PK Data of a Single Dose Administration of 'AD-115A' or 'AD-1151'

A Randomized, Open-label, Single-dose, Two-sequence, and Two-period Crossover Study to Evaluate the Pharmacokinetics and Safety Between the Administration of AD-115A and the Administration of AD-1151 for Healthy Subjects in Fasting State

Status
Recruiting
Phase
Phase 1
Study type
Interventional
Enrollment
46 (estimated)
Sponsor
Addpharma Inc. · Industry
Sex
All
Age
19 Years
Healthy volunteers
Not accepted

Summary

The study compare and evaluate the safety and pharmacokinetic characteristics of a single dose administration of 'AD-115A' or 'AD-1151' in healthy adults.

Detailed description

A randomized, open-label, single-dose, two-sequence, and two-period crossover study to evaluate the pharmacokinetics and safety between the administration of AD-115A and the administration of AD-1151 for healthy subjects in fasting state

Conditions

Interventions

TypeNameDescription
DRUGAD-115A, AD-1151Single-dose oral administration of AD-115A or AD-1151 (200 mg tablet), according to randomized sequence.

Timeline

Start date
2026-01-27
Primary completion
2026-03-07
Completion
2026-03-16
First posted
2026-02-04
Last updated
2026-02-11

Locations

1 site across 1 country: South Korea

Source: ClinicalTrials.gov record NCT07385235. Inclusion in this directory is not an endorsement.

Compare and Evaluate the Safety and PK Data of a Single Dose Administration of 'AD-115A' or 'AD-1151' (NCT07385235) · Clinical Trials Directory