Trials / Recruiting
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
| Type | Name | Description |
|---|---|---|
| DRUG | AD-115A, AD-1151 | Single-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.