Trials / Completed
CompletedNCT05062876
A Study to Compare PK, PD and Safety of the AD-214 and AD-2141
A Randomized, Open-label, Multiple-dose, Crossover Study to Compare the Safety, Pharmacokinetics and Pharmacodynamics of AD-214 to AD-2141 in Healthy Volunteers
- Status
- Completed
- Phase
- Phase 1
- Study type
- Interventional
- Enrollment
- 41 (actual)
- Sponsor
- Addpharma Inc. · Industry
- Sex
- All
- Age
- 19 Years – 50 Years
- Healthy volunteers
- Accepted
Summary
A study to compare safety, pharmacokinetics and pharmacodynamics of AD-214 to AD-2141 in healthy volunteers.
Detailed description
This study is to compare the safety, pharmacokinetic characteristics and pharmacodynamics characteristics of AD-214 compared with administration of AD-2141 in healthy volunteers.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | AD-214 | 1 tablet administered before the breakfast during 7 days |
| DRUG | AD-2141 | 1 tablet administered before the breakfast during 7 days |
Timeline
- Start date
- 2021-11-01
- Primary completion
- 2022-03-17
- Completion
- 2022-03-29
- First posted
- 2021-09-30
- Last updated
- 2022-07-20
Locations
1 site across 1 country: South Korea
Source: ClinicalTrials.gov record NCT05062876. Inclusion in this directory is not an endorsement.