Trials / Completed
CompletedNCT06289933
A Study to Compare the Pharmacokinetics and the Safety Between a Fixed-dose Combination Administration of "BR3005" and Co-administration of "BR3005-1" and "BR3005-2" Under Fed Conditions in Healthy Adult Volunteers
An Open Label, Randomized, Fed, Single Dose, 2-sequence, 2-period, Crossover Study to Compare the Pharmacokinetics and the Safety Between a Fixed-dose Combination Administration of "BR3005" and Co-administration of "BR3005-1" and "BR3005-2" in Healthy Adult Volunteers
- Status
- Completed
- Phase
- Phase 1
- Study type
- Interventional
- Enrollment
- 40 (actual)
- Sponsor
- Boryung Pharmaceutical Co., Ltd · Industry
- Sex
- All
- Age
- 19 Years
- Healthy volunteers
- Accepted
Summary
The objective of this clinical study is to compare the pharmacokinetics and the safety between a fixed-dose combination administration of "BR3005" and co-administration of "BR3005-1" and "BR3005-2" under fed conditions in healthy adult volunteers
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | BR3005 | One tablet administered alone, Once a day |
| DRUG | BR3005-1 | One tablet administered alone, Once a day |
| DRUG | BR3005-2 | One tablet administered alone, Once a day |
Timeline
- Start date
- 2024-03-05
- Primary completion
- 2024-04-03
- Completion
- 2024-04-03
- First posted
- 2024-03-04
- Last updated
- 2024-05-24
Locations
1 site across 1 country: South Korea
Source: ClinicalTrials.gov record NCT06289933. Inclusion in this directory is not an endorsement.