Trials / Completed
CompletedNCT05155995
A Study to Evaluate the Pharmacokinetics and Safety Between HCP2001 and Co-administration of Each Component in Healthy Volunteers
A Randomized, Open Label, Single Dose, 2-way Crossover Clinical Trial to Evaluate the Pharmacokinetic Characteristics and Safety Between After Administration of a Fixed-dose Combination Drug of HCP2001 and Co-administration of Each Component in Healthy Volunteers
- Status
- Completed
- Phase
- Phase 1
- Study type
- Interventional
- Enrollment
- 71 (actual)
- Sponsor
- Hanmi Pharmaceutical Company Limited · Industry
- Sex
- All
- Age
- 19 Years – 54 Years
- Healthy volunteers
- Accepted
Summary
The purpose of this study is to evaluate the pharmacokinetic characteristics and safety between HCP2001 and co-administration of each component in fasting and fed conditions respectively in healthy volunteers.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | HCP2001 | Take it once per period. |
| DRUG | RLD2007 | Take it once per period. |
| DRUG | RLD2008 | Take it once per period. |
| DRUG | RLD2102 | Take it once per period. |
Timeline
- Start date
- 2021-09-28
- Primary completion
- 2022-11-27
- Completion
- 2022-11-27
- First posted
- 2021-12-14
- Last updated
- 2023-09-22
Locations
1 site across 1 country: South Korea
Source: ClinicalTrials.gov record NCT05155995. Inclusion in this directory is not an endorsement.