Trials / Completed
CompletedNCT04905342
NVP-1805 Compared to Coadministration of NVP-1805-R1 With NVP-1805-R2 in Healthy Adult Volunteers
An Open-label, Randomized, Evaluate the Pharmacokinetics and the Safety of NVP-1805 Compared to Coadministration of NVP-1805-R1 With NVP-1805-R2 in Healthy Adult Volunteers
- Status
- Completed
- Phase
- Phase 1
- Study type
- Interventional
- Enrollment
- 58 (actual)
- Sponsor
- NVP Healthcare · Industry
- Sex
- All
- Age
- 19 Years
- Healthy volunteers
- Accepted
Summary
The purpose of this study is to compare the pharmacokinetics of NVP-1805 and coadministration of NVP-1805-R1 with NVP-1805-R2.
Detailed description
Evaluate pharmacokinetics and safety of NVP-1805 compared to coadministration of NVP-1805-R1 with NVP-1805-R2
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | NVP-1805 | orally, once daily on Period 1 and Period 3 (or Period 2 and Period 4) (NVP-1805 80/10/20.8mg) |
| DRUG | NVP-1805-R1and NVP-1805-R2 | orally, once daily on Period 1 or Period 3 (or Period 2 and Period 4) (NVP-1805-R1 80mg, NVP-1805-R2 10/20.8mg) |
Timeline
- Start date
- 2021-08-14
- Primary completion
- 2021-12-20
- Completion
- 2022-01-07
- First posted
- 2021-05-27
- Last updated
- 2022-02-11
Locations
1 site across 1 country: South Korea
Source: ClinicalTrials.gov record NCT04905342. Inclusion in this directory is not an endorsement.