Clinical Trials Directory

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

TypeNameDescription
DRUGNVP-1805orally, once daily on Period 1 and Period 3 (or Period 2 and Period 4) (NVP-1805 80/10/20.8mg)
DRUGNVP-1805-R1and NVP-1805-R2orally, 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.

NVP-1805 Compared to Coadministration of NVP-1805-R1 With NVP-1805-R2 in Healthy Adult Volunteers (NCT04905342) · Clinical Trials Directory