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CompletedNCT02897726

A Study to Evaluate the Safety and Pharmacokinetics of NVP-1402

A Clinical Trial to Evaluate the Pharmacokinetics and Safety of NVP-1402 in Healthy Male Subjects

Status
Completed
Phase
Phase 1
Study type
Interventional
Enrollment
38 (actual)
Sponsor
NVP Healthcare · Industry
Sex
Male
Age
19 Years
Healthy volunteers
Accepted

Summary

The purpose of this study is to evaluate and compare the safety and pharmacokinetics of NVP-1402 and NVP-1402R in healthy male subjects.

Detailed description

This study is designed as randomized, open-label, active-controlled and crossover assignment for evaluate and compare the safety and pharmacokinetics of NVP-1402 and NVP-1402R in healthy male subjects. The safety assessed through adverse events up to 17 days after administration. Additional variables (ECGs, laboratory test, vital signs, so on) will also be recorded and assessed.

Conditions

Interventions

TypeNameDescription
DRUGNVP-1402Oral
DRUGNVP-1402ROral

Timeline

Start date
2017-03-24
Primary completion
2017-07-03
Completion
2017-07-03
First posted
2016-09-13
Last updated
2017-08-08

Locations

1 site across 1 country: South Korea

Source: ClinicalTrials.gov record NCT02897726. Inclusion in this directory is not an endorsement.

A Study to Evaluate the Safety and Pharmacokinetics of NVP-1402 (NCT02897726) · Clinical Trials Directory