Clinical Trials Directory

Trials / Unknown

UnknownNCT02580006

To Investigate the Pharmacokinetics of EPORON® and EPREX® After Subcutaneous Administration in Healthy Male Volunteers

A Randomized, Double-blind, Active Control, Single Dosing, Crossover Clinical Trial to Investigate the Pharmacokinetics of EPORON® and EPREX® After Subcutaneous Administration in Healthy Male Volunteers

Status
Unknown
Phase
Phase 1
Study type
Interventional
Enrollment
42 (estimated)
Sponsor
Dong-A ST Co., Ltd. · Industry
Sex
Male
Age
19 Years – 50 Years
Healthy volunteers
Accepted

Summary

This Phase I study is to compare pharmacokinetics, safety and pharmacodynamics of EPORON and EPREX after single subcutaneous administration.

Conditions

Interventions

TypeNameDescription
DRUGEPORONsingle dose administration subcutaneously
DRUGEPREXsingle dose administration subcutaneously

Timeline

Start date
2015-11-01
Primary completion
2016-01-01
Completion
2016-03-01
First posted
2015-10-20
Last updated
2015-10-20

Locations

1 site across 1 country: South Korea

Source: ClinicalTrials.gov record NCT02580006. Inclusion in this directory is not an endorsement.

To Investigate the Pharmacokinetics of EPORON® and EPREX® After Subcutaneous Administration in Healthy Male Volunteers (NCT02580006) · Clinical Trials Directory