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Safety and Pharmacokinetic Characteristics of HD203 Liquid in Healthy Male Volunteers

NCT01894412 · Status: COMPLETED · Phase: PHASE1 · Type: INTERVENTIONAL · Enrollment: 48

Last updated 2016-07-14

No results posted yet for this study

Summary

The purpose of this study is to compare the safety and pharmacokinetic characteristics of HD203 liquid with those of etanercept (enbrel) prefilled injection after subcutaneous injection

Conditions

  • Healthy

Interventions

BIOLOGICAL

Etanercept (Enbrel)

BIOLOGICAL

HD203

Sponsors & Collaborators

  • Hanwha Chemical

    lead INDUSTRY

Principal Investigators

  • Kyung-Sang Yu · Seoul National University Hospital

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
QUADRUPLE
Model
CROSSOVER

Eligibility

Min Age
20 Years
Max Age
40 Years
Sex
MALE
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2013-07-31
Primary Completion
2015-12-31
Completion
2015-12-31

Countries

  • South Korea

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT01894412 on ClinicalTrials.gov