Safety and Pharmacokinetic Characteristics of HD203 Liq. in Healthy Subjects
NCT ID: NCT01431404
Last Updated: 2013-07-08
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
PHASE1
44 participants
INTERVENTIONAL
2011-08-31
2013-06-30
Brief Summary
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Detailed Description
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Conditions
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Study Design
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RANDOMIZED
CROSSOVER
TREATMENT
QUADRUPLE
Study Groups
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Enbrel, prefilled syringe
Etanercept (Enbrel)
prefilled syringe, SC
HD203, prefilled syringe
HD203
HD203, prefilled syringe, SC injection
Interventions
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Etanercept (Enbrel)
prefilled syringe, SC
HD203
HD203, prefilled syringe, SC injection
Eligibility Criteria
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Inclusion Criteria
* Weight over 55kg
* Subject who signed on ICF
Exclusion Criteria
20 Years
40 Years
MALE
Yes
Sponsors
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Hanwha Chemical
INDUSTRY
Responsible Party
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Principal Investigators
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Kyung-Sang Yu, M.D., Ph.D.
Role: PRINCIPAL_INVESTIGATOR
Seoul National University Hospital
Locations
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Seoul National University Hospital
Seoul, , South Korea
Countries
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Other Identifiers
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EAGLE-I-11
Identifier Type: -
Identifier Source: org_study_id
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