Efficacy and Safety of Recombinant Factor VIII (GreenGene) in Patients With Hemophilia A
NCT01568580 · Status: COMPLETED · Phase: PHASE3 · Type: INTERVENTIONAL · Enrollment: 71
Last updated 2012-04-02
Summary
The purpose of this study is to study the evaluation of efficacy and safety of GreenGene (Recombinant Factor VIII).
Conditions
Interventions
- DRUG
-
GreenGene
Dose : 10 \~ 50IU/kg Administration method : intravenous infusion or bolus
Sponsors & Collaborators
-
Green Cross Corporation
lead INDUSTRY
Study Design
- Allocation
- NA
- Purpose
- TREATMENT
- Masking
- NONE
- Model
- SINGLE_GROUP
Eligibility
- Min Age
- 12 Years
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2004-12-31
- Primary Completion
- 2006-09-30
- Completion
- 2006-09-30
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