A Study of Albuferon With Ribavirin in Interferon Treatment Experienced Subjects With Chronic Hepatitis C
NCT ID: NCT00097435
Last Updated: 2013-08-02
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
PHASE2
115 participants
INTERVENTIONAL
2004-10-31
2007-08-31
Brief Summary
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Detailed Description
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Conditions
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Study Design
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RANDOMIZED
PARALLEL
TREATMENT
NONE
Interventions
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Albuferon
Ribavirin
Eligibility Criteria
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Inclusion Criteria
* Have previously failed to respond to treatment with any interferon alfa (IFNa) product
* Have compensated liver disease with the following minimum criteria: white blood cell count \> 3,000/mm3, absolute neutrophil count (ANC) \> 2,000/mm3, platelets \> 125,000/mm3, and hemoglobin (Hb) \> 13 g/dL for males or \> 12 g/dL for females.
Exclusion Criteria
* Pregnant or lactating female.
* History of any other medical disease or condition that would make the subject (in the opinion of the investigator) unsuitable for the study.
* A current drug or alcohol addiction
18 Years
65 Years
ALL
No
Sponsors
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Human Genome Sciences Inc.
INDUSTRY
Responsible Party
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Principal Investigators
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GSK Clinical Trials
Role: STUDY_DIRECTOR
GlaxoSmithKline
Locations
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Mayo Clinic
Phoenix, Arizona, United States
University of Florida CRC
Gainesville, Florida, United States
University of Florida at Jacksonville
Jacksonville, Florida, United States
Mayo Clinic Jacksonville
Jacksonville, Florida, United States
Johns Hopkins University
Baltimore, Maryland, United States
Mayo Clinic Rochester
Rochester, Minnesota, United States
Duke University
Durham, North Carolina, United States
Metropolitan Research
Fairfax, Virginia, United States
Countries
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Other Identifiers
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Clinical Protocol ALFR-HC-05
Identifier Type: -
Identifier Source: org_study_id