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Trial details imported from ClinicalTrials.gov
For full trial details, please see the original record at
https://clinicaltrials.gov/study/NCT00115908
Registration number
NCT00115908
Ethics application status
Date submitted
26/06/2005
Date registered
27/06/2005
Date last updated
7/11/2013
Titles & IDs
Public title
A Study of Albuferon and Ribavirin in Interferon Naive Subjects With Chronic Hepatitis C Genotype 1
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Scientific title
A Phase 2b, Randomized, Multi-Center, Active-Controlled, Open-Label Study to Evaluate the Efficacy and Safety of Albuferon (Recombinant Human Albumin-Interferon Alfa Fusion Protein) in Combination With Ribavirin in Interferon Alfa Naive Subjects With Chronic Hepatitis C Genotype 1
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Secondary ID [1]
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ALFR-HC-04
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Universal Trial Number (UTN)
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Trial acronym
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Linked study record
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Health condition
Health condition(s) or problem(s) studied:
Hepatitis C, Chronic
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Condition category
Condition code
Infection
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Other infectious diseases
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Oral and Gastrointestinal
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Other diseases of the mouth, teeth, oesophagus, digestive system including liver and colon
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Intervention/exposure
Study type
Interventional
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Description of intervention(s) / exposure
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Comparator / control treatment
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Control group
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Outcomes
Primary outcome [1]
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Sustained virologic response (SVR), defined as undetectable HCV RNA at 24 weeks after the end of therapy.
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Assessment method [1]
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Timepoint [1]
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Secondary outcome [1]
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Virologic response at Week 4 (VR4), defined as undetectable HCV RNA or a > 2-log reduction in HCV RNA.
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Assessment method [1]
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Timepoint [1]
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Secondary outcome [2]
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Early virologic response at Week 12 (EVR12), defined as undetectable HCV RNA or a > 2-log reduction in HCV RNA.
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Assessment method [2]
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Timepoint [2]
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Secondary outcome [3]
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Undetectable HCV RNA at Week 24.
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Assessment method [3]
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Timepoint [3]
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Secondary outcome [4]
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End of treatment response (ETR), defined as undetectable HCV RNA at Week 48
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Assessment method [4]
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Timepoint [4]
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Eligibility
Key inclusion criteria
Key
* Interferon treatment naive subjects with chronic hepatitis C, HCV genotype 1.
* Compensated liver disease
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Minimum age
18
Years
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Maximum age
65
Years
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Sex
Both males and females
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Can healthy volunteers participate?
No
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Key exclusion criteria
* Pregnant or lactating female or males with a pregnant partner.
* A positive test for serum antibodies to the human immunodeficiency virus (HIV-1) or serum hepatitis B virus surface antigen (HBsAg).
* A history of moderate, severe or uncontrolled psychiatric disease.
* A history of immunologically mediated disease, seizure disorder, chronic cardiac disease, chronic pulmonary disease, hemoglobinopathy, coagulopathy, or malignancy.
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Study design
Purpose of the study
Treatment
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Allocation to intervention
Randomised controlled trial
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Procedure for enrolling a subject and allocating the treatment (allocation concealment procedures)
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Methods used to generate the sequence in which subjects will be randomised (sequence generation)
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Masking / blinding
Open (masking not used)
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Who is / are masked / blinded?
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Intervention assignment
Parallel
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Other design features
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Phase
Phase 2
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Type of endpoint/s
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Statistical methods / analysis
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Recruitment
Recruitment status
Completed
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Data analysis
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Reason for early stopping/withdrawal
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Other reasons
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Date of first participant enrolment
Anticipated
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Actual
1/05/2005
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Date of last participant enrolment
Anticipated
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Actual
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Date of last data collection
Anticipated
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Actual
1/05/2007
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Sample size
Target
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Accrual to date
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Final
458
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Recruitment in Australia
Recruitment state(s)
NSW,QLD,SA,VIC,WA
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Recruitment hospital [1]
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Royal Prince Alfred Hospital - Camperdown
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Recruitment hospital [2]
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Concord Repatriation General Hospital - Concord
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John Hunter Hospital - New Lambton Heights
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Westmead Hospital - Westmead
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Princess Alexandra Hospital - Brisbane
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Royal Brisbane Hospital - Herston
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Royal Adelaide Hospital - Adelaide
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Monash Medical Centre - Clayton
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St. Vincents Hospital - East Melbourne
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Western Hospital - Footscray
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Austin Health - Heidelberg
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The Alfred - Melbourne
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Royal Melbourne Hospital - Melbourne
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Fremantle Hospital - Fremantle
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Sir Charles Gairdner Hospital - Nedlands
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Royal Perth Hospital - Perth
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Recruitment postcode(s) [1]
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2050 - Camperdown
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Recruitment postcode(s) [2]
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2139 - Concord
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2305 - New Lambton Heights
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2145 - Westmead
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Recruitment postcode(s) [5]
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4102 - Brisbane
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Recruitment postcode(s) [6]
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4029 - Herston
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Recruitment postcode(s) [7]
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5000 - Adelaide
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Recruitment postcode(s) [8]
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3168 - Clayton
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Recruitment postcode(s) [9]
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3002 - East Melbourne
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Recruitment postcode(s) [10]
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3011 - Footscray
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Recruitment postcode(s) [11]
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3081 - Heidelberg
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3004 - Melbourne
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Recruitment postcode(s) [13]
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3050 - Melbourne
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Recruitment postcode(s) [14]
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6160 - Fremantle
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Recruitment postcode(s) [15]
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6009 - Nedlands
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Recruitment postcode(s) [16]
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6000 - Perth
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Recruitment outside Australia
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Canada
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Alberta
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Brno
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Hradec Kralove
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Melnik
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Opava
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Prague
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Czech Republic
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Usti nad labem
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Nazareth
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Petah Tiqwa
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Cluj-Napoca
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Romania
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Iasi
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Funding & Sponsors
Primary sponsor type
Commercial sector/industry
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Name
Human Genome Sciences Inc.
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Address
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Ethics approval
Ethics application status
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Summary
Brief summary
The purpose of the study is to evaluate the efficacy and safety of Albuferon in combination with ribavirin in interferon (IFN) alfa treatment-naïve subjects with chronic hepatitis C genotype 1. The study will randomize subjects to 1 of 4 treatment groups including 3 different Albuferon groups or to the active control group, peginterferon alfa-2a (PEGASYS, PEG-IFNalfa-2a). All subjects will also receive oral daily ribavirin.
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Trial website
https://clinicaltrials.gov/study/NCT00115908
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Trial related presentations / publications
Neumann AU, Pianko S, Zeuzem S, Yoshida EM, Benhamou Y, Mishan M, McHutchison JG, Pulkstenis E, Mani Subramanian G. Positive and negative prediction of sustained virologic response at weeks 2 and 4 of treatment with albinterferon alfa-2b or peginterferon alfa-2a in treatment-naive patients with genotype 1, chronic hepatitis C. J Hepatol. 2009 Jul;51(1):21-8. doi: 10.1016/j.jhep.2009.01.017. Epub 2009 Mar 11. Zeuzem S, Yoshida EM, Benhamou Y, Pianko S, Bain VG, Shouval D, Flisiak R, Rehak V, Grigorescu M, Kaita K, Cronin PW, Pulkstenis E, Subramanian GM, McHutchison JG. Albinterferon alfa-2b dosed every two or four weeks in interferon-naive patients with genotype 1 chronic hepatitis C. Hepatology. 2008 Aug;48(2):407-17. doi: 10.1002/hep.22403.
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Public notes
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Contacts
Principal investigator
Name
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GSK Clinical Trials
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Address
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GlaxoSmithKline
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Contact person for scientific queries
No information has been provided regarding IPD availability
What supporting documents are/will be available?
No Supporting Document Provided
Results publications and other study-related documents
No documents have been uploaded by study researchers.
Results not provided in
https://clinicaltrials.gov/study/NCT00115908
Download to PDF