A Study to Evaluate Long-term Outcomes Following Treatment With ABT-450/Ritonavir/ABT-267 (ABT-450/r/ABT-267) and ABT-333 With or Without Ribavirin (RBV) in Adults With Genotype 1 Chronic Hepatitis C Virus (HCV) Infection

Study Identifier
M14-423
CT.gov Identifier
EudraCT Identifier
EUCTIS ID
Not available
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Study Complete

Results Available

Protocol
Available Language(s): English
Statistical Analysis Plan
Available Language(s): English
Scientific Result Summary
Available Language(s): English
Plain Language Summary
Available Language(s): English, French, Dutch, Portuguese (Native), Italian, Turkish

Study Details

Medical Condition
  • Hepatitis
  • Study Drug
  • ABT-450/r/ABT-267
  • ABT-333
  • Ribavirin (RBV)
  • Phase
    Phase 3
    Sex
    Female & Male
    Age
    18 - 99 Years

    Protocol Summary

    The purpose of this study was to evaluate the effect of treatment with ABT-450 co-formulated with ritonavir and ABT-267 (ABT-450/r/ABT-267) and ABT-333; 3-DAA regimen, with or without ribavirin (RBV) in adults with chronic hepatitis C virus genotype 1 (HCV GT1) infection.

    Study Locations

    Location
    Status
    Location
    CHU Bab El Oued /ID# 145420
    Algiers, Algeria, 16000
    Status
    Not applicable
    Location
    CHU Bologhine Hospital /ID# 145421
    Algiers, Algeria, 16000
    Status
    Not applicable
    Location
    CHU Mustapha Bacha /ID# 132130
    Algiers, Algeria, 16000
    Status
    Not applicable
    Location
    St Vincent's Hospital Sydney /ID# 131001
    Darlinghurst, New South Wales, Australia, 2010
    Status
    Not applicable
    Location
    Nepean Hospital /ID# 130999
    Kingswood, New South Wales, Australia, 2747
    Status
    Not applicable
    Location
    Westmead Hospital /ID# 130997
    Westmead, New South Wales, Australia, 2145
    Status
    Not applicable
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