A Follow-up Assessment of Resistance to ABT-333 in Hepatitis C Virus (HCV)-Infected Subjects Who Have Received ABT-333 in ABT-333 Studies

Study Identifier
M10-459
CT.gov Identifier
NCT00726882
EudraCT Identifier
Not available
EUCTIS ID
Not available
For general inquiries, please contact

844-663-3742 or [email protected]

Study Complete

Results Available

Scientific Result Summary
Available Language(s): English
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Study Details

Medical Condition
  • Hepatitis
    • Study Drug
  • ABT-333
    • Phase
    Phase 2
    Sex
    Female & Male
    Age
    18 - 65 Years
    Inclusion and Exclusion Criteria
    Inclusion Criteria:
    \- Main Selection Criteria: Subject received ABT-333 or matching placebo in a prior clinical study involving ABT-333.
    Exclusion Criteria:
    \- The investigator considers the subject unsuitable for the study for any reasons inclusive of, but not limited to, failure to comply with study procedures in prior ABT-333 clinical study.

    Protocol Summary

    The purpose of this follow-up study is to evaluate the frequency and persistence of specific viral mutations in response to treatment with ABT-333 (dasabuvir).

    Study Locations

    Location
    Status
    Location
    Site Reference ID/Investigator# 17665
    Anaheim, California, United States, 92801
    Status
    Not applicable
    Location
    Site Reference ID/Investigator# 17367
    Los Angeles, California, United States, 90036
    Status
    Not applicable
    Location
    Site Reference ID/Investigator# 17672
    Los Angeles, California, United States, 90048
    Status
    Not applicable
    Location
    Site Reference ID/Investigator# 10381
    Orlando, Florida, United States, 32803
    Status
    Not applicable
    Location
    Site Reference ID/Investigator# 17667
    Baton Rouge, Louisiana, United States, 70808
    Status
    Not applicable
    Location
    Site Reference ID/Investigator# 14461
    San Antonio, Texas, United States, 78215
    Status
    Not applicable
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