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The primary objectives of this study are to assess the safety of ABT-450/r/ABT-267 with and without ABT-333 coadministered with and without ribavirin (RBV) for 12 and 24 weeks in HCV GT1- or 4-infecte...
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Lead Sponsor
AbbVie
NCT06718530 · Hepatitis C Virus Infection
NCT06463912 · Hepatitis C Virus Infection
NCT06180590 · Chronic Hepatitis C, Medication Reaction
NCT05361603 · Hepatitis C, Transmission, Intravenous Drug Abuser, and more
NCT03993925 · Chronic Hepatitis C, Intravenous Drug Usage
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This clinical trial information is sourced from ClinicalTrials.gov, a service of the U.S. National Institutes of Health.
Modifications: This data has been reformatted for display purposes. Eligibility criteria have been parsed into inclusion/exclusion sections. Location data has been geocoded to enable distance-based search. For the authoritative and most current information, please visit ClinicalTrials.gov.
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