This Registry is designed to obtain long term data on subject who have failed to achieve
sustained virologic response (SVR) while receiving at least one Gilead oral antiviral agent
(OAV) in a previous Gilead-sponsored hepatitis C study.
Have previously participated in a Gilead-sponsored hepatitis C study and received at least one Gilead OAV;
Have failed to achieve an SVR in a previous Gilead-sponsored study, as defined in the original treatment protocol;
Have detectable DRMs results available from the previous Gilead-sponsored treatment protocol;
Provide written, informed consent
Be willing and able to comply with the visit schedule.
Subject plans to start a new course of hepatitis C therapy including any investigational drug or device during the course of the follow-up Registry.
History of clinically-significant illness or any other major medical disorder that may interfere with subject follow-up, assessments or compliance with the protocol.