This Registry is designed to obtain long term data on subject who have failed to achieve
sustained virologic response (SVR) while receiving at leas
- Trial ID:
- Paul Pockros
- 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;
- 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.