A Registry for Adolescent and Pediatric Participants Who Received a Gilead Hepatitis C Virus Direct Acting Antiviral (DAA) in Gilead-Sponsored Chronic Hepatitis C Infection Trials

Inclusion Criteria:

- Have previously participated in a Gilead-sponsored chronic hepatitis C study as an
adolescent or pediatric participant and received at least one Gilead HCV direct acting
antiviral

- Parent or legal guardian able to provide written informed consent OR individual is
able to provide written informed consent prior to any study procedures and willing to
comply with study requirements as determined by institutional review board
(IRB)/independent ethics committee(IEC)/local requirements and Investigator's
discretion.

- Individual is able to provide written assent, if they have the ability to read and
write, as determined by IRB/IEC/local requirements and Investigator's discretion

Exclusion Criteria:

- Individual is currently receiving or plans to initiate 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 the individual's follow-up, assessments or compliance with the
protocol.