Clinical Trial:

Hep C Gilead registry (no SVR)

Full Name

Hepatitis C Registry (GS-US-248-0123): A long term follow-up registry study of subjects who did not achieve sustained virologic response in Gilead-sponsored trials in subjects with chronic hepatitis C infection (2_PRO00000638)

Description

This Registry study will enroll subjects who did not achieve a sustained virologic response after receiving at least one oral antiviral agent (OAV) while participating in a Gilead-sponsored hepatitis C clinical trial. For this current trial, patients who complete treatment with GS-7977 and fail to achieve a sustained virologic response, as defined by the protocol, will be asked to provide ongoing follow-up for three additional years. Once enrolled, participants will be followed for up to 3 years. Visits will occur at Baseline and Weeks 24, 48, 72, 96, 120 and 144. At each visit, subjects will have blood drawn and a quality of life survey will be completed.

Eligibility

Inclusion Criteria
  • Willing and able to provide written informed consent
  • Previously participated in a Gilead-sponsored study, received at least one Gilead oral antiviral, and failed to achieve a sustained virologic response
  • Able to comply with visit schedule and protocol requirements
  • Cannot be on any Hep C treatment course during study
Doctor(s) Running This Study