Clinical Trial: A Long Term Follow-up Study of Patients From the REP 301 Protocol

Study Status: Active, not recruiting
Recruit Status: Active, not recruiting
Study Type: Observational

Official Title: A Long Term Follow-up Study of Patients From the REP 301 Protocol

Brief Summary: The REP 301 treatment protocol involved the treatment of patients with chronic hepatitis B / hepatitis D co-infection with two agents: REP 2139-Ca and pegylated interferon (peg-IFN). In this protocol, similar reduction/clearance of serum HBsAg and improved response to immunotherapy were observed in addition to clearance of serum HDV RNA. The REP 301 protocol was designed to include a 24 week follow-up period after treatment, however given the strong antiviral response against HBV and HDV infection in these patients, it is now important to extend the follow-up period in these patients to monitor over a longer period after treatment the safety and efficacy combined REP 2139-Ca / peg-IFN treatment in patients in the REP 301 protocol.

Detailed Summary: The REP 301-LTF is a long-term follow-up, non-blinded study of patients from the REP 301 protocol. In this study, all eligible patients from the REP 301 protocol will have their followup evaluation extended for an additional 3 years, consisting of 6 visits scheduled every 6 months following the last follow-up visit scheduled in the REP 301 protocol. During each visit a physical examination and documentation of any symptoms, experiences will be conducted as well as blood tests for safety and virology as described below. This study will examine the long term safety effects in patients who have completed of treatment exposure in the REP 301 trial (REP 2139-Ca therapy for 30 weeks and PEG-IFN taken for 48 weeks with a 15 week overlap in combination) and the duration of suppression of serum HBV and HDV viremia observed in the REP 301 protocol. This requires that subjects have completed antiviral treatment in the REP 301 protocol and are not immediately transitioned to further antiviral treatment unless necessary. The total duration of this study for each subject is 3 years.
Sponsor: Replicor Inc.

Current Primary Outcome:

  • Long term safety (test abnormalities) [ Time Frame: 3 years ]
    The proportion of patients with emergent lab test abnormalities.
  • Long term safety (AEs) [ Time Frame: 3 years ]
    Proportion of patients with adverse events.
  • Long term safety (SAEs) [ Time Frame: 3 years ]
    Proportion of patients with serious adverse events.


Original Primary Outcome: Same as current

Current Secondary Outcome:

  • Long term efficacy (serum HBsAg) [ Time Frame: 3 years ]
    Proportion of patients who maintain serum HBsAg < 1 IU/ml.
  • Long term efficacy (serum anti-HBs) [ Time Frame: 3 years ]
    Proportion of subjects who maintain anti-HBs titers above 10 mIU/ml.
  • Long term efficacy (serum HBV DNA) [ Time Frame: 3 years ]
    Proportion of patients who maintain serum HBV DNA < 10 IU / ml.
  • Long term efficacy (serum HDV RNA) [ Time Frame: 3 years ]
    Proportion of patients who maintain undetectable serum HDV RNA (target not detected).


Original Secondary Outcome: Same as current

Information By: Replicor Inc.

Dates:
Date Received: August 16, 2016
Date Started: August 2016
Date Completion: November 2019
Last Updated: February 6, 2017
Last Verified: February 2017