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Prevention of Graft Reinfection After Liver Transplantation With Anti HCV Monoclonal Antibodies Identified in Chronically Infected Patients or in Patients With Resolved Hepatitis C

Prevention of Graft Reinfection After Liver Transplantation for HCV Related End-stage Liver Disease . Study of Humoral Anti-HCV Response

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT00638144
Enrollment
300
Registered
2008-03-18
Start date
2008-02-29
Completion date
2015-12-31
Last updated
2015-09-30

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Hepatitis C

Keywords

Hepatitis C, liver transplantation, antibodies mediated neutralization, monoclonal antibodies

Brief summary

End stage HCV-related cirrhosis has become a major indication for liver transplantation (LT). Unfortunately, recurrence of HCV infection on the liver graft occurs in almost all patients following transplantation and causes a persistent infection that leads to chronic hepatitis and cirrhosis in a significant proportion of patients. To date there is no effective way to prevent HCV reinfection of the liver graft in the early phase after transplantation. . Early passive immunotherapy with neutralizing antibodies against HCV should be considered for preventing reinfection of liver transplanted patients associated with HCV. This approach is well established in the case of patients undergoing liver transplantation for chronic hepatitis B virus infection. Our purpose is to produce neutralizing monoclonal antibodies to prevent reinfection of the liver graft.

Interventions

None listed

Sponsors

University Hospital, Strasbourg, France
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to 75 Years
Healthy volunteers
No

Inclusion criteria

* Health insurance * Resolved HCV infection ( HCV RNA negative since more then 6 months ) -HCV chronically infected ( RNA positive ) * Anti- HCV antibodies positive * Volunteers and informed patients

Exclusion criteria

* Immunosuppression * HBV or HIV infection * Pregnancy * Breast feeding

Countries

France

Contacts

Primary ContactBAUMERT Thomas, MD
thomas.baumert@chru-strasbourg.fr00 333 90 24 36 99
Backup ContactFrançoise STOLL-KELLER, MD
francoise.stoll@viro-ulp.u-strasbg.fr00 333 90 24 37 16

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026