Hepatitis C Clinical Trial
Official title:
A Phase I Study to Assess the Safety and Immunogenicity of Ad6NSmut and AdCh3NSmut in Patients With Hepatitis C Virus Infection
HCV002TV is a Phase I study to ascertain the safety and immunogenicity of a novel vaccine
against Hepatitis C virus (HCV) in chronically infected patients. The vaccine is based on
the sequential delivery, by intramuscular route, of two different adenoviral vectors, of
chimpanzee and human origin respectively, bearing the same genetic information for HCV
antigens (NS region).
The two recombinant vaccine vectors, called AdCh3NSmut and Ad6NSmut, are weakened and unable
to multiply within the body; they are designed to induce an immune response against HCV
proteins. AdCh3NSmut and Ad6NSmut are being used in the ongoing HCV001 study in healthy
volunteers with very good safety and immunogenicity results.
HCV002TV is a dose-escalation study; the AdCh3NSmut is administered as priming vaccination
and Ad6NSmut as boosting vaccination.
The trial includes:
- Arm A, in which vaccinated patients are into Interferon-ribavirin therapy (the gold
standard therapy for hepatitis C);
- Arm B, in which vaccinated patients are not into therapy.
n/a
Allocation: Non-Randomized, Endpoint Classification: Safety Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Treatment
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