Objectives: Primary Objective: To identify and preselect patients with chronic HBV mono infection, who are undetectable for anti-Ad5 nAb, currently being treated with nucleo(t)sides, for participation in the TG1050.02 Phase1/1b First in Man (FIM) study. Secondary Objectives: To assess the prevalence of undetectable anti-Ad5 nAb in chronic HBV mono-infected patients. Methodology: Patients with chronic HBV mono-infection, who are currently being treated with nucleo(t)sides for their HBV infection, will be enrolled in this study to measure Ad5 nAb levels. A single peripheral blood collection (4 mL) will be obtained and Ad5 nAb titers will be measured by a central laboratory using a newly validated assay.
Study Type
INTERVENTIONAL
Purpose
SCREENING
Enrollment
166
Unnamed facility
Montreal, Canada
Unnamed facility
Grenoble, France
Unnamed facility
Lyon, France
Unnamed facility
Nancy, France
Unnamed facility
Paris, France
Unnamed facility
Strasbourg, France
Unnamed facility
Freiburg im Breisgau, Germany
Unnamed facility
Hamburg, Germany
Unnamed facility
Hanover, Germany
Unnamed facility
Mainz, Germany
...and 1 more locations
Immunology analysis: Serum titers of Adenovirus serotypes 5 (Ad5) neutralizing antibodies (nAb)
Time frame: Day 1
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