The purpose of this study is to determine if DV-601, an investigational, therapeutic vaccine will be well-tolerated and induce hepatitis B virus (HBV)-specific virological and immunological responses in chronic hepatitis B (CHB) patients.
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
TREATMENT
Masking
NONE
Enrollment
14
Collegium Medicum Uniwersytet im. Mikołaja Kopernika
Bydgoszcz, Poland
Samodzielny Publiczny Wojewódzki Szpital Zespolony
Szczecin, Poland
Wojewódzki Szpital Zakaźny
Warsaw, Poland
NZOZ Centrum Badan Klinicznych
Wroclaw, Poland
Patient diaries, adverse events, physical exams, and lab tests
Time frame: Through Day 99
HBV-DNA levels
Time frame: Change from baseline to Days 43 and 99, and to Weeks 24 and 48
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