This study is a multi-center, double-blind, active-controlled, randomized, parallel clinical study to evaluate the efficacy and safety of DA-2803 in chronic hepatitis B subjects
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
DOUBLE
Enrollment
120
The Catholic University of Korea, Seoul
Seoul, South Korea
HBV DNA(log10 IU/mL) change
HBV DNA(log10 IU/mL) change compared to baseline
Time frame: 48 weeks
This platform is for informational purposes only and does not constitute medical advice. Always consult a qualified healthcare professional.
All participants are administered one tablet per day for 48 weeks