The purpose of this study is to evaluate the pharmacokinetics, efficacy and safety of TAF in HBV-infected pregnant women.
See this in plain English?
AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.
Assessment on the pharmacokinetics of TAF and TFV in plasma of pregnant women
Timeframe: The day before delivery
Rate of mother-to-child transmission of HBV
Timeframe: During 7-12 months after birth
Rate of birth defect of infants
Timeframe: From the date of birth to age of 28 weeks