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Clinical trialNCT04237376UnknownObservational

Chronic HBV Infection in Pregnant Women Taking TAF to Prevent Vertical Transmission

SponsorNew Discovery LLCEnrollment600Hepatitis B, ChronicPregnancy Related
View the registry record on ClinicalTrials.gov

Summary

The lay summary the sponsor registered on ClinicalTrials.gov.

Mother-to-child transmission is the main route of transmission of Hepatitis B Virus (HBV) in China, and about 30% - 50% of chronic HBV carriers are infected by this. Although the current hepatitis B vaccine combined with hepatitis B immunoglobulin scheme has achieved excellent results, about 5% - 10% of infants born to chronic hepatitis B (CHB) mothers are still infected. A pregnant women's blood hepatitis B virus load ≥ 2 × 10\^5 IU/mL before delivery is the main risk factor for transmission prevention failure. Two recent random controlled trial (RCT) studies have shown that the use of Tenofovir Disoproxil Fumarate (TDF) in highly viremic HBsAg positive mothers may safely reduce the rate of MTCT in comparisons between groups of TDF treated and untreated patients. Tenofovir Alafenamide (TAF) is the successor to TDF, and both drugs have a similar mechanism of action to reduce HBV DNA levels and normalize serum alanine aminotransferase (ALT) in chronic hepatitis B patients (CHB). TAF however, has a better safety profile with less adverse effects to hip and spine bone mineral density and renal function. Currently, TAF has been approved by the State Food and Drug Administration and marketed in China in December 2018. On the drug label, it has been suggested that TAF may be considered during pregnancy if necessary. However, it has not been reported whether the application of TAF in pregnant women can achieve better effects and safety in prevention of mother-to-child transmission. This prospective, triple arm, multicenter study seeks to evaluate the efficacy and safety of TAF in the prevention of mother-to-child transmission as compared to a retrospective cohort of mothers who were treated with TDF.

Investigators

The overall officials registered on this study. Names that resolve to a findmyKOL profile link to it; the rest are shown as registered.

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Sites

4 registered facilities, with the per-site recruitment status where the registry publishes one. ClinicalTrials.gov does not publish per-site enrollment counts.

China
  • Beijing You'An Hospital, Capital Medical University

    Beijing, Beijing Municipality, China

    Yu Chen, MDYunxia Zhu, MD
    Recruiting
  • the Third Hospital of Qinhuangdao City

    Qinhuangdao, Hebei, China

    Lihua Cao, MDPeili Zhao, MD
    Recruiting
  • Department of Infectious Disease,the Fourth Affiliated Hospital of Harbin Medical University

    Harbin, Heilongjiang, China

    Lihua Zhong, MDLiying Zhu, MD
    Recruiting
  • Tongliao Infectious Disease Hospital

    Tongliao, Inner Mongolia, China

    Baiyila Han, MDDongmei Wei, MDShuyi Suo, MD
    Recruiting

Site investigator names are published by ClinicalTrials.gov only while a study recruits, so completed studies list sites without them.

Drugs studied

The drug and biological interventions registered on this study, normalized to their RxNorm ingredient where possible.

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Registration & key dates

Registry attributes as recorded on the ClinicalTrials.gov study record.

Start
9 Apr 2019
Primary completion
30 Sept 2020
Completion
30 Sept 2020
Last update posted
23 Jan 2020
Registered enrollment
600
Registry id
NCT04237376

Source: ClinicalTrials.gov, via the CTTI AACT database, data as of 24 Aug 2026. Registry facts are shown as registered by the study sponsor; findmyKOL does not interpret them.