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Tenofovir in Early Pregnancy to Prevent Mother-to-child Transmission of Hepatitis B Virus

Primary Purpose

Hepatitis B

Status
Completed
Phase
Phase 1
Locations
Thailand
Study Type
Interventional
Intervention
Tenofovir Disoproxil Fumarate
Sponsored by
Johns Hopkins Bloomberg School of Public Health
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Hepatitis B focused on measuring mother to child transmission, hepatitis B, tenofovir

Eligibility Criteria

16 Years - 49 Years (Child, Adult)FemaleDoes not accept healthy volunteers

Inclusion Criteria:

  • Pregnant women aged 18 and over
  • HBsAg positive
  • In the 12th-20th week of pregnancy
  • Willing to take TDF daily during pregnancy
  • Providing written informed consent
  • Plans to deliver at Shoklo Malaria Research Unit (SMRU)
  • Able and willing to comply with study requirements

Exclusion Criteria:

  • Anti-HIV positive
  • Negative qualitative HBV DNA if HBeAg negative
  • On immunosuppressive therapy
  • Elevated creatinine
  • History of kidney disease
  • Short cervix
  • History of pregnancy complications or prior pre-term labor

Sites / Locations

  • Shoklo Malaria Research Unit

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

Tenofovir Disoproxil Fumarate

Arm Description

Women early in pregnancy (end of first or beginning second trimester) will be treated with TDF to determine the efficacy of this strategy to bring >=95% of women to undetectable HBV DNA levels at delivery.

Outcomes

Primary Outcome Measures

The time (from inclusion through delivery; up to 6 months) to HBV DNA suppression (<100 IU/ml)
HBV DNA will be monitored every month
The proportion of women with undetectable HBV DNA at delivery
HBV DNA will be monitored at delivery.

Secondary Outcome Measures

Proportion of hepatitis B flares in mothers postpartum
All women will continue on study for 3 months after stopping TDF to measure their alanine aminotransferase (ALT) and aspartate aminotransferase (AST) monthly to detect a flare, which will be defined as >5x baseline or >10x the upper limit of normal. If at the end of the 3 months, there has been no change in ALT and AST, then the mothers will be discharged from the study. If there is an increase in liver enzymes but not a true flare, they will be followed for an additional 3 months with monthly ALT testing.
The proportion of women who adhered to TDF treatment during the course of the study (from inclusion through 1 month after delivery; up to 7 months; drug levels)
Measurement of tenofovir drug levels
The proportion of women who adhered to TDF treatment during the course of the study (from inclusion through 1 month after delivery; up to 7 months; drug accountability)
Drug accountability using standard methods (subtracting the number of tablets left from the number of tablets distributed).
The proportion of women who adhered to TDF treatment during the course of the study (from inclusion through 1 month after delivery; up to 7 months; questionnaire)
All women will be surveyed at monthly visits and at birth to measure adherence including actionable barriers.
The proportion of hepatitis B infections in the offspring at 1 year of age
Testing for HBsAg in children between 2 and 12 months of age.

Full Information

First Posted
December 8, 2016
Last Updated
February 3, 2023
Sponsor
Johns Hopkins Bloomberg School of Public Health
Collaborators
Thrasher Research Fund, Shoklo Malaria Research Unit, Chiang Mai University, University of Oxford
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1. Study Identification

Unique Protocol Identification Number
NCT02995005
Brief Title
Tenofovir in Early Pregnancy to Prevent Mother-to-child Transmission of Hepatitis B Virus
Official Title
Prevention of Mother-to-child Transmission of Hepatitis B Virus: a One Arm, Open Label Intervention Study to Estimate the Optimal Timing of Tenofovir (TDF) in Pregnancy
Study Type
Interventional

2. Study Status

Record Verification Date
October 2022
Overall Recruitment Status
Completed
Study Start Date
May 24, 2018 (Actual)
Primary Completion Date
January 31, 2023 (Actual)
Study Completion Date
January 31, 2023 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Johns Hopkins Bloomberg School of Public Health
Collaborators
Thrasher Research Fund, Shoklo Malaria Research Unit, Chiang Mai University, University of Oxford

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Product Manufactured in and Exported from the U.S.
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
Mother-to-child transmission (MTCT) of hepatitis B virus (HBV) remains the major mode of transmission in most high and intermediate HBV endemic areas, despite existing WHO immunoprophylaxis recommendations. This immunoprophylaxis regimen, if given optimally, can prevent 75-80% of HBV MTCT, but optimal implementation is difficult because it requires administering monovalent HBV vaccine and hepatitis B immunoglobulin (HBIg) within 24 hours of birth. Due to the barriers of giving HBIg, the World Health Organization (WHO) states, "…owing to concerns related to supply, safety and cost, the use of HBIg is not feasible in most settings." Clearly, global control of HBV transmission will require improved MTCT prevention. Therefore, the investigators hypothesize that treating HBV early in pregnancy will lead to undetectable HBV DNA levels at delivery and prevention of MTCT of HBV without HBIg; a concept that has already been proven with HIV. Tenofovir disoproxil fumarate (TDF), an approved anti-HBV drug, is promising to prevent MTCT of HBV due to its high potency against hepatitis B and its safety record in pregnant women. A randomized, controlled clinical trial (RCT) will be necessary to determine if TDF given to HBV-infected pregnant women early in pregnancy plus vaccine to the newborn can decrease MTCT of HBV without HBIg. However, before embarking on a RCT, several critical knowledge gaps need to be addressed including the ideal timing for TDF initiation. The purpose of this proposal is to address these knowledge gaps.
Detailed Description
The investigators hypothesize that anti-HBV therapy given in the late first or early second trimester achieves undetectable HBV DNA at delivery in >=95% of pregnant women with chronic hepatitis B. The one-arm, open-label, interventional study aims: 1, To estimate the time to complete HBV DNA suppression (<100 IU/ml) in 170 HBV DNA positive women who start TDF in the late first or early second trimester; and to estimate the proportion of women with HBV DNA <100 IU/ml at delivery. 2, To address potential barriers to and the efficacy of implementing TDF in early pregnancy to prevent mother-to-child transmission of hepatitis B. The investigators will measure potential barriers to acceptability and effectiveness of this intervention: adherence, potential hepatitis B flares in mothers (safety), and the proportion of hepatitis B infections in the offspring at 1 year of age (efficacy).

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Hepatitis B
Keywords
mother to child transmission, hepatitis B, tenofovir

7. Study Design

Primary Purpose
Prevention
Study Phase
Phase 1, Phase 2
Interventional Study Model
Single Group Assignment
Model Description
Single group study.
Masking
None (Open Label)
Masking Description
No masking, just one interventional group.
Allocation
N/A
Enrollment
98 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Tenofovir Disoproxil Fumarate
Arm Type
Experimental
Arm Description
Women early in pregnancy (end of first or beginning second trimester) will be treated with TDF to determine the efficacy of this strategy to bring >=95% of women to undetectable HBV DNA levels at delivery.
Intervention Type
Drug
Intervention Name(s)
Tenofovir Disoproxil Fumarate
Other Intervention Name(s)
Viread
Intervention Description
300 mg daily
Primary Outcome Measure Information:
Title
The time (from inclusion through delivery; up to 6 months) to HBV DNA suppression (<100 IU/ml)
Description
HBV DNA will be monitored every month
Time Frame
Up to 9 months
Title
The proportion of women with undetectable HBV DNA at delivery
Description
HBV DNA will be monitored at delivery.
Time Frame
At delivery
Secondary Outcome Measure Information:
Title
Proportion of hepatitis B flares in mothers postpartum
Description
All women will continue on study for 3 months after stopping TDF to measure their alanine aminotransferase (ALT) and aspartate aminotransferase (AST) monthly to detect a flare, which will be defined as >5x baseline or >10x the upper limit of normal. If at the end of the 3 months, there has been no change in ALT and AST, then the mothers will be discharged from the study. If there is an increase in liver enzymes but not a true flare, they will be followed for an additional 3 months with monthly ALT testing.
Time Frame
Monthly measured for 3 months after stopping TDF.
Title
The proportion of women who adhered to TDF treatment during the course of the study (from inclusion through 1 month after delivery; up to 7 months; drug levels)
Description
Measurement of tenofovir drug levels
Time Frame
Up to 9 months
Title
The proportion of women who adhered to TDF treatment during the course of the study (from inclusion through 1 month after delivery; up to 7 months; drug accountability)
Description
Drug accountability using standard methods (subtracting the number of tablets left from the number of tablets distributed).
Time Frame
Up to 9 months
Title
The proportion of women who adhered to TDF treatment during the course of the study (from inclusion through 1 month after delivery; up to 7 months; questionnaire)
Description
All women will be surveyed at monthly visits and at birth to measure adherence including actionable barriers.
Time Frame
Up to 9 months
Title
The proportion of hepatitis B infections in the offspring at 1 year of age
Description
Testing for HBsAg in children between 2 and 12 months of age.
Time Frame
Between month 2 and 12 month

10. Eligibility

Sex
Female
Minimum Age & Unit of Time
16 Years
Maximum Age & Unit of Time
49 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Pregnant women aged 18 and over HBsAg positive In the 12th-20th week of pregnancy Willing to take TDF daily during pregnancy Providing written informed consent Plans to deliver at Shoklo Malaria Research Unit (SMRU) Able and willing to comply with study requirements Exclusion Criteria: Anti-HIV positive Negative qualitative HBV DNA if HBeAg negative On immunosuppressive therapy Elevated creatinine History of kidney disease Short cervix History of pregnancy complications or prior pre-term labor
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Stephan Ehrhardt, MD
Organizational Affiliation
Johns Hopkins Bloomberg School of Public Health
Official's Role
Principal Investigator
Facility Information:
Facility Name
Shoklo Malaria Research Unit
City
Mae Sot
Country
Thailand

12. IPD Sharing Statement

Plan to Share IPD
Yes
IPD Sharing Plan Description
The investigators are currently developing an individual participant data (IPD) sharing plan.
IPD Sharing Time Frame
Data will become available 6 months after publication of the main report.
IPD Sharing Access Criteria
Permission by corresponding author
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Tenofovir in Early Pregnancy to Prevent Mother-to-child Transmission of Hepatitis B Virus

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