Maternal Therapy With TAF Versus TDF to Prevent Vertical Transmission of Hepatitis B

Pregnancy Related Clinical Trial

Official title:

Real World Study of Tenofovir Alafenamide Versus Tenofovir Disoproxil Fumarate to Prevent Vertical Transmission of Hepatitis B in Mothers With High Viral Load

Clinical Trial Details — Status: Recruiting

Administrative data

• NCT number: NCT04211805
• Other study ID #: CN-P919-2020
• Status: Recruiting
• Start date: January 27, 2020
• Est. completion date: September 30, 2021

Study information

• Verified date: December 2020
• Source: New Discovery LLC
• Contact: Harry Huang, BS
• Phone: (+1)5163048196
• Email: harry.huang887[@]gmail.com
• Is FDA regulated: No
• Study type: Observational

Clinical Trial Summary

Immunoprophylaxis failure of hepatitis B (HBV) remains a concern and has been reported in approximately 10-30% of infants born to highly viremic mothers with HBeAg-positive. Maternal HBV DNA >6log10 copies/mL (or 200,000 IU/mL) is the major independent risk for mother-to-child transmission (MTCT). 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 when compared 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) with few adverse effects. TAF however, has a better safety profile with less adverse effects to bone mineral density and renal function. The present prospective, double-arm study is to evaluate the non-inferiority in the efficacy and safety of TAF therapy versus TDF therapy in highly viremic mothers and their infants for the prevention of MTCT in the real world setting.

Description:

This is a prospective, double-arm, multi-center study conducted through 11 centers across China. Consecutive 450 mothers who are eligible for the study will be enrolled during gestational weeks 24-28 to receive TDF or TAF based on the patients' preference, and the treatment will be discontinued right after the delivery. All infants will receive HBV vaccination plus HBIg within 12 hours after birth and the additional HBV vaccination at the age of 4 weeks and 24 weeks. Primary outcome assessment will be performed at the infants' age of 28 will be collected to evaluate non-inferiority in the safety and efficacy of TAF therapy versus TDF therapy. These parameters will be extracted from test results of serum biochemistries, hematology, and virology, including but not limited to aspartate aminotransferase (AST), ALT, HBV DNA levels, and serological status of HBV (HBsAg, HBeAb, HBcAb, HBeAg, and HBsAg). All aforementioned clinical parameters will be extracted from mothers at the following timepoints for assessment: the baseline, i.e. the start of TAF/TDF treatment, gestational weeks 28, 32, 36, on delivery, and at postpartum weeks 24-28. For the infant, information from two timepoints, at birth and at infant age of 28 weeks, will be collected. This information regarding the infant will include the physical parameters weight, height, head circumference, HBV DNA levels, HBV serological status, if they received hepatitis B immunoglobin (HBIg), if they received the complete series of HBV vaccine. All relevant information regarding the patient will be logged into a password-protected computer for primary and secondary analysis. Group A: 225 participating mothers will receive TAF (oral 25 mg tablet daily) starting at gestational week 24-28 of pregnancy and continue until delivery. The mothers will be followed together with their infants until postpartum week 28.Infants will receive hepatitis B vaccine plus HBIg at birth (within 12 hours) and additional hepatitis B vaccine at the age of week 4 and week 24. Group B: 225 participating mothers will receive TDF (oral 300 mg tablet daily) starting at gestational week 24-28 of pregnancy and continue until delivery. Patients in group B will have similar follow-up schedules as those in the Group A. Infants will receive hepatitis B vaccine plus HBIg at birth (within 12 hours) and additional hepatitis B vaccine at the age of week 4 and week 24.

Recruitment information / eligibility

• Status: Recruiting
• Enrollment: 450
• Est. completion date: September 30, 2021
• Est. primary completion date: September 30, 2021
• Accepts healthy volunteers: No
• Gender: Female
• Age group: 18 Years and older

Eligibility

Inclusion Criteria:

1. Pregnant female, above 18 years of age and under 40 years of age.

2. Gestational age between 12-14 weeks (The screening on patients can be started at gestational week 12).

3. Documented compensated and stable chronic hepatitis B defined by all of the following:

• HBsAg persistently positive > 6 months.
• Clinical history, physical findings, and test results are compatible with compensated chronic hepatitis B.

4. Detectable maternal serum HBsAg and HBeAg at the screening visit.

5. Maternal serum HBV DNA levels exceeding 200,000 IU/mL by the COBAS Amplicor HBV PCR assay at screening visits.

6. Patient is willing and able to comply with the study drug regimen and all other study requirements. Patient is also willing to prevent another pregnancy in 28 weeks after delivery of the current baby.

7. Patient and her husband (both father and mother of the child) understand the risk and are willing to have the mother participating in the study. The mother must be willing and able to provide written informed consent to participate in the study. Exclusion Criteria:

Patients will be excluded if they have any one of the following:

1. Creatinine clearance <100 mL/min (using the Cockcroft-Gault method based on serum creatinine and ideal body weight) or hypo-phosphoremia (below normal range).

2. History of renal events on adefovir or history of resistance to adefovir.

3. Hemoglobin <8 g/dL, or neutrophil count <1000/uL, or ALT >5 times ULN, or total bilirubin >2 mg/dL; or albumin <25gm/L, or abnormal creatinine level, or abnormal BUN levels.

4. History of abortion, or congenital malformation, or child infected with HBV in a prior pregnancy.

5. Biological father of the child (current pregnancy) has CHB.

6. Significant renal, cardiovascular, pulmonary, or neurological disease that may impact the subject's participation in the study as per the opinion of the investigator.

Related Conditions & MeSH terms

• Hepatitis
• Hepatitis A
• Hepatitis B
• Hepatitis B, Chronic
• Pregnancy Related

Intervention

Drug:
• Tenofovir Alafenamide 25 MG for arm (A)
Tenofovir Alafenamide (TAF) will be provided, 25 mg Per Oral daily.
• Tenofovir Disoproxil Fumarate 300mg for arm (B)
Tenofovir Disoproxil Fumarate (TDF) will be provided, 300 mg Per Oral daily.

Locations

Country	Name	City	State
China	Xiangya Hospital, Central South University	Changsha	Hunan
China	First Affiliated Hospital of Fujian Medical University	Fuzhou	Fujian
China	Ganzhou Fifth People's Hospital	Ganzhou	Jiangxi
China	Hainan General Hospital	Haikou	Hainan
China	The Fourth Hospital of Harbin Medical University	Harbin	Heilonjiang
China	Shanghai Public Health Clinical Center, Fudan University	Jinshan	Shanghai
China	The Third Hospital of Qinhuangdao	Qinhuangdao	Hebei
China	Pingdingshan Hospital of Chongqing Public Health Medical Treatment Center	Shapingba	Chongqing
China	Shengjing Hospital of China Medical University	Shenyang	Liaoning
China	The Seventh Affiliated Hospital, Sun Yat-sen University	Shenzhen	Guangdong
China	Yuyao People's Hospital of Zhejiang Province	Yuyao	Zhejiang

Sponsors (1)

Lead Sponsor	Collaborator
New Discovery LLC

Country where clinical trial is conducted

China, 

References & Publications (5)

Jourdain G, Ngo-Giang-Huong N, Harrison L, Decker L, Khamduang W, Tierney C, Salvadori N, Cressey TR, Sirirungsi W, Achalapong J, Yuthavisuthi P, Kanjanavikai P, Na Ayudhaya OP, Siriwachirachai T, Prommas S, Sabsanong P, Limtrakul A, Varadisai S, Putiyanun C, Suriyachai P, Liampongsabuddhi P, Sangsawang S, Matanasarawut W, Buranabanjasatean S, Puernngooluerm P, Bowonwatanuwong C, Puthanakit T, Klinbuayaem V, Thongsawat S, Thanprasertsuk S, Siberry GK, Watts DH, Chakhtoura N, Murphy TV, Nelson NP, Chung RT, Pol S, Chotivanich N. Tenofovir versus Placebo to Prevent Perinatal Transmission of Hepatitis B. N Engl J Med. 2018 Mar 8;378(10):911-923. doi: 10.1056/NEJMoa1708131. — View Citation

Pan CQ, Duan Z, Dai E, Zhang S, Han G, Wang Y, Zhang H, Zou H, Zhu B, Zhao W, Jiang H; China Study Group for the Mother-to-Child Transmission of Hepatitis B. Tenofovir to Prevent Hepatitis B Transmission in Mothers with High Viral Load. N Engl J Med. 2016 Jun 16;374(24):2324-34. doi: 10.1056/NEJMoa1508660. — View Citation

Wiseman E, Fraser MA, Holden S, Glass A, Kidson BL, Heron LG, Maley MW, Ayres A, Locarnini SA, Levy MT. Perinatal transmission of hepatitis B virus: an Australian experience. Med J Aust. 2009 May 4;190(9):489-92. — View Citation

Xu WM, Cui YT, Wang L, Yang H, Liang ZQ, Li XM, Zhang SL, Qiao FY, Campbell F, Chang CN, Gardner S, Atkins M. Lamivudine in late pregnancy to prevent perinatal transmission of hepatitis B virus infection: a multicentre, randomized, double-blind, placebo-controlled study. J Viral Hepat. 2009 Feb;16(2):94-103. doi: 10.1111/j.1365-2893.2008.01056.x. Epub 2008 Oct 8. — View Citation

Zou H, Chen Y, Duan Z, Zhang H. Protective effect of hepatitis B vaccine combined with two-dose hepatitis B immunoglobulin on infants born to HBsAg-positive mothers. PLoS One. 2011;6(10):e26748. doi: 10.1371/journal.pone.0026748. Epub 2011 Oct 28. — View Citation

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Assessment on the Proportion of Infants who are Infected with Hepatitis B at the Age of 28 Weeks in the Two Groups	Compare MTCT rates between the two study groups and demonstrate non-inferiority in efficacy. MTCT rate is defined as the proportion of infants with serum HBV DNA >20 IU/mL and/or HBsAg positivity at 28 weeks of age.	From the date of birth to the age of 24-28 weeks
Primary	Assessment on Congenital Defects and/or Malformation Rates in Each Infant Group for Comparison	The rate of congenital defects and/or malformation rates in infants. Congenital defects and/or malformation rates are defined as the proportion of infants with the aforementioned abnormalities discovered during the study period. The rate of infant congenital defect/malformation as determined in group A will be compared with that of group B.	from the date of birth to Infant's age of 24-28 weeks
Secondary	Assessment on the change in Maternal HBV DNA Levels at Delivery	Assess the change in maternal HBV DNA levels (IU/mL) at delivery when compared to the baseline before initiating TAF/TDF.	from gestational week 24-28 week to delivery
Secondary	Maternal Serological Outcomes During the Study: Percentage of Mothers who Loss/Seroconversion of HBsAg or/and HBeAg During the Study	Assess the percentage of mothers who loss/seroconversion of HBsAg or/and HBeAg during the study. Loss is defined by a test showing a negative HBsAg/HBeAg result at the end of the trial, given a positive respective test result at baseline. A seroconversion is defined as a test showing a negative HBsAg and a positive HBsAb result, or a negative HBeAg and a positive HBeAb result at the end of the trial, given a positive HBsAg/HBeAg test result at baseline. The proportion of mothers who experience loss/seroconversion as determined in group A will be compared with that of group B.	from gestational week 24-28 week to postpartum week 28
Secondary	Incidence of Treatment-Emergent Adverse Events in Mothers as Stratified by the CTCAE v 5.0	Assess the percentage of Mothers who have adverse events during the study, graded by the Common Terminology Criteria for Adverse Events (CTCAE), version 5.0. The proportion of mothers who experience adverse events as determined in group A will be compared with that of group B.	Gestational week 24-28 until Postpartum Week 28
Secondary	Incidence of Treatment-Emergent Adverse Events in Infants as Stratified by the CTCAE v 5.0	Assess the percentage of infants who have adverse events during the study, graded by the Common Terminology Criteria for Adverse Events (CTCAE), version 5.0. The proportion of infants who experience adverse events as determined in group A will be compared with that of group B.	Delivery until Infant age Week 28
Secondary	Percentage of Mothers with Alanine transferase (ALT) Levels Within the Normal Limit	To calculate the percentage of mothers at postpartum 28 weeks whose ALT (U/L) levels stay within the normal limit in response to therapy. The proportion of mothers whose ALT levels who stay within the normal limit as determined in group A will be compared with that of group B.	Gestational week 24-28 until Postpartum week 28
Secondary	Percentage of Mothers with Aspartamine transferase (AST) Levels Within the Normal Limit	To calculate the percentage of mothers at postpartum 28 weeks whose AST (U/L) levels stay within the normal limit in response to therapy. The proportion of mothers whose AST levels who stay within the normal limit as determined in group A will be compared with that of group B.	Gestational week 24-28 until Postpartum week 28
Secondary	Group A: Proportion of Infants Born to Mothers Who Received TAF, Whose Physical Growth Characteristics Stay Within the Published National Normal Range.	Physical growth characteristics of the infants, born to mothers who received TAF, at the time points on birth and infant age of 24-28 weeks will be compared with the normal range of the national database published in recent years and analyzed. The proportion of infants whose growth characteristics are outside the published national range at the end of the study as determined in group A will be compared with that of group B.	Delivery to Infant age 28 weeks
Secondary	Group B: Proportion of Infants Born to Mothers Who Received TDF, Whose Physical Growth Characteristics Stay Within the Published National Normal Range.	Physical growth characteristics of the infants, born to mothers who received TDF, at the time points on birth and infant age of 24-28 weeks will be compared with the normal range of the national database published in recent years and analyzed.The proportion of infants whose growth characteristics are outside the published national range at the end of the study as determined in group A will be compared with that of group B.	Delivery to Infant age 28 weeks
Secondary	Tolerability of TDF vs TAF Therapy: Percentage of Mothers who Discontinue Therapy Due to the Adverse Event(s) During the Study.	Assess the percentage of mothers who discontinue therapy due to the adverse event(s) during the study. The proportion of mothers who discontinue therapy as determined in group A will be compared with that of group B.	Gestational week 24-28 until Delivery