The Efficacy and Safety of Nucleos(t)Ide Analogues in the Treatment of HBV-related Acute-on-chronic Liver Failure

Hepatitis B Clinical Trial

Official title:

A Multicenter Controlled Open-label Trial of Evaluating Tenofovir Alafenamide, Tenofovir Disoproxil Fumarate and Entecavir in Acute-on-chronic Liver Failure of Chronic Hepatitis B Patients

Clinical Trial Details — Status: Recruiting

Administrative data

• NCT number: NCT03640728
• Other study ID #: XJTU1AF2018LSL-002
• Status: Recruiting
• Start date: January 25, 2019
• Est. completion date: July 2023

Study information

• Verified date: February 2023
• Source: First Affiliated Hospital Xi'an Jiaotong University
• Contact: Juan Li, M.D.
• Phone: 18209272726
• Email: lijuan1996xx[@]163.com
• Is FDA regulated: No
• Study type: Observational

Clinical Trial Summary

HBV-related acute-on-chronic liver failure (ACLF) is a clinical syndrome defined as acute hepatic insult with diagnosed or undiagnosed chronic liver disease. Current clinical guidelines advocate oral antiviral treatment in HBV-related ACLF. However, no conclusion on which nucleoside analogue is the most satisfactory drug for the treatment of HBV-related liver failure has not been reached yet. In this cohort study, the investigators will compare the efficacy, safety, and tolerability of tenofovir alafenamide (TAF), Tenofovir Disoproxil Fumarate (TDF) and entecavir (ETV) in HBV-related ACLF in China. In addition, the drug metabolism characteristics of TAF will be explored in such severe liver injury population of HBV-ACLF.

Description:

Potent antivirals like entecavir (ETV), Tenofovir Disoproxil Fumarate (TDF) and Tenofovir alafenamide (TAF) now are recommended as first-line therapy for patients with chronic HBV infection because of their significant suppression of viral replication and a high barrier to resistance. HBV-related acute-on-chronic liver failure (ACLF) is a clinical syndrome defined as acute hepatic insult with diagnosed or undiagnosed chronic liver disease. Only a limited number of medical treatments are available for ACLF. Although liver transplantation is a life-saving treatment for ACLF, the difficulty in finding a suitable donor and the high cost hinder its extensive clinical use.

The precise mechanism underlying the liver injury caused by HBV-related ACLF and the factors contributing to the progression of liver failure remain unknown. HBV DNA replication is one of the key factors causing the progression from liver damage to liver failure. Current clinical guidelines advocate oral antiviral treatment in HBV-related ACLF. However, the specific antiviral treatment for patients with liver failure remains unclear. In the past years, efficacy of nucleoside analogues, such as lamivudine, entecavir, telbivudine and tenofovir, for HBV-related liver failure has been reported. However, no conclusion on which nucleoside analogue is the most satisfactory drug for the treatment of HBV-related liver failure has not been reached yet.

In this cohort study, the investigators will compare the efficacy, safety, and tolerability of tenofovir alafenamide (TAF), Tenofovir Disoproxil Fumarate (TDF) and entecavir (ETV) in HBV-related ACLF in China. In addition, pharmacokinetic properties of TAF tablets will be explored in the study subjects.

Recruitment information / eligibility

• Status: Recruiting
• Enrollment: 200
• Est. completion date: July 2023
• Est. primary completion date: April 30, 2021
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years to 70 Years

Eligibility

Inclusion Criteria:All of below

1. age 18-70 years, male or female.

2. HBsAg positive at least 6 months or more, HBeAg positive or negative.

3. Serum HBV DNA positive (Serum HBV DNA should be determined by the PCR assay at the local laboratory at screening for this study)

4. Recent development of increasing jaundice (a total serum bilirubin concentration of above 85µmol/L) and coagulopathy (INR =1.5 or prothrombin activity<40%)

5. Recent development of complications such as hepatic encephalopathy, or abrupt and obvious increase in ascites, or spontaneous bacterial peritonitis, or hepatorenal syndrome.

6. Patient is willing and able to comply with the study drug regimen and all other study requirements.

7. The patient is willing and able to provide written informed consent to participate in the study.

Exclusion Criteria: Any of below

1. Patient has concomitant other chronic viral infection (HCV or HIV)

2. Patient has evidence of renal insufficiency defined as serum creatinine > 1.5 mg/dL

3. Patient has medical condition that requires concurrent use of systemic prednisolone or other immunosuppressive agent (including chemotherapeutic agent)

4. Patient is pregnant or breastfeeding or willing to be pregnant

5. Patient has one or more additional known primary or secondary causes of liver disease, other than hepatitis B (e.g., alcoholism, autoimmune hepatitis, malignancy with hepatic involvement, hemochromatosis, alpha-1 antitrypsin deficiency, Wilson's Disease, other congenital or metabolic conditions affecting the liver, congestive heart failure or other severe cardiopulmonary disease, etc.).

6. A history of treated malignancy (other than hepatocellular carcinoma) is allowable if the patient's malignancy has been in complete remission, off chemotherapy and without additional surgical intervention, during the preceding three years.

7. Active ethanol/drug abuse/psychiatric problems such as major depression, schizophrenia, bipolar illness, obsessive-compulsive disorder, severe anxiety, personality disorder that might interfere with participation in the study.

8. Current alcohol or substance abuse judged by the investigator to potentially interfere with participant compliance.

Related Conditions & MeSH terms

• Acute-On-Chronic Liver Failure
• End Stage Liver Disease
• Hepatic Insufficiency
• Hepatitis
• Hepatitis A
• Hepatitis B
• Liver Failure
• Virus Diseases

Intervention

Drug:
• Tenofovir Alafenamide
Tenofovir alafenamide 25 mg/day orally
• Entecavir
Entecavir 0.5 mg/day orally
• Tenofovir disoproxil fumarate
Tenofovir Disoproxil Fumarate 300 mg/day orally

Locations

Country	Name	City	State
China	Ankang Central Hospital	Ankang
China	Hanzhong 3201 Hospital	Hanzhong
China	Hanzhong Infectious Hospital	Hanzhong
China	Weinan Central Hospital	Weinan
China	First Affiliated Hospital Xi'an Jiaotong University	Xi'an
China	Shaanxi provincial people's hospital	Xi'an
China	Tangdu Hospital, The Fourth Military Medical University,	Xi'an
China	The Second Affiliated Hospital of Xi'an Jiaotong University	Xi'an
China	Xi'an Central Hospital	Xi'an
China	Xijing Hospital, The Fourth Military Medical University	Xi'an
China	The Affiliated Hospital of Yan'an University	Yan'an

Sponsors (1)

Lead Sponsor	Collaborator
First Affiliated Hospital Xi'an Jiaotong University

Country where clinical trial is conducted

China, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Overall survival of ACLF subjects	Overall survival in subjects with acute-on-chronic liver failure will be summarized and compared with control subjects through study day 28 and week 48.	study day 1 through week 48
Secondary	Changes in serum HBV DNA levels		at week 4 and 48 of treatment
Secondary	Proportion of patients with hepatitis B e-Ag(HBe-Ag) loss or seroconversion		at week 4 and 48 of treatment
Secondary	Proportion of patients with HBs-Ag loss or seroconversion		at week 4 and 48 of treatment
Secondary	Proportion of patients with normal alanine aminotransferase(ALT)		at week 4 and 48 of treatment
Secondary	Liver function evaluation through Model for End-Stage Liver Disease (MELD) scores	Model for End-Stage Liver Disease(MELD) Score is calculated according to the equation:3.78×ln[serum bilirubin (mg/dl)] + 11.2×ln(INR) + 9.57×ln[serum creatinine (mg/dL)] + 6.43. Liver function improvement defined as the decline of total MELD score, whereas liver function deterioration defined as the rise of total MELD score. The risk of death increased when total MELD score above 25.	at week 4 and 48 of treatment
Secondary	Proportion of patients with virologic breakthrough	Virologic breakthrough is defined as the increase in serum HBV DNA by >1 log10 (10-fold) above nadir after achieving virologic response as determined by at least 2 consecutive measurements of at least 2 weeks apart, during continued treatment	at week 4 and 48 of treatment
Secondary	Proportion of patients with complete virologic response	Virologic response is defined as the serum HBV DNA concentrations below 20 IU/mL	at week 4 and 48 of treatment