Halting Nucleoside Analogues in Chronic Hepatitis B (HALT-NUCS)

Seng Gee Lim

Status: Active, not recruiting

Conditions: Chronic Hepatitis B

Treatments: Other: stopping nucleos(t)ide therapy; Other: Continue nucleos(t)ide analogue

Study type: Interventional

Funder types: Other

Identifiers

NCT04102176

CIRG17may042

Details and patient eligibility

About

Most patients with Chronic Hepatitis B are on nucleoside analogy (NA) long term, but this leads to HBsAg loss (defined as functional cure) of only 2% at 6 years. Recently a number of studies have shown significant HBsAg loss rates after stopping nucleoside analogues (NA). However, no criteria to select such patients have been evaluated. Consequently, the objective of the study is not only to determine the proportion of patients able to achieve HBsAg loss in those with qHBsAg≤100IU/ml. The study is designed as a randomised control trial with 1:2 parallel arm randomisation to continuing NA or stopping therapy. Patients will be monitored after stopping therapy for Hepatitis B flares and also to document HBsAg loss.

Full description

Chronic Hepatitis B (CHB) affects over 250 million persons and is considered one of the major causes of mortality and morbidity globally. Standard treatment consists of nucleos(t)ide analogues (NA) or peginterferon (PEG). There has been increasing interested in HBsAg loss, defined as functional cure. However this has been difficult to achieve with NA, and although rates of HBsAg loss are higher with PEG, they are still <10%. However, a number of studies have shown that HBsAg loss rates were significantly higher in those who stopped NA. A study from Greece by Hadziyannis had a 39% HBsAg loss after patients stopped adefovir therapy. Further studies have shown similar results, and those not able to clear HBsAg have had quiescent disease, although some patients had to restart therapy usually due to hepatitis B flares. No deaths have been reported. Consequently, while stopping therapy has led to HBsAg loss in some patients, it is not clear which patients would benefit the most. The prior studies have indicated that patients most likely to lose HBsAg had low qHBsAg levels and a level ≤100 IU/ml had a high possibility of HBsAg loss. Consequently, we propose to test whether patients with CHB on NA >1year and without liver cirrhosis and with qHBsAg≤100 IU/ml are able to lose HBsAg compared to those who continue NA. The study is designed as a parallel arm RCT randomised 1:2 to continue NA versus stop NA. Patients will be monitored regularly for clinical status, virological markers, and liver markers. The primary endpoint is HBsAg loss at the end of the study in those who stop versus those who continue NA. Additional outcomes will be hepatitis B flares, inactive hepatitis B status, virological relapse, and restarting therapy.

Enrollment: 120 patients

Sex: All

Ages: 21 to 70 years old

Volunteers: No Healthy Volunteers

Inclusion criteria

• • Between 21 and 75 years old.

  • Documented to be HBsAg positive for ≥ 6 months.
  • On any NA (lamivudine, adefovir, entecavir, telbivudine tenofovir) for ≥ 1 year
  • HBV DNA <15 IU/ml at screening (undetectable)
  • Quantitative HBsAg <100 IU/ml
  • Patient has agreed not to take any other investigational drug or systemic anti-viral, cytotoxic, corticosteroid, immunomodulatory agents or Chinese traditional remedies unless clinically indicated.
  • Patient is able to give written consent prior to study start and to comply with the study requirements.
  • Women of childbearing age must have a negative serum (ß-HCG) pregnancy test taken with 14 days of starting therapy

Exclusion criteria

• • Evidence of liver cirrhosis based on liver biopsy, fibroscan score >10.5 kpa, or MRE score>5.5kpa, or clinical evidence of cirrhosis demonstrated by presence of esophageal varices, obvious features of cirrhosis on ultrasound within the last 12 months

  • Evidence of decompensated liver disease or hepatocellular carcinoma.
  • HIV antibody or HCV antibody or HDV antibody positivity
  • Creatinine > 1.5 times upper limit of normal
  • INR > 1.5, uncorrected by Vitamin K therapy.
  • Any interferon, Immunomodulators, systemic cytotoxic agents, or systemic corticosteroids within 6 months before trial entry.
  • Prolonged exposure to known hepatotoxins such as alcohol or drugs.
  • History of clinically relevant psychiatric disease, seizures, central nervous system dysfunction, severe pre-existing cardiac, renal, hematological disease or medical illness that in the investigator's opinion might interfere with therapy.
  • Malignant disease within 5 years of trial entry.
  • Women who are pregnant and who are not practicing adequate birth control measures, or who are lactating

Trial design

Primary purpose: Treatment

Allocation: Randomized

Interventional model: Parallel Assignment

Masking: None (Open label)

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120 participants in 2 patient groups

Continue nucleos(t)ide analogue

Active Comparator group

Description:

patients will be given open label tenofovir alafenamide

Treatment:

Other: Continue nucleos(t)ide analogue

Stopping nucleos(t)ide analogue

Experimental group

Description:

patients will stop nucleos(t)ide therapy (such as entecavir, tenofovir, lamivudine or adefovir)

Treatment:

Other: stopping nucleos(t)ide therapy