SUMMARY A randomised controlled trial was conducted in 29 HBV carriers who had been HBs and HBe antigen positive for more than six months. Fifteen patients were treated with ARA-AMP 10 mg/kg/day given as intramuscular injections 12 hours apart for five days followed by 5 mg/kg/day for 23 days. The 14 controls received no treatment. Serum HBV-DNA polymerase, and HBV-DNA decreased in all patients during therapy. Six treated patients lost serum HBV-DNA polymerase, HBV-DNA and HBeAg, HBsAg concentrations decreased, and five developed anti-HBe. One of these six patients lost HBsAg and developed anti-HBs. No such changes were observed in the control group over a similar 18 month period of observation. A four week course of ARA-AMP inhibits HBV replication and in a significant minority of patients this is long lasting and is associated with a reduced level of inflammatory activity in the liver.Adenine arabinoside (ARA-A) is a synthetic purine nucleoside with anti-viral activity against a large number of DNA viruses.1 It has been used, largely in uncontrolled studies, in patients with chronic liver disease caused by hepatitis B virus (HBV) infection. In the majority of those treated, a transient decrease in HBV-DNA polymerase (HBV-DNAp) has been observed with no change in HBsAg concentration, HBeAg status, liver function tests or histology. In a minority of patients, however, inhibition of HBVDNAp is prolonged beyond the treatment period with a decrease in HBsAg concentration, loss of HBeAg and the development of anti-HBe.2 -Similarly, in uncontrolled studies with ARA-A and/or human leucocyte interferon, 37% of treated patients have shown this prolonged inhibition of HBV replication with HBeAg to anti-HBe seroconversion, accompanied by an improvement in liver function tests and histology.6 7 Spontaneous HBeAg to anti-HBe seroconversion does occur, however, with a variable frequency in different populations and may occur following withdrawal of immuno-