A prospective clinical trial of D-penicillamine in the treatment of primary biliary cirrhosis

Hepatology. 1985 Nov-Dec;5(6):1139-42. doi: 10.1002/hep.1840050613.


We conducted a prospective clinical trial to assess the relative efficacy and safety of high- vs. low-dose D-penicillamine in patients with primary biliary cirrhosis. Following clinical tests and liver biopsy diagnostic of primary biliary cirrhosis, 56 patients were randomized to receive either 250 or 750 mg D-penicillamine daily. Patients were monitored with clinical tests and annual liver biopsy. Randomization produced two groups without differences in demographic, clinical or histologic characteristics. During the trial, no differences were seen between the mean change in liver test results in patients in either treatment group. The 11% per year rise of bilirubin in the 750 mg dose group during the first 3 years was not significantly different from the 18% per year rise in the 250 mg dose group. No patient showed improvement on liver biopsy although patients on 750 mg D-penicillamine deteriorated more slowly. Side effects, particularly rash and dysgeusia, were more common in the 750 mg dose group. The frequency and severity of side effects were responsible for the early conclusion of our trial. Twenty-six patients experienced side effects necessitating discontinuation of D-penicillamine. No evidence of increased efficacy was demonstrated by high-dose D-penicillamine therapy, and side effects were observed in patients on 250 mg D-penicillamine daily. With the severity of adverse effects and continued progression of disease, D-penicillamine is not a clinically useful therapy in primary biliary cirrhosis.

Publication types

  • Clinical Trial
  • Randomized Controlled Trial
  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Bilirubin / metabolism
  • Clinical Trials as Topic
  • Copper / metabolism
  • Double-Blind Method
  • Dysgeusia / chemically induced
  • Female
  • Humans
  • Liver / metabolism
  • Liver Cirrhosis, Biliary / drug therapy*
  • Liver Cirrhosis, Biliary / metabolism
  • Liver Cirrhosis, Biliary / pathology
  • Male
  • Middle Aged
  • Penicillamine / adverse effects
  • Penicillamine / therapeutic use*
  • Random Allocation
  • Skin Diseases / chemically induced


  • Copper
  • Penicillamine
  • Bilirubin