Single-dose studies of a slow-release preparation of levodopa and benserazide (Madopar HBS) in Parkinson's disease

Eur Neurol. 1987:27 Suppl 1:54-8. doi: 10.1159/000116193.

Abstract

The clinical effects and pharmacokinetic profiles of single doses of Madopar HBS were compared with those of standard Madopar in two studies in patients with Parkinson's disease and 'on-off' fluctuations. In the first study, 10 fasting patients received equivalent doses (200 mg levodopa plus 50 mg benserazide) of each preparation. The clinical response to Madopar HBS was delayed and brief; the relative bioavailability was only 50%. In the second study in 7 non-fasted patients, the effects of 3 capsules of Madopar HBS 125 were compared with those of 2 capsules of standard Madopar 125. Delay to turn on was longer with HBS, but duration of time on, and delay to turn off, were longer with this preparation. The area under the concentration-time curve for plasma levodopa was greater with HBS, and the maximum levodopa concentration was similar to, but achieved later than standard Madopar.

Publication types

  • Clinical Trial
  • Comparative Study
  • Controlled Clinical Trial

MeSH terms

  • Administration, Oral
  • Adult
  • Aged
  • Benserazide / administration & dosage
  • Benserazide / pharmacokinetics
  • Benserazide / therapeutic use*
  • Biological Availability
  • Clinical Trials as Topic
  • Delayed-Action Preparations
  • Drug Combinations / pharmacokinetics
  • Drug Combinations / therapeutic use
  • Humans
  • Hydrazines / therapeutic use*
  • Levodopa / administration & dosage
  • Levodopa / pharmacokinetics
  • Levodopa / therapeutic use*
  • Middle Aged
  • Parkinson Disease / drug therapy*
  • Random Allocation

Substances

  • Delayed-Action Preparations
  • Drug Combinations
  • Hydrazines
  • benserazide, levodopa drug combination
  • Levodopa
  • Benserazide