Plasma concentrations and effect on testosterone metabolism after single doses of MK-0434, a steroid 5 alpha-reductase inhibitor, in healthy subjects

Eur J Clin Pharmacol. 1994;46(2):123-6. doi: 10.1007/BF00199874.

Abstract

A four-period, two-panel, single-rising-dose study (0.1-100 mg) was conducted in healthy males to investigate the pharmacodynamics, tolerability and pharmacokinetics of MK-0434, a steroid 5 alpha-reductase inhibitor. MK-0434 was associated with a significant reduction in dihydrotestosterone, which was maximal at 24 h and maintained through 48 h post treatment. The maximum reduction was approximately 50% and occurred at all doses above 5 mg (10, 25, 50 and 100 mg). MK-0434 appeared to have no effect on serum testosterone at these single doses. Rising single doses of MK-0434 were associated with an increase in Cmax and AUC but the changes were less than proportional to dose, most likely due to nonlinear absorption. MK-0434 given in single doses up to 100 mg was without significant adverse effects in healthy male volunteers. In summary, MK-0434 is a well-tolerated, potent, orally active 5 alpha-reductase inhibitor in man.

MeSH terms

  • 5-alpha Reductase Inhibitors*
  • Adult
  • Dihydrotestosterone / blood*
  • Finasteride / administration & dosage
  • Finasteride / analogs & derivatives*
  • Finasteride / blood
  • Finasteride / pharmacology
  • Humans
  • Male
  • Reference Values

Substances

  • 17 beta-benzoyl-4-aza-5 alpha-androst-1-ene-3-one
  • 5-alpha Reductase Inhibitors
  • Dihydrotestosterone
  • Finasteride