[Effective long-term treatment of primary hyperlipoproteinemias with bezafibrate]

Schweiz Med Wochenschr. 1985 Jun 29;115(26):907-11.
[Article in German]

Abstract

Bezafibrate, a new hypolipidemic agent, was evaluated in a single blind, placebo-controlled study lasting 14 months to 3 years in 40 patients with primary hyperlipoproteinemia of various types (23 patients with type II, 15 with type IV and 2 with type V). Bezafibrate in a dose of 200 mg 3 times daily reduced total serum cholesterol by an average of 17% (p less than 0.001) in hyperlipoproteinemia type II and by 24% (p less than 0.001) in type IV or V, lowered serum triglycerides by 31% (p less than 0.001) in hyperlipoproteinemia type II and by 58% (p less than 0.001) in type IV or V, while high-density-lipoprotein-cholesterol was increased by 17% (p less than 0.001) in type II and by 36% (p less than 0.001) in type IV or V. The few side effects encountered were only mild and transient. These findings show that bezafibrate affords safe and effective long-term treatment of patients with hyperlipoproteinemia.

Publication types

  • Clinical Trial
  • Controlled Clinical Trial
  • English Abstract
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Aged
  • Alkaline Phosphatase / metabolism
  • Bezafibrate / therapeutic use*
  • Cholesterol / blood
  • Cholesterol, HDL / blood
  • Clinical Trials as Topic
  • Creatine Kinase / metabolism
  • Creatinine / blood
  • Female
  • Humans
  • Hyperlipoproteinemia Type II / drug therapy
  • Hyperlipoproteinemia Type IV / drug therapy
  • Hyperlipoproteinemia Type V / drug therapy
  • Hyperlipoproteinemias / blood
  • Hyperlipoproteinemias / drug therapy*
  • Long-Term Care
  • Male
  • Middle Aged
  • Placebos
  • Triglycerides / blood

Substances

  • Cholesterol, HDL
  • Placebos
  • Triglycerides
  • Cholesterol
  • Creatinine
  • Creatine Kinase
  • Alkaline Phosphatase
  • Bezafibrate