Hemolysis on intravenous administration of a new calcium antagonist

J Cardiovasc Pharmacol. 1995 Jun;25(6):855-8. doi: 10.1097/00005344-199506000-00001.

Abstract

Hemolysis-inducing properties of the new calcium antagonist Ro 40-5967 administered intravenously to 39 healthy male subjects were investigated in a placebo-controlled study. The volunteers were randomized into five parallel groups of 9 subjects each: three groups, receiving infusions of 40 mg Ro 40-5967 in 60, 30, and 15 min, respectively; one group receiving 80 mg Ro 40-5967 in 30 min as two simultaneous doses of 40 mg in the cubital veins of both arms; and one group receiving 80 mg Ro 40-5967 in 30 min in one arm. Within each group, 3 subjects received placebo under randomized double-blind conditions. Plasma haptoglobin decreased by 67% after 3.5 h in 2 subjects who received 80 mg Ro 40-5967 in one arm (treatment schedule thereupon discontinued). Serum bilirubin levels also increased in a dose-dependent manner in all groups as compared with placebo. Other parameters of hemolysis remained unchanged; no hemoglobinuria was observed. The intravascular hemolysis observed on infusion limits the therapeutic application of Ro 40-5967 to oral use only.

Publication types

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

MeSH terms

  • Adult
  • Benzimidazoles / administration & dosage
  • Benzimidazoles / adverse effects*
  • Benzimidazoles / therapeutic use
  • Bilirubin / blood
  • Blood Proteins / analysis
  • Blood Proteins / metabolism
  • Calcium Channel Blockers / administration & dosage
  • Calcium Channel Blockers / adverse effects*
  • Dose-Response Relationship, Drug
  • Double-Blind Method
  • Haptoglobins / metabolism
  • Hemoglobinuria / metabolism
  • Hemolysis / drug effects*
  • Humans
  • Infusions, Intravenous
  • Male
  • Mibefradil
  • Tetrahydronaphthalenes / administration & dosage
  • Tetrahydronaphthalenes / adverse effects*
  • Tetrahydronaphthalenes / therapeutic use

Substances

  • Benzimidazoles
  • Blood Proteins
  • Calcium Channel Blockers
  • Haptoglobins
  • Tetrahydronaphthalenes
  • Mibefradil
  • Bilirubin