Novel statins: pharmacological and clinical results

Cardiovasc Drugs Ther. 2002 May;16(3):251-7. doi: 10.1023/a:1020656607497.

Abstract

Rosuvastatin (ZD4522) and pitavastatin (NK-104) are novel HMG-CoA reductase inhibitors with a peculiar pharmacological profile. In particular, they show a high potency in decreasing LDL-C and their catabolism is not mediated by the cytochrome P-450 3A4, thus reducing the potential for drug-drug interaction and improving the management of blood cholesterol. As the magnitude of LDL-C reduction is directly associated with the decrease in the incidence of myocardial infarction and mortality for CAD, statins with increased LDL-C lowering potency may ensure the achievement of target LDL-C levels and offer a more aggressive cholesterol control, further improving CAD morbidity and mortality.

Publication types

  • Review

MeSH terms

  • Animals
  • Cholesterol, LDL / blood
  • Clinical Trials as Topic
  • Coronary Disease / blood
  • Coronary Disease / etiology
  • Coronary Disease / prevention & control
  • Fluorobenzenes / pharmacokinetics
  • Fluorobenzenes / pharmacology
  • Fluorobenzenes / therapeutic use
  • Humans
  • Hydroxymethylglutaryl-CoA Reductase Inhibitors / pharmacology*
  • Hypercholesterolemia / complications
  • Hypercholesterolemia / drug therapy
  • Naphthalenes / pharmacokinetics
  • Naphthalenes / pharmacology
  • Naphthalenes / therapeutic use
  • Pyrimidines*
  • Quinolines / pharmacokinetics
  • Quinolines / pharmacology
  • Quinolines / therapeutic use
  • Rosuvastatin Calcium
  • Sulfonamides*

Substances

  • Cholesterol, LDL
  • Fluorobenzenes
  • Hydroxymethylglutaryl-CoA Reductase Inhibitors
  • LFA703
  • Naphthalenes
  • Pyrimidines
  • Quinolines
  • Sulfonamides
  • Rosuvastatin Calcium
  • pitavastatin