Literature DB >> 9740538

Extending therapy options in treating lipid disorders: a clinical review of cerivastatin, a novel HMG-CoA reductase inhibitor.

E A Stein1.   

Abstract

Cerivastatin is a third generation pure enantiomeric HMG-CoA reductase inhibitor. It reduces low density lipoprotein (LDL)-cholesterol by 22 to 44% at doses of 0.1 to 0.8 mg/day. The drug has been extensively evaluated for more than 5 years in clinical trials and is currently marketed in a number of countries at doses of 0.1 to 0.3 mg/day. Cerivastatin has been tested in more than 4000 patients during extensive phase II and III studies. About 40% of patients in these trials were women, and many participants were aged between 65 and 75 years. The trial populations had moderate to severe hypercholesterolaemia, with mean baseline LDL-cholesterol levels of approximately 5.2 mmol/L (200 mg/dl). In large phase III trials, cerivastatin, over the dosage range of 0.1 to 0.4 mg/day, reduced LDL-cholesterol by 22.4 to 36.1% from baseline. As with other HMG-CoA reductase inhibitors, the log-linear dose-response curve of cerivastatin showed a 6% additional decrease in mean LDL-cholesterol levels for each doubling of the daily dose, with no plateau effect noted at the highest dosage yet tested (0.8 mg/day). High density lipoprotein cholesterol levels increased by 4 to 10% during cerivastatin therapy. This effect, which was consistent with that of other HMG-CoA reductase inhibitors, was not dose related. As has been found with other statins, the triglyceride-lowering effects of cerivastatin are dependent on baseline triglyceride levels, with very small reductions occurring in patients with low initial levels [< 1.7 mmol/L (150 mg/dl)], and larger dose-dependent reductions of up to 36% with the 0.4 mg/day dose observed in patients with baseline triglyceride levels >2.8 mmol/L (250 mg/dl). Cerivastatin was well tolerated in all studies. Cerivastatin recipients and recipients of other HMG-CoA reductase inhibitors experienced a similar incidence of adverse events (including hepatic transaminase elevations) in comparative studies. Cerivastatin is an effective and safe lipid-lowering agent for most patients with hypercholesterolaemia.

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Year:  1998        PMID: 9740538     DOI: 10.2165/00003495-199856001-00004

Source DB:  PubMed          Journal:  Drugs        ISSN: 0012-6667            Impact factor:   9.546


  13 in total

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2.  The rule of 5 and the rule of 7 in lipid-lowering by statin drugs.

Authors:  W C Roberts
Journal:  Am J Cardiol       Date:  1997-07-01       Impact factor: 2.778

3.  Cerivastatin, a New Potent Synthetic HMG Co-A Reductase Inhibitor: Effect of 0.2 mg Daily in Subjects With Primary Hypercholesterolemia.

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Journal:  J Cardiovasc Pharmacol Ther       Date:  1997-01       Impact factor: 2.457

4.  The efficacy and six-week tolerability of simvastatin 80 and 160 mg/day.

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Journal:  Am J Cardiol       Date:  1997-01-01       Impact factor: 2.778

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9.  Comparative efficacy and safety of pravastatin and cholestyramine alone and combined in patients with hypercholesterolemia. Pravastatin Multicenter Study Group II.

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Journal:  Arch Intern Med       Date:  1993-06-14

10.  Reduction of LDL cholesterol by 25% to 60% in patients with primary hypercholesterolemia by atorvastatin, a new HMG-CoA reductase inhibitor.

Authors:  J W Nawrocki; S R Weiss; M H Davidson; D L Sprecher; S L Schwartz; P J Lupien; P H Jones; H E Haber; D M Black
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  8 in total

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Authors:  Q Feng; W Q Wei; C P Chung; R T Levinson; L Bastarache; J C Denny; C M Stein
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2.  [Cost analysis and degree of hypercholesterolemia control in type 2 diabetic patients according to different groups and scientific societies].

Authors:  S Narejos; J Espinàs; A Rodríguez; R M Salla; C Blay; A Puente; M Cantero; J Alsina; M C López
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Review 3.  Pharmacokinetic-pharmacodynamic drug interactions with HMG-CoA reductase inhibitors.

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Review 4.  Clinical pharmacokinetics of cerivastatin.

Authors:  W Mück
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Review 5.  Severe rhabdomyolysis associated with the cerivastin-gemfibrozil combination therapy: report of a case.

Authors:  T K Lau; D R Leachman; R Lufschanowski
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Review 6.  Cerivastatin: a review of its pharmacological properties and therapeutic efficacy in the management of hypercholesterolaemia.

Authors:  G L Plosker; C I Dunn; D P Figgitt
Journal:  Drugs       Date:  2000-11       Impact factor: 9.546

Review 7.  Rational assessment of the interaction profile of cerivastatin supports its low propensity for drug interactions.

Authors:  W Mück
Journal:  Drugs       Date:  1998       Impact factor: 9.546

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  8 in total

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