Table 3. Rosuvastatin Camparator-Controlled Trials in Patients with Primary Hypercholesterolemia
Study | N | Treatments (dose/day) | Results | |
---|---|---|---|---|
% of LDL-Cholesterol Reduction from Baseline | % of Patients Achieving ATP-II or -III Targets |
|||
Olsson
et al. 200114 Randomized, open-label, comparator- and placebo-controlled trial 6 weeks |
142 | Rosuvastatin 1-40 mg | 34-65 | N/A |
Atorvastatin 10 mg | 44 | |||
Atorvastatin 80 mg | 59 | |||
Placebo | -3.6 | |||
Paoletti et al. 200115 Randomized, double-blind, multi-center, comparatory-controlled trial 12 weeks |
502 | Rosuvastatin 5 mg | 42 | 71 |
Rosuvastatin 10 mg | 49 | 87 | ||
Pravastatin 20 mg | 28 | 53 | ||
Simvastatin 20 mg | 37 | 64 | ||
Brown
et al. 200216 Randomized, double-blind, multi-center, comparator-controlled trial |
Fixed
Dose
Period 12 wks 477 |
Rosuvastatin 5 mg | 39 | 80 |
Rosuvastatin 10 mg | 47 | 90 | ||
Pravastatin 20 mg | 27 | 53 | ||
Simvastatin 20 mg | 35 | 69 | ||
Dose
Titration Period 52 wks 477 |
Rosuvastatin 5-80 mg | 42 | 88 | |
Rosuvastatin 10-80 mg | 48 | 88 | ||
Pravastatin 40 mg | 32 | 60 | ||
Simvastatin 80 mg | 38 | 73 | ||
Olsson
et al. 200217 Randomized, double-blind, multi-center, comparator-controlled trial |
Fixed
Dose
Period 12 wks 412 |
Rosuvastatin 5 mg | 46 | 86 |
Rosuvastatin 10 mg | 50 | 73 | ||
Atorvastatin 10 mg | 39 | 86 | ||
Dose
Titration Period 52 wks 412 |
Rosuvastatin 5-80 mg | 47 | 88 | |
Rosuvastatin 10-80 mg | 53 | 98 | ||
Atorvastatin 80 mg | 44 | 87 | ||
Davidson et al.
200218 Randomized, double-blind, multi-center, comparator- and placebo-controlled trial 12 weeks |
516 | Rosuvastatin 5 mg | 40 | 84 |
Rosuvastatin 10 mg | 43 | 82 | ||
Atorvastatin 10 mg | 35 | 72 | ||
Placebo | 0 | 12 |
Adapted from Olsson AG et al. Am J Cardiol 2001; 88:504-8, Paoletti R et al. J Cardiovasc Risk 2001:8:383-90, Brown WV et al. Am Heart J 2002; 144: 1036-43, Olsson AG et al. Am Heart J 2002;144:1044-51, Davidson M et al. Am J Cardiol 2002;89:268-75.