ranolazine (Ranexa)
Advice
following a second resubmission
ranolazine (Ranexa®) is not recommended for use within NHS Scotland.
Indication under review: as add-on therapy for the symptomatic treatment of patients with stable angina pectoris who are inadequately controlled or intolerant to first-line antianginal therapies (such as beta-blockers and/or calcium antagonists).
When added to standard doses of antianginal drugs, ranolazine increased exercise duration at trough drug levels compared with placebo after 12 weeks treatment. Although significant the effect size was modest.
The submitting company did not present a sufficiently robust clinical and economic case to gain acceptance by SMC.
Drug Details
| Drug Name: | ranolazine (Ranexa) |
|---|---|
| SMC Drug ID: | 565/09 |
| Manufacturer: | A Menarini Pharmaceuticals UK Ltd |
| Indication: | as add-on therapy for the symptomatic treatment of patients with stable angina pectoris who are inadequately controlled or intolerant to first-line anti-anginal therapies (such as beta-blockers and/or calcium channel blockers [CCB]) [1]. |
| BNF Category: | |
| Sub Category: | 2.6 Nitrates calcium-channel blockers and other antianginal drugs |
| Submission Type: | Resubmission |
| Status: | Not Recommended |
| Date Advice Published: | 16 January 2012 |
Archived Advice
| ranolazine (Ranexa) Resubmission | Resubmission | 13 December 2010 |
| ranolazine (Ranexa) | Full submission | 7 September 2009 |