Archived: ranolazine (Ranexa)
Advice
Following a full submission
ranolazine (Ranexa) is not recommended for use within NHS Scotland 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 after 12 weeks compared with placebo. However, the effect size was small.
The manufacturer did not present a sufficiently robust economic analysis to gain acceptance by SMC.
The licence holder has indicated their intention to resubmit
Drug Details
| Drug Name: | ranolazine (Ranexa) |
|---|---|
| SMC Drug ID: | 565/09 |
| Manufacturer: | A Menarini Pharmaceuticals UK Ltd |
| Indication: | Symptomatic treatment of patients with stable angina pectoris |
| BNF Category: | |
| Sub Category: | 2.6 Nitrates*** calcium-channel blockers*** and other antianginal drugs |
| Submission Type: | Full submission |
| Status: | Not Recommended |
| Date Advice Published: | 7 September 2009 |
Current Advice
| ranolazine (Ranexa) | Resubmission | 16 January 2012 |
Archived Advice
| ranolazine (Ranexa) Resubmission | Resubmission | 13 December 2010 |