This site is intended for health professionals only

Published on 19 June 2007

Share this story:
Twitter
LinkedIn

Lumiracoxib “better for blood pressure”

teaser

Novartis has presented data which shows that the Swiss-based firm’s anti-inflammatory COX-2 inhibitor Prexige® (lumiracoxib) has significantly less impact on blood pressure than ibuprofen.

Data presented at the European League Against Rheumatism congress in Barcelona, Spain, shows that patients with osteoarthritis who also have controlled hypertension experienced a slight decrease in average daily blood pressure when treated with Prexige compared to a slight increase in those taking ibuprofen, the commonly used nonsteroidal anti-inflammatory drug. Novartis said that the results are particularly important because around 40% of patients with osteoarthritis also have high blood pressure.

The study was a four-week, multicentre, randomised, double-blind, double-dummy, parallel group trial of 787 hypertensive osteoarthritis patients aged 50 or older with ambulatory blood pressure of 140/90mmHg or below, who were being treated with a antihypertensive. In total, 741 patients completed the study, which compared Prexige 100mg once-daily with ibuprofen 600mg taken three times daily.

At the end of the study, patients on Prexige showed a decrease in mean ambulatory systolic blood pressure of 2.7mmHg compared to a 2.2mmHg increase in patients taking ibuprofen. Mean ambulatory diastolic blood pressure was down by 1.5mmHg in Prexige patients compared to a 0.5mmHg rise in those on the older NSAID.

Prexige is approved for use in certain types of patients with osteoarthritic pain of the knee and hip in more than 50 countries, including countries of the European Union, Canada, and countries in Latin America. Novartis noted that the drug is under review by the FDA for relief of the signs and symptoms of osteoarthritis.

PharmaTimes 15/6/2007

 



Most read




Latest Issue

Be in the know
Subscribe to Hospital Pharmacy Europe newsletter and magazine
Share this story:
Twitter
LinkedIn