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Zafirlukast

Zafirlukast is an oral leukotriene receptor antagonist (LTRA) for the maintenance treatment of asthma. Available as a tablet, it blocks the action of leukotriene C4 on its receptors, thus reducing constriction of the airways, build-up of mucus in the lungs and inflammation of the breathing passages.

Zafirlukast is marketed by AstraZeneca with the brand names Accolate, Accoleit, and Vanticon. It was the first LTRA to be marketed in the USA and is now approved in over 60 countries, including the UK, Japan, Italy, Spain, Canada, Brazil and China.

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Cost Effectiveness Of Inhaled Fluticasone Versus Zafirlukast In Patients Switched From Low Dose Inhaled Corticosteroids - Abstract
From CHEST, 10/1/99 by Richard Stanford

Purpose: Compare cost-effectiveness between fluticasone (FP) 88mg twice daily with oral zafirlukast (ZAF) 20mg twice daily in the treatment of asthma.

Methods: Data from two randomized, double-blind, double-dummy, placebo-controlled clinical trials were analyzed. Subjects' previous treatment included low dose inhaled corticosteroids (ICS) (as defined by the NIH guidelines) and short acting beta2-agonists. The primary efficacy parameter was percent improvement in FEV1. Other efficacy measures were symptom-free days (SFD) and improvement in asthma quality of life (QoL). Health care resources (RU) were collected during each asthma exacerbation, defined as additional treatment for asthma symptoms beyond as needed albuterol. Cost of treatment included study drugs, ER visits, unscheduled physician visits, treatment for drug-related adverse events, oral corticosteroids and rescue albuterol. Drug costs were based on AWP and RU costs were based on published data.

Results: The mean asthma treatment cost was $1.66 per day for patients switched to FP and $2.30 for patients switched to ZAF. Patients switched to FP experienced significantly fewer asthma exacerbations (p [is less than] 0.001), better improvement in FEV1 (p [is less than] 0.001) and greater SFD (p [is less than] 0.001). More patients switched to FP experienced improved QoL compared to patients switched to ZAF (p [is less than] 0.001). Cost-effectiveness ratios were lower for patients switched to FP for each 10% improvement in FEV1 ($4.67 vs $9.89), SFD ($3.35 vs $5.71) and 0.5 improvement in AQLQ ($3.18 vs $6.54) and remained lower after sensitivity analysis.

Conclusion: From a third party payer perspective, FP 88mg twice daily is more cost-effective than ZAF 20mg twice daily in patients switched from low-dose ICS.

Clinical Implications: Switching patients from low-dose ICS to low-dose FP is a more cost-effective alternative than switching to oral ZAF.

Supported by: Glaxo Wellcome, Inc.

Richard Stanford, PharmD, MS(*); J Carranza-Rosenweig, PharmD, MS; B Bowers, PharmD; L Edwards, PhD; P Pepsin, BA, RN and K Rickard, MD. Glaxo Wellcome, Inc, Research Triangle Park, NC.

COPYRIGHT 1999 American College of Chest Physicians
COPYRIGHT 2000 Gale Group

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