The Journal of Allergy and Clinical Immunology
Volume 102, Issue 6 , Pages 943-952, December 1998

Improved bronchodilation with levalbuterol compared with racemic albuterol in patients with asthma☆☆★★

Presented in part at the annual meeting of the American Thoracic Society, Chicago, Ill, April 1998.

Denver, Colo, Stockton and Encinitas, Calif, Wilmington, NC, and Marlborough, Mass

Received 3 June 1998; received in revised form 24 August 1998; accepted 27 August 1998.

Abstract 

Background: Racemic albuterol is an equal mixture of (R)-albuterol (levalbuterol), which is responsible for the bronchodilator effect, and (S)-albuterol, which provides no benefit and may be detrimental. Objective: We sought to compare 2 doses of a single enantiomer, levalbuterol (0.63 mg and 1.25 mg), and equivalent amounts of levalbuterol administered as racemic albuterol with placebo in patients with moderate-to-severe asthma. Methods: This was a randomized, double-blind, parallel-group trial. Three hundred sixty-two patients 12 years of age or older were treated with study drug administered by means of nebulization 3 times daily for 28 days. The primary endpoint was peak change in FEV1 after 4 weeks. Results: The change in peak FEV1 response to the first dose in the combined levalbuterol group was significantly greater compared with the combined racemic albuterol group (0.92 and 0.82 L, respectively; P = .03), with similar but nonsignificant results after 4 weeks (0.84 and 0.74 L, respectively). Improvement in FEV1 was similar for levalbuterol 0.63 mg and racemic albuterol 2.5 mg and greatest for levalbuterol 1.25 mg. Racemic albuterol 1.25 mg demonstrated the weakest bronchodilator effect, particularly after chronic dosing. The greatest increase in FEV1 was seen after levalbuterol 1.25 mg, especially in subjects with severe asthma. All active treatments were well tolerated, and β-adrenergic side effects after administration of levalbuterol 0.63 mg were reduced relative to levalbuterol 1.25 mg or racemic albuterol 2.5 mg. At week 4, the predose FEV1 value was greatest in patients who received levalbuterol or placebo when compared with those who received racemic albuterol. The difference was more evident and was statistically significant in patients who were not receiving inhaled corticosteroids. Conclusion: Levalbuterol appears to provide a better therapeutic index than the standard dose of racemic albuterol. These results support the concept that (S)-albuterol may have detrimental effects on pulmonary function. (J Allergy Clin Immunol 1998;102:943-52.)

Keywords:  Asthma, levalbuterol, racemic albuterol, bronchodilators, lung function, S-albuterol

Abbreviations:  AUC: , Area under the curve, ECG: , Electrocardiogram, MDI: , Metered-dose inhaler

 

 From a the National Jewish Medical and Research Center, Denver; b Allergy, Immunology & Asthma Group, Inc, Stockton; c 317 North El Camino Real, Encinitas; d PPD Pharmaco Inc, Wilmington; and e Sepracor Inc, Marlborough.

☆☆ Supported by a grant from Sepracor Inc, Marlborough, Mass.

 Reprint requests: Harold S. Nelson, MD, National Jewish Medical and Research Center, 1400 Jackson St, Denver, CO 80206.

★★ 0091-6749/98 $5.00 + 0  1/1/94588

PII: S0091-6749(98)70332-X

The Journal of Allergy and Clinical Immunology
Volume 102, Issue 6 , Pages 943-952, December 1998