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A Randomized, Double-blind, Placebo-controlled Study of Tumor Necrosis Factor-α Blockade in Severe Persistent Asthma

Authors :
Sally E, Wenzel
Peter J, Barnes
Eugene R, Bleecker
Jean, Bousquet
William, Busse
Sven-Erik, Dahlén
Stephen T, Holgate
Deborah A, Meyers
Klaus F, Rabe
Adam, Antczak
James, Baker
Ildiko, Horvath
Zsuzsanna, Mark
David, Bernstein
Edward, Kerwin
Rozsa, Schlenker-Herceg
Kim Hung, Lo
Rosemary, Watt
Elliot S, Barnathan
Pascal, Chanez
E H, Bel
AII - Amsterdam institute for Infection and Immunity
Pulmonology
Source :
American journal of respiratory and critical care medicine, 179(7), 549-558. American Thoracic Society
Publication Year :
2009
Publisher :
American Thoracic Society, 2009.

Abstract

Rationale The treatment effect of golimumab, a human monoclonal antibody against tumor necrosis factor (TNF)-alpha, in severe persistent asthma is unknown. Objectives To assess the safety and efficacy of golimumab in a large population of patients with uncontrolled, severe persistent asthma. Methods From 2004 to 2006, 309 patients with severe and uncontrolled asthma, despite high-dose inhaled corticosteroids and long-acting beta(2) agonists, were randomized 1:1:1:1 to monthly subcutaneous injections of placebo or golimumab (50, 100, or 200 mg) through Week 52. Coprimary endpoints were the change from baseline through Week 24 in prebronchodilator percent-predicted FEV(1) and the number of severe asthma exacerbations through Week 24. Measurements and main results No significant differences were observed for the change in percent-predicted FEV1 (least squares mean: placebo, 2.44 [95% confidence interval (CI) -0.574 to 5.461]; combined 100-mg and 200-mg, 2.91 [0.696-5.116]) or severe exacerbations (mean +/- SD: placebo, 0.5 +/- 1.07 vs. combined 100-mg and 200-mg 0.5 +/- 0.97) through week 24. Through Week 24, 2.6% of patients treated with placebo vs. 19.5% of those treated with golimumab discontinued the study agent, and 1.3% and 7.8% discontinued study participation, respectively. An unfavorable risk-benefit profile led to early discontinuation of study-agent administration after the Week-24 database lock. Through Week 76, 20.5% of patients treated with placebo and 30.3% of patients treated with golimumab experienced serious adverse events, with serious infections occurring more frequently in golimumab-treated patients. One death and all eight malignancies occurred in the active groups. Conclusions Overall, treatment with golimumab did not demonstrate a favorable risk-benefit profile in this study population of patients with severe persistent asthma. Clinical trial registered with www.clinicaltrials.gov (NCT00207740).

Details

ISSN :
15354970 and 1073449X
Volume :
179
Database :
OpenAIRE
Journal :
American Journal of Respiratory and Critical Care Medicine
Accession number :
edsair.doi.dedup.....96c0f2c63111182d318d3bd90337039f
Full Text :
https://doi.org/10.1164/rccm.200809-1512oc