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Mepolizumab or Placebo for Eosinophilic Granulomatosis with Polyangiitis
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Mepolizumab or Placebo for Eosinophilic Granulomatosis with Polyangiitis
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Mepolizumab or Placebo for Eosinophilic Granulomatosis with Polyangiitis
Mepolizumab or Placebo for Eosinophilic Granulomatosis with Polyangiitis

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Mepolizumab or Placebo for Eosinophilic Granulomatosis with Polyangiitis
Mepolizumab or Placebo for Eosinophilic Granulomatosis with Polyangiitis
Journal Article

Mepolizumab or Placebo for Eosinophilic Granulomatosis with Polyangiitis

2017
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Overview
Among participants with eosinophilic granulomatosis with polyangiitis, 32% had remission at weeks 36 and 48 when treated with mepolizumab, an anti–interleukin-5 monoclonal antibody, as compared with 3% of the participants in the placebo group. Eosinophilic granulomatosis with polyangiitis (formerly known as the Churg–Strauss syndrome) is characterized by asthma, sinusitis, pulmonary infiltrates, neuropathy, and eosinophilic vasculitis of one or more end-organs. 1 – 4 Eosinophils are thought to induce pathogenic effects in patients with eosinophilic granulomatosis with polyangiitis by means of tissue and vascular infiltration and inflammation through a variety of mediators. 5 , 6 Although systemic glucocorticoids form the cornerstone of treatment for eosinophilic granulomatosis with polyangiitis, 7 – 9 most patients remain dependent on glucocorticoid therapy, and relapses are common. 10 – 13 Furthermore, some patients do not have a sufficient response to glucocorticoids. Because recurrent relapses place the patient at . . .