A 12-Month, Double-Blind, Placebo-Controlled, Parallel-Group Study to Evaluate the Efficacy and Safety of Reslizumab (3.0 mg/kg) in the Reduction of Clinical Asthma Exacerbations in Patients (12-75 Years of Age) With Eosinophilic Asthma

Trial Profile

A 12-Month, Double-Blind, Placebo-Controlled, Parallel-Group Study to Evaluate the Efficacy and Safety of Reslizumab (3.0 mg/kg) in the Reduction of Clinical Asthma Exacerbations in Patients (12-75 Years of Age) With Eosinophilic Asthma

Completed
Phase of Trial: Phase III

Latest Information Update: 06 Jul 2017

At a glance

  • Drugs Reslizumab (Primary)
  • Indications Asthma; Eosinophilia
  • Focus Registrational; Therapeutic Use
  • Acronyms BREATH
  • Sponsors Teva Branded Pharmaceutical Products R&D
  • Most Recent Events

    • 06 Jul 2017 According to a Teva Pharmaceutical Industries media release, based on the data from two phase III studies (3082 and 3083), the German Federal Joint Committee (G-BA) has confirmed that CINQAERO provides evidence for a minor additional benefit in patients with severe eosinophilic asthma who were treated regularly with corticosteroids in addition to the treatment for acute exacerbations.
    • 24 May 2017 Results of a pooled post-hoc analysis assessing the impact of reslizumab treatment on healthcare resource utilization in patients from two phase III, 52-week trials (BREATH program; n=953) presented at the 113th International Conference of the American Thoracic Society
    • 17 May 2017 According to a Teva Pharmaceutical Industries media release, results of pooled post hoc analysis from this and another phase III study (profile 700194191 ) will be presented at the 2017 American Thoracic Society (ATS) International Conference.
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