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A Randomized, Double-Blind, Parallel Group, 52-Week Study to Compare the Effect of Fluticasone Propionate/Salmeterol Diskus Combination Product 250/50mcg BID With Salmeterol Diskus 50mcg BID on the Annual Rate of Moderate/Severe Exacerbations in Subjects With Chronic Obstructive Pulmonary Disease

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A Randomized, Double-Blind, Parallel Group, 52-Week Study to Compare the Effect of Fluticasone Propionate/Salmeterol Diskus Combination Product 250/50mcg BID With Salmeterol Diskus 50mcg BID on the Annual Rate of Moderate/Severe Exacerbations in Subjects With Chronic Obstructive Pulmonary Disease

Status: Completed
Phase of Trial: Phase IV

Latest Information Update: 07 Sep 2023

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At a glance

  • Drugs Salmeterol (Primary) ; Salmeterol/fluticasone propionate (Primary)
  • Indications Chronic obstructive pulmonary disease
  • Focus Therapeutic Use
  • Sponsors GSK

    • Most Recent Events

    • 01 Oct 2009 Primary endpoint 'Symptom exacerbation rate' has been met.
    • 17 May 2009 Cost-effectiveness results reported at the 105th International Conference of the American Thoracic Society (ATS) 2009.
    • 18 May 2008 Primary endpoint achieved; results reported at the International Conference of the American Thoracic Society according to a GlaxoSmithKline media release.

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