HZC102970: A 52-week Efficacy and Safety Study to Compare the Effect of Three Dosage Strengths of Fluticasone Furoate/GW642444 Inhalation Powder With GW642444 on the Annual Rate of Exacerbations in Subjects With Chronic Obstructive Pulmonary Disease (COPD).

Trial Profile

HZC102970: A 52-week Efficacy and Safety Study to Compare the Effect of Three Dosage Strengths of Fluticasone Furoate/GW642444 Inhalation Powder With GW642444 on the Annual Rate of Exacerbations in Subjects With Chronic Obstructive Pulmonary Disease (COPD).

Completed
Phase of Trial: Phase III

Latest Information Update: 10 Jul 2017

At a glance

  • Drugs Vilanterol/fluticasone furoate (Primary) ; Vilanterol
  • Indications Chronic obstructive pulmonary disease
  • Focus Registrational; Therapeutic Use
  • Most Recent Events

    • 09 Jan 2012 Primary endpoint 'Symptom-exacerbation-rate' has been met, according to a GlaxoSmithKline and Theravance media release.
    • 21 Dec 2011 Additional locations (Argentina, Chile) added as reported by ClinicalTrials.gov.
    • 04 Nov 2011 Status changed from active, no longer recruiting to completed as reported by ClinicalTrials.gov.
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