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Randomised, Double-Blind, Active Controlled, 3-Arm Parallel Group, Multi-National, Multi-Centre Study to Evaluate the Cardiac Safety of Two Doses of Glycopyrrolate Bromide (25 microG AND 50 microG BID) Delivered Via HFA PMDI Both Combined with Foster 100/6 microG BID Delivered Via HFA PMDI Versus Foster 100/6 microG BID Delivered Via HFA PMDI in Patients with Moderate to Severe Chronic Obstructive Pulmonary Disease

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Trial Profile

Randomised, Double-Blind, Active Controlled, 3-Arm Parallel Group, Multi-National, Multi-Centre Study to Evaluate the Cardiac Safety of Two Doses of Glycopyrrolate Bromide (25 microG AND 50 microG BID) Delivered Via HFA PMDI Both Combined with Foster 100/6 microG BID Delivered Via HFA PMDI Versus Foster 100/6 microG BID Delivered Via HFA PMDI in Patients with Moderate to Severe Chronic Obstructive Pulmonary Disease

Status: Completed
Phase of Trial: Phase II

Latest Information Update: 07 Nov 2021

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At a glance

  • Drugs Beclometasone/formoterol (Primary) ; Beclometasone/formoterol/glycopyrrolate (Primary) ; Beclometasone/formoterol/glycopyrrolate (Primary)
  • Indications Chronic obstructive pulmonary disease
  • Focus Therapeutic Use
  • Acronyms CARSAF
  • Most Recent Events

    • 09 Oct 2012 Planned end date changed from 1 Feb 2013 to 1 Jan 2013 as reported by ClinicalTrials.gov record.
    • 24 Apr 2012 Additional lead trial investigator identified as reported by ClinicalTrials.gov.
    • 24 Apr 2012 Planned end date changed from 29 Dec 2012 to 1 Feb 2013 as reported by ClinicalTrials.gov.

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