A 26-week Multi-center Randomized Double-blind Study to Compare Efficacy and Safety of NVA237 Versus Placebo as an add-on to Maintenance Therapy With Fixed-dose Combination Salmeterol/Fluticasone Propionate in COPD Patients With Moderate to Severe Airflow Limitation

Trial Profile

A 26-week Multi-center Randomized Double-blind Study to Compare Efficacy and Safety of NVA237 Versus Placebo as an add-on to Maintenance Therapy With Fixed-dose Combination Salmeterol/Fluticasone Propionate in COPD Patients With Moderate to Severe Airflow Limitation

Withdrawn prior to enrolment
Phase of Trial: Phase III

Latest Information Update: 25 Apr 2017

At a glance

  • Drugs Glycopyrrolate (Primary) ; Salmeterol/fluticasone propionate
  • Indications Chronic obstructive pulmonary disease
  • Focus Registrational; Therapeutic Use
  • Acronyms GLOW-8
  • Sponsors Novartis Pharmaceuticals
  • Most Recent Events

    • 11 Mar 2013 Status changed from recruiting to withdrawn prior to recruitment as reported by European Clinical Trials Database.
    • 23 Feb 2013 New source identified and integrated (European Clinical Trials Database: EudraCT2012-002854-21).
    • 19 Feb 2013 Status changed from not yet recruiting to recruiting as reported by European Clinical Trials Database.
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