A 52-week treatment, multicenter, randomized, double-blind, double dummy, placebo-controlled, parallel-group study to assess the efficacy, safety and tolerability of indacaterol (300 and 600 microg o.d.) in patients with chronic obstructive pulmonary disease, using formoterol (12 microg b.i.d.) as an active control.

Trial Profile

A 52-week treatment, multicenter, randomized, double-blind, double dummy, placebo-controlled, parallel-group study to assess the efficacy, safety and tolerability of indacaterol (300 and 600 microg o.d.) in patients with chronic obstructive pulmonary disease, using formoterol (12 microg b.i.d.) as an active control.

Completed
Phase of Trial: Phase III

Latest Information Update: 26 Feb 2017

At a glance

  • Drugs Indacaterol (Primary) ; Formoterol
  • Indications Chronic obstructive pulmonary disease
  • Focus Adverse reactions; Registrational; Therapeutic Use
  • Acronyms INVOLVE
  • Sponsors Novartis
  • Most Recent Events

    • 01 Jun 2010 1-year results have been published in Thorax.
    • 16 Sep 2009 Secondary endpoint analysis presented at the 19th Annual Congress of the European Respiratory Society
    • 16 Sep 2009 Results presented at the 19th Annual Congress of the European Respiratory Society
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