A 26-week treatment, multi-center, randomized, double-blind, double- dummy, placebo-controlled, parallel-group study to assess the efficacy, and safety of indacaterol (150 microg o.d.) in patients with chronic obstructive pulmonary disease, using salmeterol (50 microg b.i.d.) as an active control.

Trial Profile

A 26-week treatment, multi-center, randomized, double-blind, double- dummy, placebo-controlled, parallel-group study to assess the efficacy, and safety of indacaterol (150 microg o.d.) in patients with chronic obstructive pulmonary disease, using salmeterol (50 microg b.i.d.) as an active control.

Completed
Phase of Trial: Phase III

Latest Information Update: 05 Mar 2018

At a glance

  • Drugs Indacaterol (Primary) ; Salmeterol
  • Indications Chronic obstructive pulmonary disease
  • Focus Registrational; Therapeutic Use
  • Acronyms INLIGHT-2
  • Sponsors Novartis
  • Most Recent Events

    • 24 May 2017 Results (n=8445) of a pooled analysis from 11 Phase III/IIIb indacaterol studies assessing the efficacy and safety of once-daily indacaterol 150 and 300 ug in elderly patients with moderate to severe COPD, published in the Respiratory Medicine.
    • 04 Jul 2012 Company added in the association field as reported by EudraCT.
    • 23 Jun 2010 New source identified and integrated (Clinical Trials Registry - India).
Restricted Access

Oops, it looks like you don’t have a valid subscription to this content. To gain full access to the content and functionality of the AdisInsight database try one of the following.

  • with a username/password associated to an account with a valid subscription
  • Contact your organization’s admin about adding this content to your AdisInsight subscription
  • Request a trial

If you are a subscriber to this content then contact us at AsktheExpert.AdisInsight@springer.com so we can help.

Back to top