Either you have JavaScript disabled or your browser does not support Javascript . To work properly, this page requires JavaScript to be enabled.
How to enable JavaScript in your browser?

A 52-week, Double Blind, Double dummy, Randomized, Multinational, Multicentre, 2-arm Parallel Group, active Controlled Clinical Trial of fixed combination of beclometasone dipropionate plus formoterol fumarate plus Glycopyrronium bromide administered via pMDI (CHF 5993) versus indacaterol/glycopyrronium (Ultibro) via DPI in patients with Chronic Obstructive Pulmonary Disease

Next Previous
Search
Trial Profile

A 52-week, Double Blind, Double dummy, Randomized, Multinational, Multicentre, 2-arm Parallel Group, active Controlled Clinical Trial of fixed combination of beclometasone dipropionate plus formoterol fumarate plus Glycopyrronium bromide administered via pMDI (CHF 5993) versus indacaterol/glycopyrronium (Ultibro) via DPI in patients with Chronic Obstructive Pulmonary Disease

Status: Completed
Phase of Trial: Phase III

Latest Information Update: 06 Nov 2021

Price :
$35 *
Note:
  • Adis is an information provider.
  • Final gross price and currency may vary according to local VAT and billing address.
  • Your purchase entitles you to full access to the information contained in our trial profile at the time of purchase.
  • A link to download a PDF version of the trial profile will be included in your email receipt.

At a glance

  • Drugs Beclometasone/formoterol/glycopyrrolate (Primary) ; Glycopyrrolate/indacaterol
  • Indications Chronic obstructive pulmonary disease
  • Focus Registrational; Therapeutic Use
  • Acronyms TRIBUTE
  • Sponsors Chiesi Farmaceutici

Most Recent Events

  • 19 Sep 2018 Results assessing the quality of life of fixed triple combination of extrafine beclometasone dipropionate, formoterol fumarate and glycopyrronium in chronic obstructive pulmonary disease patients, presented at the 28th Annual Congress of the European Respiratory Society.
  • 19 Sep 2018 Results of post-hoc analysis assessing the efficacy of extrafine BDP/FF/G was superior to IND/GLY for reducing exacerbations in Chronic obstructive pulmonary disease patients, presented at the 28th Annual Congress of the European Respiratory Society.
  • 19 Sep 2018 Results of a stratified safety pooled analysis of fatal adverse events (AEs) comparing extrafine ICS-containing combinations vs ICS-free treatments from TRILOGY, TRINITY and TRIBUTE studies presented at the 28th Annual Congress of the European Respiratory Society

You need to be a logged in or subscribed to view this content Request demo (opens in a new window)

If your organization or you do not have a subscription, try one of the following: If your organization has a subscription, there are several access options, even while working remotely:
  • Working within your organization’s network
  • with username/password or try to via your institution
  • Persisted access using your organization’s identifier stored in your user browser for 90 days
Back to top