Clinical trial

Efficacy and Safety Study of Beclometasone/Formoterol Single Inhaler in Patients…

NCT00476099 · Chiesi Farmaceutici S.p.A., Industry · Completed

Key facts

NCT number NCT00476099
Title Efficacy and Safety Study of Beclometasone/Formoterol Single Inhaler in Patients With COPD
Official title A 48-week, Double Blind, Double Dummy, Randomised, Multinational, Multicentre, 3-arm Parallel Group Clinical Study of "Fixed Combination" Beclometasone Dipropionate Plus Formoterol Fumarate Administered Via pMDI With HFA-134a Propellant Versus "Fixed Combination" Budesonide Plus Formoterol DPI…
Lead sponsor Chiesi Farmaceutici S.p.A., Industry
Status Completed
Phase Phase 3
Study type Interventional
Conditions Chronic Obstructive Pulmonary Disease
Intervention type Drug
Interventions Beclomethasone 100 µg plus formoterol 6 µg (CHF1535) pMDI, Budesonide 200 µg plus formoterol 6 µg DPI, Formoterol 12 µg DPI
Enrollment 828
Start date Dec 1, 2006
Primary completion Aug 1, 2008
Completion Nov 1, 2008
First posted May 21, 2007
Last update posted Oct 29, 2021
Countries France

At a glance

  • 1–9 Study sites
  • No Results posted
  • None Linked FDA submissions

Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.

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Source: U.S. National Library of Medicine (NLM), ClinicalTrials.gov · Source date:

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