Clinical trial

A Comparison of Symbicort® pMDI 2 x 160/4.5 μg Bid and Symbicort® pMDI 2 x…

NCT00206154 · AstraZeneca, Industry · Completed

Key facts

NCT number NCT00206154
Title A Comparison of Symbicort® pMDI 2 x 160/4.5 μg Bid and Symbicort® pMDI 2 x 80/4.5 μg Bid With Formoterol Turbuhaler®, Budesonide pMDI, the Combination of Formoterol Turbuhaler® and Budesonide pMDI, and Placebo in COPD Patients
Official title A 6-Month Double-Blind, Double-Dummy, Randomized, Parallel Group, Multicenter Efficacy & Safety Study of SYMBICORT® pMDI 2 x 160/4.5 µg & 80/4.5 µg Bid Compared to Formoterol TBH, Budesonide pMDI (& the Combination) & Placebo in COPD Patients
Lead sponsor AstraZeneca, Industry
Status Completed
Phase Phase 3
Study type Interventional
Conditions Chronic Obstructive Pulmonary Disease
Intervention type Drug
Interventions Budesonide/formoterol pMDI, Budesonide pMDI, Formoterol Turbuhaler
Enrollment 1,500
Start date Apr 1, 2005
Completion Dec 1, 2006
First posted Sep 21, 2005
Last update posted Mar 27, 2009
Countries Czechia, Netherlands, Poland, South Africa, United States

At a glance

  • 100–999 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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