About: 26 Week Efficacy, Safety and Tolerability Study of Indacaterol in Patients With Chronic Obstructive Pulmonary Disease (COPD)     Goto   Sponge   NotDistinct   Permalink

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clinical trial

AttributesValues
rdf:type
description
  • assaig clínic (ca)
  • clinical trial (en)
  • clinical trial (en-ca)
  • clinical trial (en-gb)
  • clinical trial (en-us)
  • ensaio clínico (gl)
  • ensayo clínico (es)
  • ensayu clínicu (ast)
  • essai clinique (fr)
  • klinisch onderzoek (nl)
  • клінічне випробування (uk)
rdfs:label
  • 26 Week Efficacy, Safety and Tolerability Study of Indacaterol in Patients With Chronic Obstructive Pulmonary Disease (COPD) (en)
  • 26 Week Efficacy, Safety and Tolerability Study of Indacaterol in Patients With Chronic Obstructive Pulmonary Disease (COPD) (nl)
skos:prefLabel
  • 26 Week Efficacy, Safety and Tolerability Study of Indacaterol in Patients With Chronic Obstructive Pulmonary Disease (COPD) (en)
  • 26 Week Efficacy, Safety and Tolerability Study of Indacaterol in Patients With Chronic Obstructive Pulmonary Disease (COPD) (nl)
name
  • 26 Week Efficacy, Safety and Tolerability Study of Indacaterol in Patients With Chronic Obstructive Pulmonary Disease (COPD) (en)
  • 26 Week Efficacy, Safety and Tolerability Study of Indacaterol in Patients With Chronic Obstructive Pulmonary Disease (COPD) (nl)
title
title
  • A 26-week Treatment, Multicenter, Randomized, Double Blind, Double Dummy, Placebo-controlled, Adaptive, Seamless, Parallel-group Study to Assess the Efficacy, Safety and Tolerability of Two Doses of Indacaterol (Selected From 75, 150, 300 & 600 µg o.d.) in Patients With Chronic Obstructive Pulmonary Disease Using Blinded Formoterol (12 µg b.i.d.) and Open Label Tiotropium (18 µg o.d.) as Active Controls (en)
end time
end time
instance of
instance of
start time
start time
country
country
research site
research site
research intervention
research intervention
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