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A Randomised, Double Blind, Parallel Group Study to Assess the Efficacy and Safety of 12 Weeks of Once Daily, Orally Inhaled, Co-administration of Olodaterol 5microg (Delivered by the Respimat Inhaler) and Tiotropium 18microg (Delivered by the HandiHaler) Compared to Once Daily, Orally Inhaled, Co-administration of Placebo (Delivered by the Respimat Inhaler) and Tiotropium 18microg (Delivered by the HandiHaler) in Patients With Chronic Obstructive Pulmonary Disease (COPD) [ANHELTO 2]

Trial Profile

A Randomised, Double Blind, Parallel Group Study to Assess the Efficacy and Safety of 12 Weeks of Once Daily, Orally Inhaled, Co-administration of Olodaterol 5microg (Delivered by the Respimat Inhaler) and Tiotropium 18microg (Delivered by the HandiHaler) Compared to Once Daily, Orally Inhaled, Co-administration of Placebo (Delivered by the Respimat Inhaler) and Tiotropium 18microg (Delivered by the HandiHaler) in Patients With Chronic Obstructive Pulmonary Disease (COPD) [ANHELTO 2]

Status: Completed
Phase of Trial: Phase III

Latest Information Update: 20 May 2015

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At a glance

  • Drugs Olodaterol (Primary) ; Tiotropium bromide
  • Indications Chronic obstructive pulmonary disease
  • Focus Registrational; Therapeutic Use
  • Acronyms ANHELTO 2
  • Sponsors Boehringer Ingelheim Pharmaceuticals
  • Most Recent Events

    • 01 Oct 2013 Status changed from active, no longer recruiting to completed as reported by ClinicalTrials.gov.
    • 26 Jun 2013 Status changed from recruiting to active, no longer recruiting as reported by ClinicalTrials.gov.
    • 08 Oct 2012 New trial record
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