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Olodaterol Shows Sustained Improvements in Lung Function in Patients with Moderate to Severe Chronic Obstructive Pulmonary Disease (COPD)
Date:9/8/2013

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(P < 0.0001)In these studies, there was no significant difference in adverse events between the olodaterol treatment arm and the placebo arm.

Reported Adverse Events - Study 1:

  • Olodaterol 5 mcg: 31.7 percent
  • Olodaterol 10 mcg: 33.7 percent
  • Placebo: 34.3 percent
  • Reported Adverse Events - Study 2:

  • Olodaterol 5 mcg: 35.7 percent
  • Olodaterol 10 mcg: 38.9 percent
  • Placebo: 33.9 percent
  • The most common adverse reactions were nasopharyngitis, COPD, cough and dyspnea.

    About the Olodaterol Phase 3 Clinical Program
    Olodaterol's efficacy as a once-daily bronchodilator in patients with COPD is being investigated in a robust clinical trial program, involving more than 3,500 patients with moderate to very severe COPD (stages II, III and IV as defined by the Global Initiative for Chronic Obstructive Lung Disease [GOLD]).

    Olodaterol is being investigated to determine the medicine's efficacy in treating COPD patients and is not currently approved for this indication.

    About COPD
    Chronic obstructive pulmonary disease (COPD) includes chronic bronchitis and emphysema. This disease makes it harder to breathe because less air is able to flow in and out of the lungs. As many as 26 million Americans may have COPD – even those who haven't smoked in years – and nearly half of them remain undiagnosed. COPD is the third leading cause of death in the United States. It kills one person every four minutes in the United States.

    Common symptoms of COPD include shortness of breath and coughing with or without excess mucus.

    Leading Respiratory Forward 
    Through research, treatments and patient-centric support services, the Boehringer Ingelheim lung health portfolio is d
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    SOURCE Boehringer Ingelheim Pharmaceuticals, Inc.
    Copyright©2012 PR Newswire.
    All rights reserved

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