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Regulatory Requisite Post Marketing Surveillance to Assess the Safety and Efficacy of Spiriva HandiHaler (Tiotropium Bromide Inhalation Powder 18mcg, q.d.) in Korean COPD Patients: A 30-Day, Open Label, Non-interventional Study

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Trial Profile

Regulatory Requisite Post Marketing Surveillance to Assess the Safety and Efficacy of Spiriva HandiHaler (Tiotropium Bromide Inhalation Powder 18mcg, q.d.) in Korean COPD Patients: A 30-Day, Open Label, Non-interventional Study

Status: Completed
Phase of Trial: Phase IV

Latest Information Update: 21 Nov 2013

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At a glance

  • Drugs Tiotropium bromide (Primary)
  • Indications Chronic obstructive pulmonary disease
  • Focus Adverse reactions
  • Sponsors Boehringer Ingelheim Pharmaceuticals

Most Recent Events

  • 04 Nov 2009 Actual end date (Dec 2007) added as reported by ClinicalTrials.gov.
  • 04 Nov 2009 Actual patient number (3021) added as reported by ClinicalTrials.gov.
  • 04 Nov 2009 Status changed from active, no longer recruiting to completed as reported by ClinicalTrials.gov record.

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