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Clinical Trials/NCT01119937
NCT01119937
Completed
Phase 3

A 52-week Treatment, Multi-center, Randomized, Open Label, Parallel Group Study to Assess the Long Term Safety and Tolerability of NVA237 (50µg o.d.) Using Tiotropium (18µg o.d.) as an Active Control in Japanese Patients With Moderate to Severe Chronic Obstructive Pulmonary Disease

Novartis Pharmaceuticals1 site in 1 country211 target enrollmentMay 2010

Overview

Phase
Phase 3
Intervention
NVA237
Conditions
Chronic Obstructive Pulmonary Disease
Sponsor
Novartis Pharmaceuticals
Enrollment
211
Locations
1
Primary Endpoint
Number of Participants With Adverse Events, Serious Adverse Events or Death
Status
Completed
Last Updated
13 years ago

Overview

Brief Summary

This is a 52-week, multi-center, randomized, open label, parallel group study to assess the long term safety and tolerability of once-daily NVA237, using tiotropium as an active control, in Japanese patients with moderate to severe chronic obstructive pulmonary disease (COPD) .

Registry
clinicaltrials.gov
Start Date
May 2010
End Date
November 2011
Last Updated
13 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Patients with moderate to severe stable COPD (Stage II or Stage III) according to the Gold Guideline
  • Current or ex-smokers who have a smoking history of at least 10 pack years.
  • Patients with a post-bronchodilator FEV1 ≥30% and \< 80% of the predicted normal, and postbronchodilator FEV1/FVC \< 0.7 at Visit 2 (day -7)

Exclusion Criteria

  • Pregnant women or nursing mothers or women of child-bearing potential not using an acceptable method of contraception
  • Patients requiring long term oxygen therapy
  • Patients who have had a lower respiratory tract infection within 6 weeks prior to Visit 1
  • Patients with concomitant pulmonary disease
  • Patients with a history of asthma
  • Any patient with lung cancer or a history of lung cancer
  • Patients with a history of certain cardiovascular comorbid conditions
  • Patients with a known history and diagnosis of alpha-1 antitrypsin deficiency
  • Patients in the active phase of a supervised pulmonary rehabilitation program
  • Patients contraindicated for tiotropium or ipratropium treatment or who have shown an untoward reaction to inhaled anticholinergic agents

Arms & Interventions

NVA237

50µg once daily

Intervention: NVA237

Tiotropium

18µg once daily

Intervention: Tiotropium

Outcomes

Primary Outcomes

Number of Participants With Adverse Events, Serious Adverse Events or Death

Time Frame: 52 weeks

Adverse events are defined as any unfavorable and unintended diagnosis, symptom, sign (including an abnormal lab finding), syndrome or disease which either occurs during study, having been absent at baseline, or, if present at baseline, appears to worsen. Serious adverse events are any untoward medical occurrences that result in death, are life threatening, require (or prolong) hospitalization, cause persistent or significant disability/incapacity, result in congenital anomalies or birth defects, or are other conditions which in judgments of the investigators represent significant hazards.

Secondary Outcomes

  • Change in Pre-dose FEV1 From Baseline(Weeks 12, 24, 36 and 52)
  • Time From Randomization Until the Start of the First Moderate or Severe COPD Exacerbation(52 weeks)
  • Number of Patients With Newly Occurring or Worsening Clinically Notable Vital Signs Values at Any Timepoint Over the Whole Treatment Period(52 weeks)
  • Change in Pre-dose FVC From Baseline(Weeks 12, 24, 36 and 52)
  • Number of Patients With Moderate or Severe COPD Exacerbations(52 weeks)
  • Change in St. George Respiratory Questionnaire From Baseline(Weeks 12, 24, 36, 52)
  • Change From Baseline in Mean Daily Number of Puffs of Rescue Medication Over the Whole Treatment Period(52 weeks)
  • Number of Patients With Newly Occurring or Worsening Clinically Notable Hematology Values at Any Timepoint Over the Whole Treatment Period(52 weeks)
  • Number of Patients With Newly Occurring or Worsening Clinically Notable Biochemistry Values at Any Timepoint Over the Whole Treatment Period(52 weeks)
  • Number of Patients With Notable Change From Baseline in Fridericia's QTc Values at Any Timepoint Over the Whole Treatment Period(52 weeks)

Study Sites (1)

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