Multiple Dose Comparison of Tiotropium Inhalation Capsules, Salmeterol Inhalation Aerosol and Placebo in Patients With Chronic Obstructive Pulmonary Disease (COPD)

NCT ID: NCT02172287

Last Updated: 2014-06-24

Basic Information

• Recruitment Status: COMPLETED
• Clinical Phase: PHASE3
• Total Enrollment: 623 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 1999-02-28

Brief Summary

To compare the long -term (six month) bronchodilator efficacy and safety of tiotropium inhalation capsules, salmeterol inhalation aerosol and placebo in patients with COPD. A secondary objective of this study was to compare the impact of tiotropium and salmeterol on humanistic and economic health outcomes, such as quality of life, patient preference and Health Resource Utilisation in this patient population.

Conditions

Pulmonary Disease, Chronic Obstructive

Study Design

• Allocation Method: RANDOMIZED
• Intervention Model: PARALLEL
• Primary Study Purpose: TREATMENT
• Blinding Strategy: DOUBLE

Study Groups

Tiotropium (Ba679 BR)

Tiotropium capsule once daily by oral inhalation

Group Type: EXPERIMENTAL

Tiotropium (Ba679 BR)

Intervention Type: DRUG

One capsule once daily by oral inhalation

Placebo (for Salmeterol)

Intervention Type: DRUG

Placebo for Salmeterol delivered by inhalation aerosol

Salmeterol

Salmeterol inhalation aerosol twice daily

Group Type: ACTIVE_COMPARATOR

Salmeterol

Intervention Type: DRUG

Inhalation aerosol twice daily

Placebo (for Tiotropium )

Intervention Type: DRUG

Placebo for Tiotropium delivered by inhalation capsule

Placebo

• Tiotropium (Ba679 BR)- placebo one capsule once daily by inhalation
• Salmeterol- placebo, inhalation aerosol twice daily

Group Type: PLACEBO_COMPARATOR

Placebo (for Tiotropium )

Intervention Type: DRUG

Placebo for Tiotropium delivered by inhalation capsule

Placebo (for Salmeterol)

Intervention Type: DRUG

Placebo for Salmeterol delivered by inhalation aerosol

Interventions

Tiotropium (Ba679 BR)

One capsule once daily by oral inhalation

Intervention Type: DRUG

Salmeterol

Inhalation aerosol twice daily

Intervention Type: DRUG

Placebo (for Tiotropium )

Placebo for Tiotropium delivered by inhalation capsule

Intervention Type: DRUG

Placebo (for Salmeterol)

Placebo for Salmeterol delivered by inhalation aerosol

Intervention Type: DRUG

Eligibility Criteria

Inclusion Criteria

1. Age ≥ 40 years.

2. A diagnosis of relatively stable, moderate to severe COPD with:

3. Screening FEV1 ≤ 60% of predicted normal value (calculated according to European Community for Coal and Steel (ECCS criteria R94- R1408) and screening FEV1 ⁄ FVC ≤ 70%).

4. Smoking history ≥ 10 pack-years (a pack-year is 20 cigarettes per day for one year or equivalent).

5. Ability to be trained in the proper use of the HandiHaler® device and Mahler Dyspnoea Index (MDI).

6. Ability to perform all study related tests including the Shuttle Walking Test, acceptable pulmonary function tests, including Peak Expiratory Flow Rate (PEFR) measurements, and maintenance of daily diary card records.

7. Ability to give written informed consent in accordance with Good Clinical Practice (GCP) and local regulations.

Exclusion Criteria

1. Clinically significant diseases other than COPD. A clinically significant disease is defined as one which in the opinion of the investigator may either put the patient at risk because of participation in the study or a disease which may influence the results of the study or the patient's ability to participate in the study.

2. Patients with clinically relevant abnormal baseline haematology, blood chemistry or urinalysis, if the abnormality defines a disease listed as an exclusion criterion, will be excluded.

3. All patients with a serum glutamic oxaloacetic transaminase (SGOT) > 80 IU/L, serum glutamic pyruvic transaminase (SGPT) > 80 IU/L, bilirubin > 2.0 mg/dL or creatinine > 2.0 mg/dL will be excluded regardless of clinical condition. Repeat laboratory evaluation should have not been conducted in these patients.

4. A recent history (i.e., one year or less) of myocardial infarction.

5. Any cardiac arrhythmia requiring drug therapy or hospitalisation for heart failure within the past three years.

6. Inability to abstain from regular daytime use of oxygen therapy for more than 1 hour per day.

7. Known active tuberculosis.

8. History of cancer within the last five years (excluding basal cell carcinoma).

9. History of life-threatening pulmonary obstruction, or a history of cystic fibrosis or bronchiectasis.

10. Patients who have undergone thoracotomy with pulmonary resection.

11. Any upper respiratory infection in the past six weeks prior to the screening visit or during the run-in period.

12. Current participation in a pulmonary rehabilitation programme or completion of a pulmonary rehabilitation programme in the six week prior to the screening visit.

13. Known hypersensitivity to anticholinergic drugs, salmeterol, or any of the components of the lactose powder capsule or MDI delivery systems.

14. Known symptomatic prostatic hypertrophy or bladder neck obstruction.

15. Patients with known narrow-angle glaucoma.

16. Current treatment with cromolyn sodium or nedocromil sodium.

17. Current treatment with antihistamines (H1 receptor antagonists).

18. Oral corticosteroids medication at unstable doses (i.e. less than six weeks on a stable dose) or at doses in excess of the equivalent of 10 mg prednisolone per day or 20 mg every other day.

19. Current use of β-blocker medication.

20. Current treatment with monoamine oxidase inhibitors of tricyclic and antidepressants.

21. Pregnant or nursing women or women of childbearing potential not using a medically approved means of contraception.

22. Patients with a history of asthma, allergic rhinitis or atopy or who have a total blood eosinophil count ≥ 600 mm3. A repeat eosinophil count was not permitted.

23. History of and/or active significant alcohol or drug abuse.

24. Concomitant or recent use of an investigational drug within one month or six half lives (whichever is greater) prior to the screening visit.

25. Changes in the pulmonary therapeutic plan within the six weeks prior to the screening visit.

26. Inability to comply with the medication restrictions specified in Section 4.2 of the trial protocol.

• Minimum Eligible Age: 40 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

Boehringer Ingelheim

INDUSTRY

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Other Identifiers

205.130

Identifier Type: -

Identifier Source: org_study_id