Efficacy of NVA237 (50 μg o.d) Using Tiotropium (5μg μg o.d) as Active Control in COPD Patients.

Pulmonary Disease, Chronic Obstructive Clinical Trial

Official title:

A 52-week Treatment, Multi-center, Randomized, Open Label, Parallel Group Study to Assess the Efficacy of NVA237 (50 μg o.d.) Using Tiotropium (5 μg o.d.) as an Active Control in Brazilian Patients With Moderate to Severe Chronic Obstructive Pulmonary Disease.

Clinical Trial Details — Status: Withdrawn

Administrative data

• NCT number: NCT01837927
• Other study ID #: CNVA237ABR01
• Status: Withdrawn
• Phase: Phase 3
• First received: April 18, 2013
• Last updated: August 19, 2016
• Start date: April 2014
• Est. completion date: April 2016

Study information

• Verified date: August 2016
• Source: Novartis
• Contact: n/a
• Is FDA regulated: No
• Health authority: ANVISA BRAZIL ':' (Brazilian Health Surveillance Agency)
• Study type: Interventional

Clinical Trial Summary

This study will assess the Efficacy of NVA237 (50 μg o.d) using tiotropium (5μg μg o.d) as active control in COPD patients.

Description:

A 52-week treatment, multicenter, randomized, open-label, parallel-group study to assess the efficacy of NVA237 (50μg once daily) using Tiotropium (5μg once daily) as an active control in Brazilian patients with moderate to severe Chronic Obstructive Pulmonary Disease.

Recruitment information / eligibility

• Status: Withdrawn
• Enrollment: 0
• Est. completion date: April 2016
• Est. primary completion date: April 2016
• Accepts healthy volunteers: No
• Gender: Both
• Age group: 40 Years and older

Eligibility

Inclusion:

• Men and women aged 40 years or over.

• History of current or former smoking of at least 10 pack-years

• Cooperative outpatients, with a COPD diagnosis established by the measurement of FEV1/FVC < 0.7 post-bronchodilation in basal spirometry (without use of medication or post-washout). Moderate to severe stage patients will be included, with post-bronchodilator FEV1 between 30 and 80% of the normal value according to GOLD 2011 since the inclusion criteria in this trial will be based on spirometry results.

Exclusion:

• Pregnant women or nursing mothers

• History of asthma at visit 1 indicated by, but not limited to:

• Onset of respiratory symptoms suggestive of asthma (such as coughing, wheezing, shortness of breath) before the age of 40.

• History of diagnosed asthma

• History of respiratory tract infection within six weeks prior to Visit 1.

• History of hospitalization or emergency care for a COPD exacerbation in the 3 months prior to Visit 1.

• Subjects who require use of home oxygen therapy.

• Patients in the active phase of an assisted pulmonary rehabilitation program and patients who completed the rehabilitation program within 18 months from Visit 1 or 2 of the protocol.17,20

• Patients with known history and diagnosis of alpha-1 antitrypsin deficiency.

• Patients with concomitant lung disease, e.g.: tuberculosis (unless confirmed by radiography as inactive) or clinically significant bronchiectasis.

• Patients who in the investigator's judgment have an abnormality or significant medical condition such as: unstable ischemic heart disease, left ventricular failure, history of myocardial infarction, arrhythmia (except chronic stable atrial fibrillation), history of malignancy of any system (including lung cancer) treated or not within the last 5 years, glaucoma, prostatic hyperplasia, moderate to severe renal impairment, urinary retention, any other condition that might compromise patient safety or compliance, interfere with the evaluations, or prevent the termination of their participation in the study.

• Patients with contraindications to tiotropium or ipratropium treatment or who have experienced undesirable reactions with inhaled anticholinergic agents or patients with a history of an undesirable reaction with sympathomimetic amines or inhaled medication with any of those components, or a history of hypersensitivity to any of the study medications, including rescue medication, or similar classes of medication.

• Patients using tiotropium, long-acting anticholinergics, short-acting anticholinergics, fixed combinations of inhaled beta agonists and inhaled corticosteroids, theophylline. In these cases, the patient is allowed, after agreeing to participate in the study, to enter a washout period from Visit

• Patients using inhaled steroids, alone or as an exchange in a fixed combination at equivalent doses, unless on a stable treatment for at least 1 month prior to randomization

• Patients using nonselective beta-blockers.

• Patients using cromoglycate, nedocromil, ketotifen and leukotriene antagonists unless on stable treatment for at least 1 month prior to randomization .

• Patients who used oral prednisone (or equivalent) over a long period, defined as = 10 mg/day for at least 1 month prior to Visit 1

• Patients who used intramuscular depot corticosteroids within 30 days from Visit 1.

• Patients with a history of long QT Syndrome or with prolonged QTc (> 450 ms) measured at Visit 1 (Fridericia Method).

• Patients who, in the opinion of the investigator, have clinically significant abnormalities on ECG. These patients should not be re-screened.

• Other exclusion criteria may apply

Study Design

Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Treatment

Related Conditions & MeSH terms

• Chronic Disease
• Lung Diseases
• Lung Diseases, Obstructive
• Pulmonary Disease, Chronic Obstructive

Intervention

Drug:
• NVA237
Once daily for 52 weeks
• Tiotropium Respimat®
Once daily for 52 weeks

Locations

Country	Name	City	State
n/a

Sponsors (1)

Lead Sponsor	Collaborator
Novartis Pharmaceuticals

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Change From Baseline in Forced Expiratory Volume in 1 Second (FEV1)	Forced expiratory volume in 1 second (FEV1) is the amount of air that can be exhaled in one second. FEV1 will be measured by spirometry. A positive change from baseline in FEV1 indicates improvement in lung function.	Baseline and 12 weeks after treatment.	No
Secondary	Forced Expiratory Volume in 1 Second (FEV1) at day 1	Forced expiratory volume in 1 second (FEV1) is the amount of air that can be exhaled in one second. FEV1 will be measured by spirometry. A positive change from baseline in FEV1 indicates improvement in lung function.	30 and 60 minutes post-dose on the first day of study treatment.	No
Secondary	Forced Expiratory Volume in 1 Second (FEV1) at day 7 and weeks 12, 24 and 52	Forced expiratory volume in 1 second (FEV1) is the amount of air that can be exhaled in one second. FEV1 will be measured by spirometry. A positive change from baseline in FEV1 indicates improvement in lung function.	30 and 60 minutes post-dose on the 7th day of study treatment and at weeks 12, 24 and 52	No
Secondary	Forced Expiratory Volume in 1 Second (FEV1) at weeks 24 and 52	Forced expiratory volume in 1 second (FEV1) is the amount of air that can be exhaled in one second. FEV1 will be measured by spirometry. A positive change from baseline in FEV1 indicates improvement in lung function.	pre-dose at weeks 24 and 52 of study treatment	No
Secondary	Change From Baseline in Forced Vital Capacity (FVC)	Forced Vital Capacity (FVC) is the amount of air which can be forcibly exhaled from the lungs after taking the deepest breath possible. FVC was assessed via spirometry. A positive change from baseline in FVC indicates improvement in lung function.	Days 1 and 7, weeks 12, 24 and 52 of study treatment	No
Secondary	FEV1 AUC 0-4h	Forced Vital Capacity (FVC) is the amount of air which can be forcibly exhaled from the lungs after taking the deepest breath possible. FVC was assessed via spirometry. A positive change from baseline in FVC indicates improvement in lung function.	05, 30, 60 minutes and 4 hours post-dose at days 1, 7 and week 12	No
Secondary	Safety and tolerance of NVA237	All AEs and SAEs will be reported	52 weeks	Yes