A Study to Assess the Long-term Safety of QVA149
NCT01120717 · Status: COMPLETED · Phase: PHASE3 · Type: INTERVENTIONAL · Enrollment: 339
Last updated 2013-01-31
Summary
The study is designed to provide long-term safety data for QVA149 in patients with moderate to severe chronic obstructive pulmonary disease (COPD).
Conditions
Interventions
- DRUG
-
QVA149
capsules for inhalation, delivered by an SDDPI
- DRUG
-
capsules for inhalation, delivered by an SDDPI
Sponsors & Collaborators
- lead INDUSTRY
Principal Investigators
-
Novartis Pharmaceuticals · Novartis Pharmaceuticals
Study Design
- Allocation
- RANDOMIZED
- Purpose
- TREATMENT
- Masking
- QUADRUPLE
- Model
- PARALLEL
Eligibility
- Min Age
- 40 Years
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2010-04-30
- Primary Completion
- 2011-12-31
- Completion
- 2011-12-31
Countries
- Canada
- France
- Hungary
- India
- Latvia
- Lithuania
- Romania
- South Africa
- South Korea
- United Kingdom
Study Locations
More Related Trials
-
QVA149 Versus Fluticasone/Salmeterol in Patients With Chronic Obstructive Pulmonary Disease (COPD)
NCT01315249 ·Status: COMPLETED ·Phase: PHASE3
-
A 26-week Treatment Randomized, Double-blind, Double Dummy Study to Assess the Efficacy and Safety of QVA149
NCT01709903 ·Status: COMPLETED ·Phase: PHASE3
-
Comparison of Long-term Safety of the Combination Product QVA149A Against Placebo and Standard of Care Treatment in Chronic Obstructive Pulmonary Disease Patients With Moderate to Severe Airflow Limitation
NCT01610037 ·Status: COMPLETED ·Phase: PHASE3
-
Effect of QVA149 (Indacaterol Maleate/Glycopyrronium Bromide) on Cardiac Function in COPD Patients
NCT02442206 ·Status: COMPLETED ·Phase: PHASE4
-
A Multicenter, 4-week Crossover (Total Duration 12 Weeks) to Determine the Impact of QVA149 on Nocturnal Oxygen Levels in Chronic Obstructive Pulmonary Disease (COPD)
NCT02233543 ·Status: COMPLETED ·Phase: PHASE4
-
Efficacy and Safety Study of Indacaterol Maleate/Glycopyrronium Bromide in Chronic Obstructive Pulmonary Disease (COPD) Patients.
NCT02487498 ·Status: COMPLETED ·Phase: PHASE3
-
Efficacy and Safety Study of QVA149 in COPD Patients
NCT02487446 ·Status: COMPLETED ·Phase: PHASE3
-
A Study to Assess the Safety, Tolerability and Efficacy of NVA237 Versus Placebo
NCT01005901 ·Status: COMPLETED ·Phase: PHASE3
-
Long Term Safety Study of NVA237 vs QAB149 in COPD Patients
NCT01697696 ·Status: COMPLETED ·Phase: PHASE3
-
A Multi-centre Randomized Double Blind 52-week Study to Assess the Safety of QVA149 Compared to QAB149 in Patients With COPD Who Have Moderate to Severe Airflow Limitation
NCT01682863 ·Status: COMPLETED ·Phase: PHASE3
-
The Effect of QVA149 on Health Related Quality of Life in Patients With Chronic Obstructive Pulmonary Disease (COPD)
NCT01574651 ·Status: COMPLETED ·Phase: PHASE3
-
Long Term Safety and Tolerability of QVA149 Versus Tiotropium in Japanese Patients With Chronic Obstructive Pulmonary Disease (COPD)
NCT01285492 ·Status: COMPLETED ·Phase: PHASE3
-
Comparison of Safety and Efficacy of the Combination Product QVA149A Against the Concurrent Administration of the Individual Components, QAB149 and NVA237, in Patients With Chronic Obstructive Pulmonary Disease (COPD)
NCT01529632 ·Status: COMPLETED ·Phase: PHASE3
-
Assessment of Switching From Salmeterol/Fluticasone to Indacaterol/Glycopyrronium in a symtomaticCOPD Patient Cohort
NCT02516592 ·Status: COMPLETED ·Phase: PHASE4
-
Safety and Tolerability of 28 Days Treatment With Glycopyrronium Bromide (NVA237) (100 or 200 µg Once a Day) in Patients With Moderate to Severe Chronic Obstructive Pulmonary Disease
NCT00510510 ·Status: COMPLETED ·Phase: PHASE2
-
QVA Mechanistic Efficacy Study (Receptor Effects, Etc)
NCT02634983 ·Status: COMPLETED ·Phase: PHASE4
-
Effect of QVA149 on Exercise Tolerance in Patients With Chronic Obstructive Pulmonary Disease (COPD)
NCT01294787 ·Status: COMPLETED ·Phase: PHASE3
-
Efficacy and Safety of NVA237 in Patients With Chronic Obstructive Pulmonary Disease (COPD)
NCT01119950 ·Status: COMPLETED ·Phase: PHASE2
-
A 52-Week, Multicenter, Randomized, Double-Blind, Parallel-Group, Placebo-Controlled Study to Evaluate the Safety and Tolerability of GSK573719/GW642444 and GSK573719 in Subjects With Chronic Obstructive Pulmonary Disease (COPD)
NCT01316887 ·Status: COMPLETED ·Phase: PHASE3
-
Efficacy, Safety and Tolerability of the Co-administration of NVA237 Plus Indacaterol Once Daily Versus Indacaterol Once Daily in Patients With Moderate to Severe Chronic Obstructive Pulmonary Disease (COPD)
NCT01604278 ·Status: COMPLETED ·Phase: PHASE3
-
Efficacy and Safety of Four Doses of Glycopyrronium Bromide (NVA237) in Patients With Stable Chronic Obstructive Pulmonary Disease (COPD), in Comparison to an Active Comparator Tiotropium
NCT00501852 ·Status: COMPLETED ·Phase: PHASE2
-
Effect of NVA237 on Exercise Endurance in Patients With Chronic Obstructive Pulmonary Disease (COPD)
NCT01154127 ·Status: COMPLETED ·Phase: PHASE3
-
Safety and Tolerability of Multiple Inhaled NVA237 Doses in Chronic Obstructive Pulmonary Disease (COPD) Patients
NCT00545311 ·Status: COMPLETED ·Phase: PHASE1
-
A Safety, Tolerability and Efficacy Study With QBW251 in COPD Patients With QBW251
NCT02449018 ·Status: COMPLETED ·Phase: PHASE2
-
Efficacy and Safety of Glycopyrrolate Bromide of COPD Patients
NCT02189577 ·Status: COMPLETED ·Phase: PHASE2