deltatrials

Pulmonary disease, chronic obstructive Trials in Marburg, Germany

Conditions / Pulmonary disease, chronic obstructive / Marburg, Germany

Research into Pulmonary disease, chronic obstructive spans multiple therapeutic approaches and trial phases.

19 total trials for this combination

Showing top 10 of 19 trials

Trials

NCT ID Title Status Phase
NCT01313676 Study to Evaluate the Effect of Fluticasone Furoate/Vilanterol on Survival in Subjects With Chronic Obstructive Pulmonary Disease COMPLETED PHASE3
NCT02296138 Comparing the Efficacy of Tiotropium + Olodaterol (5/5 µg) Fixed Dose Combination (FDC) Over Tiotropium 5µg in Reducing Moderate to Severe Exacerbations in Patients With Severe to Very Severe Chronic Obstructive Pulmonary Disease. COMPLETED PHASE3
NCT01126437 Comparison of Tiotropium in the HandiHaler Versus the Respimat in Chronic Obstructive Pulmonary Disease COMPLETED PHASE3
NCT01017952 A Study to Evaluate Annual Rate of Exacerbations and Safety of 3 Dosage Strengths of Fluticasone Furoate (FF)/GW642444 Inhalation Powder in Subjects With Chronic Obstructive Pulmonary Disease (COPD) COMPLETED PHASE3
NCT00528996 An Efficacy and Safety Study to Compare Three Doses of BEA 2180 BR to Tiotropium and Placebo in the Respimat Inhaler. COMPLETED PHASE2
NCT04072887 Dose-range Finding Efficacy and Safety Study for QBW251 in COPD Patients COMPLETED PHASE2
NCT02164513 A Study Comparing the Efficacy, Safety and Tolerability of Fixed Dose Combination (FDC) of FF/UMEC/VI With the FDC of FF/VI and UMEC/VI; Administered Once-daily Via a Dry Powder Inhaler (DPI) in Subjects With Chronic Obstructive Pulmonary Disease (COPD) COMPLETED PHASE3
NCT00975195 Inhaled Corticosteroid Withdrawal in Patients With Chronic Obstructive Pulmonary Disease COMPLETED PHASE4
NCT03034915 A 24-week Study to Compare Umeclidinium/Vilanterol (UMEC/VI), UMEC and Salmeterol in Subjects With Chronic Obstructive Pulmonary Disease (COPD) COMPLETED PHASE4
NCT00563381 Tiotropium Once Daily 18 Mcg Versus Salmeterol Twice Daily 50 Mcg on Time to First Exacerbation in COPD Patients. COMPLETED PHASE4

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