- Trials with a EudraCT protocol (652)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (5)
652 result(s) found for: Chronic Obstructive Pulmonary Disease.
Displaying page 1 of 33.
EudraCT Number: 2006-004610-41 | Sponsor Protocol Number: 205.368 | Start Date*: 2007-05-28 | |||||||||||
Sponsor Name:Boehringer Ingelheim España, S. A. | |||||||||||||
Full Title: Ensayo aleatorizado, doble ciego, controlado con placebo de dos años de duración para evaluar cambios en la tolerancia al ejercicio en pacientes con EPOC tratados con Tiotropio (Spiriva® HandiHaler... | |||||||||||||
Medical condition: Enfermedad Pulmonar Obstructiva Crónica (EPOC) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Completed) DE (Completed) PT (Completed) IT (Completed) AT (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2006-001954-28 | Sponsor Protocol Number: CQAB149B2334 | Start Date*: 2006-10-10 | |||||||||||
Sponsor Name:NovartisPharma Services AG | |||||||||||||
Full Title: A 52-week treatment, multicenter, randomized, double-blind, double dummy, placebo-controlled, parallel-group study to assess the efficacy, safety and tolerability of indacaterol (300 & 600 µg o.d.)... | |||||||||||||
Medical condition: Chronic Obstructive Pulmonary Disease (COPD) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Completed) BE (Completed) DK (Completed) HU (Completed) GB (Completed) SK (Completed) DE (Completed) CZ (Completed) EE (Completed) LT (Completed) SE (Completed) LV (Completed) IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2008-002151-25 | Sponsor Protocol Number: D4260C00007 | Start Date*: 2008-07-03 | |||||||||||
Sponsor Name:AstraZeneca AB | |||||||||||||
Full Title: A Double-Blind, Randomised, Placebo-Controlled, Parallel Group Multi-Centre Phase IIa Study to Assess the Effects on Biomarkers in Induced Sputum, Blood and Urine of AZD1236 Administered as Oral Ta... | |||||||||||||
Medical condition: Chronic Obstructive Pulmonary Disease (study conducted in men or women, not of child bearing potential, aged 40 years or above). | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Completed) FI (Completed) DK (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2004-000025-29 | Sponsor Protocol Number: CQAB149B2205 | Start Date*: 2004-08-10 | |||||||||||
Sponsor Name:Novartis Sweden AB | |||||||||||||
Full Title: Full title of the trial : A randomized, double-blind, placebo-controlled, parallel group, multi-center, multiple dose (7 days) dose-ranging study, to assess the efficacy and safety of 4 doses of ... | |||||||||||||
Medical condition: Moderate to severe Chronic Obstructive Pulmonary Disease | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: SE (Completed) DK (Completed) BE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2008-002237-73 | Sponsor Protocol Number: KOL-PH-SILD2008 | Start Date*: 2008-07-03 | ||||||||||||||||
Sponsor Name:Dept. of Pharmacology, Aarhus University | ||||||||||||||||||
Full Title: Sildenafil Treatment of COPD associated Pulmonary Hypertension | ||||||||||||||||||
Medical condition: Pulmonary hypertension in patients with chronic obstructive lung disease (COPD) | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: DK (Prematurely Ended) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2009-014418-86 | Sponsor Protocol Number: 1222.40 | Start Date*: 2010-01-05 | |||||||||||
Sponsor Name:Boehringer Ingelheim bv | |||||||||||||
Full Title: Randomised, double-blind, double-dummy, placebo-controlled, 4-way cross-over study to characterise the 24-hour FEV1-time profiles of BI 1744 CL 5µg and 10µg (oral inhalation, delivered by the Respi... | |||||||||||||
Medical condition: Chronic Obstructive Pulmonary Disease (COPD) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Completed) DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2011-002563-23 | Sponsor Protocol Number: CD-RI-MEDI8968-1103 | Start Date*: 2012-03-15 | |||||||||||
Sponsor Name:MedImmune Limited | |||||||||||||
Full Title: A Phase 2 Double-blind, Placebo-controlled Study to Evaluate the Efficacy of MEDI8968 in Chronic Obstructive Pulmonary Disease | |||||||||||||
Medical condition: Chronic Obstructive Pulmonary Disease | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) HU (Completed) LV (Completed) CZ (Completed) LT (Completed) PL (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2004-004442-40 | Sponsor Protocol Number: BY217/M2-114 | Start Date*: 2005-03-21 | |||||||||||
Sponsor Name:ALTANA Pharma AG | |||||||||||||
Full Title: 500µg roflumilast once daily in combination with 50µg salmeterol twice daily versus 50µg salmeterol twice daily alone over 52 weeks in patients with COPD. | |||||||||||||
Medical condition: COPD | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: AT (Completed) GB (Completed) ES (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2010-021217-23 | Sponsor Protocol Number: D3550C00002 | Start Date*: 2010-10-22 | |||||||||||
Sponsor Name:AstraZeneca AB | |||||||||||||
Full Title: A 4 Week, Double Blind, Placebo Controlled, Randomised, Parallel Group, Multicentre, Phase IIa Study to Investigate the Safety and Tolerability of AZD5069 as Oral Capsules in Patients with Moderate... | |||||||||||||
Medical condition: COPD | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) HU (Completed) BG (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2006-004508-37 | Sponsor Protocol Number: BY217/M2-128 | Start Date*: 2007-01-08 | |||||||||||
Sponsor Name:Nycomed GmbH | |||||||||||||
Full Title: Effect of roflumilast in COPD patients treated with tiotropium. A 24-week, double-blind study with 500 µg roflumilast once daily versus placebo. | |||||||||||||
Medical condition: Chronic obstructive pulmonary disease (COPD) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) GB (Completed) HU (Completed) AT (Completed) IT (Completed) ES (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2009-010665-23 | Sponsor Protocol Number: CQAB149B2350 | Start Date*: 2009-07-01 | |||||||||||
Sponsor Name:Novartis Pharma Services AG | |||||||||||||
Full Title: A 12-week treatment, multi-center, randomized, parallel group, blinded, double dummy study to compare the efficacy and safety of Indacaterol (150 μg o.d.) delivered via a SDDPI with Tiotropium (18 ... | |||||||||||||
Medical condition: COPD (chronic obstructive pulmonary disease) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) FI (Completed) ES (Completed) AT (Completed) FR (Completed) HU (Completed) DK (Completed) PL (Completed) GB (Completed) SK (Completed) BE (Completed) IT (Completed) GR (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2007-003655-36 | Sponsor Protocol Number: CQVA149A2204 | Start Date*: 2008-02-29 | |||||||||||
Sponsor Name:Novartis Pharma Services AG | |||||||||||||
Full Title: A randomized, double-blind, placebo controlled, multicentre study to determine the effect of QVA149 on lung function in patients with Chronic Obstructive Pulmonary Disease (COPD) | |||||||||||||
Medical condition: Chronic Obstructive Pulmonary Disease | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) NL (Completed) BE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2005-005080-28 | Sponsor Protocol Number: BY217/M2-127 | Start Date*: 2006-04-04 | |||||||||||
Sponsor Name:ALTANA Pharma AG | |||||||||||||
Full Title: Effect of roflumilast in COPD patients treated with salmeterol. A 24 week, double blind study with 500 mcg roflumilast once daily versus placebo | |||||||||||||
Medical condition: Chronic obstructive pulmonary disease (COPD) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: AT (Completed) DE (Completed) GB (Completed) ES (Completed) BE (Completed) IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2009-010864-40 | Sponsor Protocol Number: D1882C00003 | Start Date*: 2009-06-18 | |||||||||||
Sponsor Name:AstraZeneca AB | |||||||||||||
Full Title: A double-blind, double-dummy, placebo-controlled, randomised, multi-centre, 5-way cross-over, single-dose study to investigate the local and systemic effects of inhaled AZD9164 compared to tiotropi... | |||||||||||||
Medical condition: Chronic Obstructive Pulmonary Disease (COPD) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: SE (Completed) DK (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2009-013504-32 | Sponsor Protocol Number: CNVA237A2304 | Start Date*: 2009-10-20 | ||||||||||||||||
Sponsor Name:Novartis Farmaceutica, S.A. | ||||||||||||||||||
Full Title: Estudio aleatorizado, doble ciego, de grupos paralelos, controlado con placebo para valorar la eficacia, seguridad y tolerabilidad durante un tratamiento de 26 semanas con NVA237 en pacientes con ... | ||||||||||||||||||
Medical condition: Enfermedad Pulmonar Obstructiva Crónica (EPOC) | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: ES (Completed) NL (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2008-006305-16 | Sponsor Protocol Number: CPJMR0052203 | Start Date*: 2009-01-30 | |||||||||||
Sponsor Name:Novartis Pharma Services AG | |||||||||||||
Full Title: A randomized, open-label, multicenter, two-period crossover study to evaluate the 24 hour bronchodilator profile of Tiotropium Bromide Respimat® administered once daily versus twice daily in patien... | |||||||||||||
Medical condition: Chronic Obstructive Pulmonary Disease (COPD) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) FR (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2006-003184-31 | Sponsor Protocol Number: Hx-CD20-408 | Start Date*: 2007-05-31 | |||||||||||
Sponsor Name:Genmab A/S | |||||||||||||
Full Title: A double-blind, randomized, placebo-controlled, multi-center, Clinical Trial of ofatumumab, a fully human monoclonal anti-CD20 antibody in patients with moderate to severe stage Chronic Obstructive... | |||||||||||||
Medical condition: Moderate to severe stage of Chronic Obstructive Pulmonary Disease (COPD) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Prematurely Ended) DK (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2006-003634-15 | Sponsor Protocol Number: CQAB149B2211 | Start Date*: 2006-09-13 | |||||||||||
Sponsor Name:NovartisPharma Services AG | |||||||||||||
Full Title: An exploratory, double-blind comparison of inspiratory capacity (IC) and FEV1 in COPD patients following single dose administration of indacaterol and placebo and open-label b.i.d. administration o... | |||||||||||||
Medical condition: Mild to severe COPD | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Completed) DE (Completed) GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2011-002018-35 | Sponsor Protocol Number: ARC209/A | Start Date*: 2013-03-08 | ||||||||||||||||
Sponsor Name:ASSOCIAZIONE ITALIANA PNEUMOLOGI OSPEDALIERI | ||||||||||||||||||
Full Title: SPHERIC-1OE (Sildenafil and Pulmonary HypERtension In COPD – Open Extension) - A multicenter, longitudinal, 12 months open-label study, for the observation of the use of sildenafil in the treatment... | ||||||||||||||||||
Medical condition: Patients with pulmonary hypertension associated with chronic obstructive pulmonary disease enrolled in the study SPHERIC-1 | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: IT (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2010-018763-42 | Sponsor Protocol Number: 2008CV17 | Start Date*: 2010-07-14 | ||||||||||||||||
Sponsor Name:University of Dundee | ||||||||||||||||||
Full Title: Do Phosphodiesterase 5 Inhibitors Improve Exercise Capacity in COPD Patients with Pulmonary Hypertension? | ||||||||||||||||||
Medical condition: Chronic obstructive pulmonary disease Pulmonary hypertension (secondary to chronic obstructive pulmonary disease) | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: GB (Completed) | ||||||||||||||||||
Trial results: View results |
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