- Trials with a EudraCT protocol (688)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (5)
688 result(s) found for: COPD.
Displaying page 1 of 35.
EudraCT Number: 2019-001800-39 | Sponsor Protocol Number: D3251C00014 | Start Date*: 2019-11-14 | |||||||||||
Sponsor Name:AstraZeneca AB | |||||||||||||
Full Title: A Multicenter, Randomized, Double-blind, Chronic-dosing, Parallel-group, Placebo-controlled Phase 3 Study to Evaluate the Efficacy and Safety of Benralizumab 100 mg in Patients with Moderate to V... | |||||||||||||
Medical condition: Chronic Obstructive Pulmonary Disease | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Trial now transitioned) PL (Trial now transitioned) HU (Trial now transitioned) CZ (Trial now transitioned) DE (Trial now transitioned) AT (Trial now transitioned) ES (Ongoing) GB (GB - no longer in EU/EEA) NL (Ongoing) BE (Trial now transitioned) GR (Trial now transitioned) IT (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2021-003797-30 | Sponsor Protocol Number: D9180C00003 | Start Date*: 2022-01-31 | |||||||||||
Sponsor Name:AstraZeneca AB | |||||||||||||
Full Title: A Phase III, Multicentre, Randomized, Double-blind, Chronic-dosing, Parallel-group, Placebo-controlled Study to Evaluate the Efficacy and Safety of Two Dose Regimens of Tozorakimab in Participants ... | |||||||||||||
Medical condition: Chronic Obstructive Pulmonary Disease (COPD) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: NO (Trial now transitioned) FI (Trial now transitioned) DK (Trial now transitioned) SE (Trial now transitioned) NL (Trial now transitioned) ES (Ongoing) HU (Trial now transitioned) CZ (Trial now transitioned) BG (Trial now transitioned) PT (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2006-002933-18 | Sponsor Protocol Number: COPDIT | Start Date*: 2007-11-05 | |||||||||||
Sponsor Name:InfectoPharm Arzneimittel und Consilium GmbH | |||||||||||||
Full Title: Multizentrische, randomisierte, doppelblinde, placebokontrollierte Phase III-Studie zur (Langzeit-) Add On-Behandlung der COPD (Schweregrad III/IV) mit 2 x 80 mg inhalativem Tobramycin (Gernebcin) | |||||||||||||
Medical condition: Austherapierte schwere bis sehr schwere COPD (Schweregrad III-IV) mit mindestens 2 COPD-Exazerbations-bedingten Hospitalisationen innerhalb der letzten 12 Monate | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2010-019685-87 | Sponsor Protocol Number: RO-2455-404-RD | Start Date*: 2011-04-27 | |||||||||||
Sponsor Name:Takeda Pharma A/S | |||||||||||||
Full Title: Effect of roflumilast on exacerbation rate in patients with COPD treated with fixed combinations of LABA and ICS. A 52-week, randomised double-blind trial with roflumilast 500 μg versus placebo | |||||||||||||
Medical condition: severe chronic obstructive pulmonary disease (COPD) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) BE (Completed) DE (Completed) AT (Completed) DK (Completed) GR (Completed) NL (Completed) HU (Completed) SK (Completed) IT (Completed) ES (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2017-004369-29 | Sponsor Protocol Number: 206854 | Start Date*: 2018-04-24 | |||||||||||
Sponsor Name:GlaxoSmithKline Research & Development Limited | |||||||||||||
Full Title: The Clinical Effectiveness of Fluticasone Furoate/Umeclidinium Bromide/Vilanterol in a Single Inhaler (TRELEGYTM ELLIPTATM) when Compared with Non-ELLIPTA Multiple Inhaler Triple Therapies in COPD ... | |||||||||||||
Medical condition: Chronic Obstructive Pulmonary Disease (COPD) which may be called emphysema or chronic bronchitis. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: SE (Completed) GB (Completed) NL (Completed) ES (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2012-003253-28 | Sponsor Protocol Number: MV130-SLG-001 | Start Date*: 2012-12-13 | |||||||||||
Sponsor Name:Inmunotek S.L. | |||||||||||||
Full Title: Randomized double-blind placebo-controlled prospective, parallel, multicentre clinical trial of bacterial polivalent vaccine (BACTEK ®)administered by sublingual mucosa in subjects with chronic o... | |||||||||||||
Medical condition: Chronic obstructive pulmonary disease (COPD) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Ongoing) | |||||||||||||
Trial results: View results |
EudraCT Number: 2014-001053-16 | Sponsor Protocol Number: D2550C00005 | Start Date*: 2014-10-07 | |||||||||||
Sponsor Name:AstraZeneca AB | |||||||||||||
Full Title: A 12-week Phase IIa, Double-blind, Placebo-controlled, Randomized Study to Investigate the Efficacy and Safety of AZD7624 in COPD Patients with a History of Frequent Acute Exacerbations while on Ma... | |||||||||||||
Medical condition: Chronic Obstructive Pulmonary Disease (COPD) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2005-003937-42 | Sponsor Protocol Number: BY217/M2-124 | Start Date*: 2005-06-16 | |||||||||||
Sponsor Name:ALTANA Pharma AG | |||||||||||||
Full Title: Effect of roflumilast on exacerbation rate in patients with COPD A 52 weeks, 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) HU (Completed) GB (Completed) DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2012-004966-16 | Sponsor Protocol Number: CQVA149A2318 | Start Date*: 2013-02-27 | |||||||||||
Sponsor Name:Novartis Pharma AG | |||||||||||||
Full Title: A 52-week treatment, multi-center, randomized, double-blind, double-dummy, parallel-group, active controlled study to compare the effect of QVA149 (indacaterol maleate / glycopyrronium bromide) wit... | |||||||||||||
Medical condition: subjects with moderate to very severe COPD | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: SK (Completed) HU (Completed) SE (Completed) ES (Completed) AT (Completed) LT (Completed) NL (Completed) CZ (Completed) FI (Completed) DE (Completed) BE (Completed) IS (Completed) IT (Completed) PT (Completed) NO (Completed) PL (Completed) EE (Completed) DK (Completed) BG (Completed) LV (Completed) GR (Completed) GB (Completed) LU (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2019-001363-67 | Sponsor Protocol Number: D5241C00001 | Start Date*: 2019-10-22 | |||||||||||
Sponsor Name:AstraZeneca AB | |||||||||||||
Full Title: A Randomized, Double-blind, Placebo-controlled, Parallel Group, Multicenter, Phase 2a Study to Explore the Efficacy and Safety of Tezepelumab in Patients with Moderate to Very Severe Chronic Obstru... | |||||||||||||
Medical condition: Moderate to Very Severe Chronic Obstructive Pulmonary Disease (COPD) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Completed) NL (Completed) FR (Completed) DE (Completed) ES (Ongoing) GB (GB - no longer in EU/EEA) | |||||||||||||
Trial results: View results |
EudraCT Number: 2009-010084-16 | Sponsor Protocol Number: 6645 | Start Date*: 2009-07-24 | |||||||||||
Sponsor Name:Barts Health NHS Trust | |||||||||||||
Full Title: Randomised, Multi-Centre, Double-Blind, Placebo-Controlled Trial of Vitamin D Supplementation in Patients with 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) | |||||||||||||
Trial results: View results |
EudraCT Number: 2011-004166-16 | Sponsor Protocol Number: SimvaCOPD | Start Date*: 2012-08-07 | ||||||||||||||||
Sponsor Name:Abteilung für Pulmologie, Landesklinikum Thermenregion Hochegg | ||||||||||||||||||
Full Title: Does simvastatin treatment affect COPD exacerbations? - Evaluation in a randomized controlled trial | ||||||||||||||||||
Medical condition: patients with COPD in stage II-IV (according to the GOLD classification) | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: AT (Completed) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2019-004178-24 | Sponsor Protocol Number: 1704 | Start Date*: 2020-06-13 | ||||||||||||||||
Sponsor Name:Amphia | ||||||||||||||||||
Full Title: Defining long-term macrolide maintenance therapy in COPD: a single center randomized controlled trial: | ||||||||||||||||||
Medical condition: Chronic obstructive pulmonary disease COPD | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: NL (Ongoing) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2012-002952-17 | Sponsor Protocol Number: COPDIron | Start Date*: 2012-11-12 |
Sponsor Name:University of Oxford | ||
Full Title: Effects of intravenous iron on hypoxic pulmonary responses in COPD | ||
Medical condition: Chronic Obstructive Pulmonary Disease (COPD) | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (Completed) | ||
Trial results: View results |
EudraCT Number: 2013-004297-98 | Sponsor Protocol Number: 117113 | Start Date*: 2014-09-01 | |||||||||||
Sponsor Name:GlaxoSmithKline Research & Development Ltd | |||||||||||||
Full Title: Study 117113: Mepolizumab vs. Placebo as add-on treatment for frequently exacerbating COPD patients characterized by eosinophil level. | |||||||||||||
Medical condition: Treatment of severe Chronic Obstructive Pulmonary Disease (COPD) in patients presenting frequent exacerbations | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Completed) SK (Completed) DE (Completed) GB (Completed) DK (Completed) RO (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2018-004267-32 | Sponsor Protocol Number: CQAW039E12201 | Start Date*: 2019-04-10 | |||||||||||
Sponsor Name:Novartis Pharma AG | |||||||||||||
Full Title: A multi-center, proof-of-mechanism study of multiple, oral doses of fevipiprant (QAW039) in COPD patients with eosinophilia | |||||||||||||
Medical condition: Chronic obstructive pulmonary disease with eosinophilia | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Prematurely Ended) BE (Prematurely Ended) DE (Prematurely Ended) ES (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2013-003510-41 | Sponsor Protocol Number: 200163 | Start Date*: 2014-01-24 | |||||||||||
Sponsor Name:GlaxoSmithKline Research & Development Ltd | |||||||||||||
Full Title: A two part, Phase IIa, randomized, placebo-controlled study to investigate the safety, tolerability, pharmacokinetics, pharmacodynamics, and clinical efficacy of oral danirixin (GSK1325756) in symp... | |||||||||||||
Medical condition: Chronic Obstructive Pulmonary Disease | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2011-005389-39 | Sponsor Protocol Number: D2340C00011 | Start Date*: 2012-03-12 | |||||||||||
Sponsor Name:ASTRAZENECA | |||||||||||||
Full Title: A phase-II, double-blind, placebo-controlled, randomised, parallelgroup, multi-centre study to assess the efficacy and safety of two staggered dose levels of inhaled once daily AZD5423 or twice d... | |||||||||||||
Medical condition: Chronic obstructive pulmonary disease | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) SK (Completed) BG (Completed) HU (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2009-013256-69 | Sponsor Protocol Number: CQVA149A2304 | Start Date*: 2010-04-13 | ||||||||||||||||
Sponsor Name:Novartis Pharma Services AG | ||||||||||||||||||
Full Title: A 64-week treatment, multi-center, randomized, double-blind, parallel-group, active controlled study to evaluate the effect of QVA149 (110/50 μg o.d.) vs NVA237 (50 μg o.d.) and open-label tiotropi... | ||||||||||||||||||
Medical condition: Chronic Obstructive Pulmonary Disease (COPD) | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: DE (Completed) HU (Completed) FI (Completed) CZ (Completed) NL (Completed) SK (Completed) ES (Completed) GB (Completed) DK (Completed) FR (Completed) EE (Completed) IE (Completed) IT (Completed) PL (Completed) AT (Completed) GR (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2016-000155-28 | Sponsor Protocol Number: PT009003 | Start Date*: 2016-11-21 | |||||||||||
Sponsor Name:Pearl Therapeutics, Inc. (Pearl) | |||||||||||||
Full Title: A Randomized, Double-Blind, Parallel Group, Multi-Center Study to Assess the Efficacy and Safety of PT009 compared to PT005 in Subjects With Moderate to Very Severe COPD | |||||||||||||
Medical condition: Moderate to Very Severe Chronic Obstructive Pulmonary Disease (COPD) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Completed) BE (Completed) GB (Completed) DE (Completed) ES (Completed) AT (Completed) IT (Completed) | |||||||||||||
Trial results: View results |
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