- Trials with a EudraCT protocol (1,479)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (3)
1,479 result(s) found for: Respiratory Disorders.
Displaying page 16 of 74.
| EudraCT Number: 2015-000709-38 | Sponsor Protocol Number: BBR | Start Date*: 2015-10-20 | |||||||||||
| Sponsor Name:Medical University of Graz | |||||||||||||
| Full Title: Acute Effects of Benzbromaron on the pulmonary circulation | |||||||||||||
| Medical condition: Pulmonary arterial hypertension | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: AT (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2007-005045-38 | Sponsor Protocol Number: Colistina | Start Date*: 2007-10-02 | |||||||||||
| Sponsor Name:OSPEDALE POLICLINICO S. MATTEO | |||||||||||||
| Full Title: Pharmacokinetic and colimicine (ColistinaR) concentrations in broncho alveolar lavage in patients affected by pulmonary infections caused by Gram - bacteria. | |||||||||||||
| Medical condition: pulmonary disease caused by Gram - infection | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: IT (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2013-001057-27 | Sponsor Protocol Number: CCD-1207-PR-0091 | Start Date*: 2014-01-24 | |||||||||||
| Sponsor Name:Chiesi Farmaceutici S.p.A. | |||||||||||||
| Full Title: A 52-week, double-blind, randomized, multinational, multicentre, 2-arm parallel-group, active-controlled clinical trial of fixed combination of beclometasone dipropionate plus formoterol fumarate p... | |||||||||||||
| Medical condition: Chronic obstructive pulmonary disease (COPD) | |||||||||||||
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| Population Age: Adults | Gender: Male, Female | ||||||||||||
| Trial protocol: GB (Completed) BE (Completed) HU (Completed) DE (Completed) IT (Completed) CZ (Completed) SK (Completed) PL (Completed) BG (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2020-000697-22 | Sponsor Protocol Number: FGCL-3019-095 | Start Date*: 2020-11-02 | |||||||||||
| Sponsor Name:FibroGen, Inc. | |||||||||||||
| Full Title: Zephyrus II: A Phase 3, Randomized, Double-Blind, Placebo-Controlled Efficacy and Safety Study of Pamrevlumab in Subjects with Idiopathic Pulmonary Fibrosis (IPF). | |||||||||||||
| Medical condition: Idiopathic Pulmonary Fibrosis | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: FR (Prematurely Ended) HU (Prematurely Ended) NL (Prematurely Ended) ES (Prematurely Ended) CZ (Prematurely Ended) DE (Prematurely Ended) DK (Prematurely Ended) IE (Prematurely Ended) PL (Prematurely Ended) IT (Prematurely Ended) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2004-000083-27 | Sponsor Protocol Number: GT-08 | Start Date*: 2004-09-19 |
| Sponsor Name:ALK-Abelló A/S | ||
| Full Title: A randomised, parallel-group, double-blind, placebo-controlled Phase III trial assessing the efficacy and safety of ALK Grass Tablet Phleum pratense in subjects with seasonal grass pollen induced r... | ||
| Medical condition: Rhinoconjunctivitis | ||
| Disease: | ||
| Population Age: Adults | Gender: Male, Female | |
| Trial protocol: SE (Completed) IT (Completed) ES (Completed) AT (Completed) GB (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2016-004318-82 | Sponsor Protocol Number: CTBM100CUS03 | Start Date*: 2017-05-15 | ||||||||||||||||
| Sponsor Name:Novartis Pharmaceuticals Corporation | ||||||||||||||||||
| Full Title: Tobramycin Inhalation Powder (TIP) Administered Once Daily Continuously Versus TIP Administered BID in 28 Day on / 28 Day Off Cycles | ||||||||||||||||||
| Medical condition: Cystic Fibrosis | ||||||||||||||||||
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| Population Age: Children, Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | |||||||||||||||||
| Trial protocol: Outside EU/EEA | ||||||||||||||||||
| Trial results: View results | ||||||||||||||||||
| EudraCT Number: 2011-001581-18 | Sponsor Protocol Number: SCO114520 | Start Date*: 2012-03-29 | |||||||||||
| Sponsor Name:GlaxoSmithKline GmbH & Co. KG | |||||||||||||
| Full Title: Effects of bronchodilatation with salmeterol on the autonomic nervous system | |||||||||||||
| Medical condition: Chronic Obstructive Pulmonary Disease (COPD) | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DE (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2012-002900-42 | Sponsor Protocol Number: D1883C00007 | Start Date*: 2012-08-27 | |||||||||||
| Sponsor Name:AstraZeneca AB | |||||||||||||
| Full Title: A randomised, double-blind placebo- and active-controlled, multi-centre, 6-way cross-over, single-dose phase IIa study to investigate the bronchodilatory and systemic effects of 4 different doses o... | |||||||||||||
| Medical condition: Chronic obstructive pulmonary disease, COPD | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: SE (Prematurely Ended) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2014-003077-42 | Sponsor Protocol Number: CE01-204 | Start Date*: 2015-02-06 | |||||||||||
| Sponsor Name:Imperial College, London | |||||||||||||
| Full Title: A single-centre, double-blind, randomised, placebo-controlled crossover study to evaluate the effect of solithromycin on airway inflammation in male and female patients with chronic obstructive pul... | |||||||||||||
| Medical condition: Chronic Obstructive Pulmonary Disease. | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: GB (Prematurely Ended) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2008-006765-82 | Sponsor Protocol Number: MOXEP | Start Date*: 2009-05-29 | |||||||||||||||||||||
| Sponsor Name:ISTITUTO NAZIONALE DELLE MALATTIE INFETTIVE LAZZARO SPALLANZANI | |||||||||||||||||||||||
| Full Title: Preventive therapy for multidrug-resistant tuberculosis: a multicentre clincal trial. | |||||||||||||||||||||||
| Medical condition: Close contacts of an infectious respiratory of a MDR-TB who are diagnosed with tuberculosis infection that is likely to have been acquired from the MDR-TB case will be eligible for inclusion in th... | |||||||||||||||||||||||
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| Population Age: Adults | Gender: Male, Female | ||||||||||||||||||||||
| Trial protocol: IT (Prematurely Ended) | |||||||||||||||||||||||
| Trial results: (No results available) | |||||||||||||||||||||||
| EudraCT Number: 2011-004936-75 | Sponsor Protocol Number: EVOLUTION | Start Date*: 2012-05-29 | |||||||||||
| Sponsor Name:Cambridge University Hospitals NHS Foundation Trust and University of Cambridge | |||||||||||||
| Full Title: An Evaluation of Losmapimod in patients with Chronic Obstructive Pulmonary Disease (COPD) with systemic inflammation stratified using fibrinogen (EVOLUTION) | |||||||||||||
| Medical condition: The trial team will be looking at patients with Chronic Obstructive Pulmonary Disease and how inflammation affects them. | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: GB (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2012-003791-40 | Sponsor Protocol Number: PSX100201 | Start Date*: 2012-11-26 | |||||||||||
| Sponsor Name:Prosonix Limited | |||||||||||||
| Full Title: An Investigation of the Efficacy, Tolerability and Safety of a Range of Doses of Orally Inhaled Glycopyrronium Bromide (PSX1002-GB pMDI) in Male and Female Patients with Moderate or Severe Chronic ... | |||||||||||||
| Medical condition: Moderate or Severe Chronic Obstructive Pulmonary Disease (COPD) | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: GB (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2011-000429-58 | Sponsor Protocol Number: M/100977/25 | Start Date*: 2011-08-10 | |||||||||||
| Sponsor Name:Almirall S.A. | |||||||||||||
| Full Title: A PHASE IIA, RANDOMISED, SINGLE DOSE, DOUBLE-BLIND, DOUBLE-DUMMY, 6 WAY COMPLETE CROSS-OVER, PLACEBO CONTROLLED CLINICAL TRIAL TO ASSESS THE EFFICACY, SAFETY AND TOLERABILITY OF 4 STRENGTHS OF LAS1... | |||||||||||||
| Medical condition: Stable moderate to severe chronic obstructive pulmonary disease (COPD) | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DE (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2010-020440-35 | Sponsor Protocol Number: D589BC00004 | Start Date*: 2011-09-16 | |||||||||||
| Sponsor Name:Imperial College London | |||||||||||||
| Full Title: GR activity in induced sputum macrophages, and a change in inflammatory biomarkers 2-hours after a single dose of either Symbicort®/Budesonide/Formoterol or placebo in Chronic Obstructive Pulmonary... | |||||||||||||
| Medical condition: Chronic Obstructive Pulmonary Disease (COPD) | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: GB (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2012-000927-42 | Sponsor Protocol Number: HZC116601 | Start Date*: 2012-10-19 | |||||||||||
| Sponsor Name:GlaxoSmithKline Research and Development Ltd | |||||||||||||
| Full Title: A Randomised, Double-Blind, Placebo-Controlled, Cross-Over, Single-Centre Study to Investigate the Acute Lung Deflation Effects of Fluticasone Furoate/Vilanterol Inhalation Powder 100/25mcg Once Da... | |||||||||||||
| Medical condition: Chronic Obstructive Pulmonary Disease (COPD) | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: GB (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2013-001940-71 | Sponsor Protocol Number: BV2013/5 | Start Date*: 2013-12-10 | |||||||||||
| Sponsor Name:OM Pharma SA | |||||||||||||
| Full Title: A Randomized, Placebo Controlled, Double Blinded, Mechanistic trial to investigate the effects of Broncho-Vaxom (OM-85 BV) on the innate immune system in patients with COPD | |||||||||||||
| Medical condition: Chronic Obstructive Pulmonary Disease (COPD) | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: GB (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2010-021802-39 | Sponsor Protocol Number: DB2113374 | Start Date*: Information not available in EudraCT | |||||||||||
| Sponsor Name:GlaxoSmithKline Research & Development Ltd | |||||||||||||
| Full Title: A multicenter trial comparing the efficacy and safety of GSK573719/GW642444 with GSK573719 with tiotropium over 24 weeks in subjects with COPD | |||||||||||||
| Medical condition: Chronic Obstructive Pulmonary Disease (COPD) | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DE (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2010-022895-30 | Sponsor Protocol Number: CCD-1007-PR-0045 | Start Date*: 2011-08-25 | |||||||||||
| Sponsor Name:Chiesi Farmaceutici S.p.A. | |||||||||||||
| Full Title: A 12-week, multicentre, randomised, double-blind, double-dummy, 2-arm parallel group study comparing the efficacy and safety of Foster® 100/6 (beclomethasone dipropionate 100 µg plus formoterol 6 µ... | |||||||||||||
| Medical condition: Male or female patients aged more or equal than 40 years with Chronic Obstructive Pulmonary Disease | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: NL (Prematurely Ended) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2015-001615-13 | Sponsor Protocol Number: 1 | Start Date*: 2015-07-31 | |||||||||||
| Sponsor Name:Imperial College London | |||||||||||||
| Full Title: TARGETING OF THE SMALL AIRWAYS IN PATIENTS WITH COPD: AIRWAY EFFECTS OF TIOTROPIUM -Respimat vs. Handihaler | |||||||||||||
| Medical condition: Chronic Obstructive Pulmonary disease (COPD) | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: GB (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2020-005641-17 | Sponsor Protocol Number: 2019/ABM/01/00074 | Start Date*: 2021-10-12 | |||||||||||
| Sponsor Name:Medical University of Bialystok | |||||||||||||
| Full Title: Non-commercial clinical trial of statins CAncer preventive and Pleiotropic TherApy IN smokers with chronic obstructive pulmonary disease (COPD) Clinical part: Atorvastatin effect on reduction of CO... | |||||||||||||
| Medical condition: Chronic obstructive pulmonary disease (COPD) | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: PL (Trial now transitioned) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
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