- Trials with a EudraCT protocol (759)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
759 result(s) found for: Respiratory Tract Diseases AND Thoracic Diseases.
Displaying page 7 of 38.
EudraCT Number: 2011-000278-74 | Sponsor Protocol Number: KKL022010 | Start Date*: 2011-07-11 | ||||||||||||||||
Sponsor Name:KRKA, tovarna zdravil, d. d., Novo mesto | ||||||||||||||||||
Full Title: A COMPARATIVE EFFICACY AND SAFETY OF CETYLPYRIDINIUM CHLORIDE 1.0 mg/BENZYDAMINE HYDROCHLORIDE 3 mg FIXED COMBINATION LOZENGES IN SUBJECTS WITH SORE THROAT ASSOCIATED WITH UPPER RESPIRATORY TRACT I... | ||||||||||||||||||
Medical condition: Sore throat associated with upper respiratory infections | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: SI (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2013-004298-28 | Sponsor Protocol Number: MEA117106 | Start Date*: 2014-05-02 | |||||||||||
Sponsor Name:GlaxoSmithKline Research & Development Ltd | |||||||||||||
Full Title: Study MEA117106: Mepolizumab vs. Placebo as add-on treatment for frequently exacerbating COPD patients. | |||||||||||||
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: SE (Completed) CZ (Completed) PL (Completed) IT (Completed) BE (Completed) ES (Completed) EE (Completed) GR (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2011-000762-35 | Sponsor Protocol Number: ID_2882 | Start Date*: 2011-11-18 | |||||||||||
Sponsor Name:A.O. UNIVERSITARIA INTEGRATA DI VERONA | |||||||||||||
Full Title: EFFECTS OF THE VITAMIN D ADMINISTRATION ON RESPIRATORY FUNCTIONS IN PAEDIATRIC PATIENTS SUFFERING FROM EFFORT ASTHMA | |||||||||||||
Medical condition: paediatric patients suffering from effort asthma | |||||||||||||
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Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2020-001026-62 | Sponsor Protocol Number: ETGOL | Start Date*: 2021-10-05 | |||||||||||
Sponsor Name:University Hospital Dr Josep Trueta | |||||||||||||
Full Title: Benefits of inhalation of 7% hypertonic saline solution prior to ELTGOL physiotherapy, in patients with bronchiectasis. A randomized controlled trial. | |||||||||||||
Medical condition: bronchiectasis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2014-002932-15 | Sponsor Protocol Number: 2014-002932-15 | Start Date*: 2014-09-10 | |||||||||||
Sponsor Name:Bispebjerg University Hospital | |||||||||||||
Full Title: The effect of inhaled glucocorticoids on the content of Na+/K+ pumps in human skeletal muscle | |||||||||||||
Medical condition: Asthma | |||||||||||||
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Population Age: Adults | Gender: Male | ||||||||||||
Trial protocol: DK (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2020-004420-42 | Sponsor Protocol Number: COPSACazt | Start Date*: 2022-01-12 | ||||||||||||||||
Sponsor Name:Herlev and Gentofte Hospital, Copenhagen Prospective Studies on Asthma in Childhood (COPSAC) | ||||||||||||||||||
Full Title: Azithromycin for treatment of hospitalized children with asthmatic symptoms - A double-blind, randomized, controlled study | ||||||||||||||||||
Medical condition: Childhood Asthma | ||||||||||||||||||
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Population Age: Infants and toddlers, Children, Under 18 | Gender: Male, Female | |||||||||||||||||
Trial protocol: DK (Trial now transitioned) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2015-004919-20 | Sponsor Protocol Number: StudioLAM | Start Date*: 2016-03-09 | |||||||||||
Sponsor Name:MULTIMEDICA S.P.A. | |||||||||||||
Full Title: A pilot study of nintedanib for lymphangioleiomyomatosis (LAM) | |||||||||||||
Medical condition: Female subjects affected by Llymphangioleiomyomatosis (LAM) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2016-000734-21 | Sponsor Protocol Number: 2014RC07 | Start Date*: 2016-09-07 | |||||||||||
Sponsor Name:University of Dundee & NHS Tayside | |||||||||||||
Full Title: Investigating the mechanism of inhaled corticosteroids associated pneumonia by longitudinal characterisation of the airway microbiome in patients with severe COPD | |||||||||||||
Medical condition: Chronic Obstructive Pulmonary Diseae | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2021-005059-35 | Sponsor Protocol Number: TMP-2204-2021-47 | Start Date*: 2022-01-25 | ||||||||||||||||
Sponsor Name:F4-Pharma GmbH i.G. | ||||||||||||||||||
Full Title: Potential of FX06 to improve disease severity in Acute Respiratory Distress Syndrome patients (Ixion 2.0) | ||||||||||||||||||
Medical condition: Acute Respiratory Distress Syndrome (ARDS) | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: DE (Trial now transitioned) ES (Ongoing) LT (Trial now transitioned) PT (Prematurely Ended) IT (Prematurely Ended) NL (Completed) RO (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: 2020-002069-32 | Sponsor Protocol Number: RPL554-CO-302 | Start Date*: 2020-11-25 | |||||||||||
Sponsor Name:Verona Pharma PLC | |||||||||||||
Full Title: A Phase III Randomized, Double-Blind, Placebo- Controlled Study to Evaluate the Efficacy and Safety of Ensifentrine over 24 Weeks in Patients with Moderate to Severe Chronic Obstructive Pulmonary D... | |||||||||||||
Medical condition: Chronic Obstructive Pulmonary Disease (COPD) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: SK (Completed) BE (Completed) DK (Completed) HU (Completed) BG (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2014-002992-27 | Sponsor Protocol Number: 201496 | Start Date*: 2014-10-10 | |||||||||||
Sponsor Name:GlaxoSmithKline Research & Development Ltd | |||||||||||||
Full Title: 201496: A Study to Evaluate the Efficacy and Safety of 15mg BID Losmapimod (GW856553) Compared to Placebo in Frequently Exacerbating Subjects 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: SK (Prematurely Ended) DE (Completed) BG (Completed) ES (Prematurely Ended) | |||||||||||||
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: 2010-021800-72 | Sponsor Protocol Number: DB2113360 | Start Date*: Information not available in EudraCT | |||||||||||
Sponsor Name:GlaxoSmithKline Research & Development Ltd | |||||||||||||
Full Title: DB2113360: A multicenter trial comparing the efficacy and safety of GSK573719/GW642444 with GW642444 and with tiotropium over 24 weeks in subjects with COPD | |||||||||||||
Medical condition: subjects with COPD | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) PL (Completed) IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2012-003973-24 | Sponsor Protocol Number: ZEP117115 | Start Date*: 2013-01-22 | |||||||||||
Sponsor Name:GlaxoSmithKline Research & Development Limited | |||||||||||||
Full Title: A Multicenter Trial Comparing the Efficacy and Safety of Umeclidinium/Vilanterol 62.5/25 mcg Once Daily with Tiotropium 18 mcg Once Daily over 24 Weeks in Subjects with Chronic Obstructive Pulmonar... | |||||||||||||
Medical condition: Chronic Obstructive Pulmonary Disease (COPD) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: HU (Completed) BG (Completed) ES (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2014-000884-42 | Sponsor Protocol Number: 201316 | Start Date*: 2014-09-12 | |||||||||||
Sponsor Name:GlaxoSmithKline Research & Development Ltd | |||||||||||||
Full Title: A Randomized, Blinded, Double-dummy, Parallel-group Study to Evaluate the Efficacy and Safety of Umeclidinium (UMEC) 62.5 mcg compared with Tiotropium 18 mcg in Subjects with Chronic Obstructive Pu... | |||||||||||||
Medical condition: Chronic Obstructive Pulmonary Disease (COPD) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) IT (Completed) DK (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2012-001585-14 | Sponsor Protocol Number: EPJ-2012 | Start Date*: 2013-01-10 | ||||||||||||||||
Sponsor Name:FISEVI | ||||||||||||||||||
Full Title: Effect of the elimination of colonization by Pneumocystis jirovecii on inflammatory response in patients with chronic obstructive pulmonary disease | ||||||||||||||||||
Medical condition: Chronic obstructive pulmonary disease | ||||||||||||||||||
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Population Age: Adults | Gender: Male, Female | |||||||||||||||||
Trial protocol: ES (Ongoing) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2020-002322-85 | Sponsor Protocol Number: KAN0006 | Start Date*: 2020-07-02 |
Sponsor Name:Kancera AB | ||
Full Title: KAND567 Versus Placebo in Subjects Hospitalized with COVID-19. A Phase II, Randomized, 2-Arm Parallel-Group, Double-blind Study to Evaluate Efficacy, Safety, Tolerability, and Pharmacokinetics. | ||
Medical condition: Acute respiratory distress syndrome (ARDS) in COVID-19 infection | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: SE (Completed) DK (Prematurely Ended) | ||
Trial results: View results |
EudraCT Number: 2014-002305-38 | Sponsor Protocol Number: 2013CV11 | Start Date*: 2015-01-21 | ||||||||||||||||||||||||||
Sponsor Name:University of Dundee/ NHS Tayside | ||||||||||||||||||||||||||||
Full Title: Does allopurinol reduce right ventricular mass in lung disease associated pulmonary hypertension? | ||||||||||||||||||||||||||||
Medical condition: right ventricular hypertrophy associated with COPD or Interstitial Lung Disease and pulmonary hypertension | ||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||
Trial protocol: GB (Completed) | ||||||||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2020-000210-15 | Sponsor Protocol Number: ION-827359-CS2 | Start Date*: 2020-10-08 | |||||||||||
Sponsor Name:Ionis Pharmaceuticals, Inc. | |||||||||||||
Full Title: A Double-Blind, Placebo-Controlled, Phase 2a Study to Assess the Safety, Tolerability, and Efficacy of ION-827359 in Patients with Mild to Moderate COPD with Chronic Bronchitis | |||||||||||||
Medical condition: Mild to Moderate Chronic obstructive pulmonary disease (COPD) with Chronic Bronchitis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) DE (Prematurely Ended) HU (Prematurely Ended) CZ (Prematurely Ended) PL (Prematurely Ended) IT (Prematurely Ended) | |||||||||||||
Trial results: View results |
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