- Trials with a EudraCT protocol (524)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
524 result(s) found for: Respiratory Tract Diseases AND Asthma.
Displaying page 1 of 27.
EudraCT Number: 2015-002555-10 | Sponsor Protocol Number: ORCA2015 | Start Date*: 2015-11-19 | ||||||||||||||||||||||||||||||||||||
Sponsor Name:Imperial College | ||||||||||||||||||||||||||||||||||||||
Full Title: Effect of the CRTH2 antagonist OC459 on the response to rhinovirus challenge in asthma | ||||||||||||||||||||||||||||||||||||||
Medical condition: Asthma | ||||||||||||||||||||||||||||||||||||||
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Population Age: Adults | Gender: Male, Female | |||||||||||||||||||||||||||||||||||||
Trial protocol: GB (Completed) | ||||||||||||||||||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2020-000883-42 | Sponsor Protocol Number: APHP180614 | Start Date*: 2021-01-18 | |||||||||||
Sponsor Name:ASSISTANCE PUBLIQUE - HOPITAUX DE PARIS | |||||||||||||
Full Title: Impact of omalizumab withdrawal after a 3 year duration treatment in well controlled severe allergic asthma : a multicentric randomized controlled trial | |||||||||||||
Medical condition: well controlled severe allergic asthma | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2011-002816-97 | Sponsor Protocol Number: ADC3680-04 | Start Date*: 2011-09-22 | |||||||||||
Sponsor Name:Pulmagen Therapeutics LLP | |||||||||||||
Full Title: A Randomised, Placebo-Controlled, Double-Blind, Parallel Group Phase II Study to Assess the Safety, Tolerability and Pharmacokinetics of ADC3680B in Subjects with Partly Controlled Atopic Asthma | |||||||||||||
Medical condition: Asthma | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
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: 2016-002276-27 | Sponsor Protocol Number: PVSD-ICS | Start Date*: 2016-08-04 | |||||||||||
Sponsor Name:Medisch Spectrum Twente | |||||||||||||
Full Title: The predictive value of the acute effect of beclomethasone-dipropionate on a mannitol challenge test for the outcome of longterm treatment with beclomethasone-dipropionate in childhood asthma | |||||||||||||
Medical condition: exercise induced bronchoconstriction asthma | |||||||||||||
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Population Age: Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2014-002151-26 | Sponsor Protocol Number: Z7200K02 | Start Date*: 2014-08-27 | ||||||||||||||||||||||||||
Sponsor Name:Zambon Spa | ||||||||||||||||||||||||||||
Full Title: A Double Blind, Double Dummy, Randomized, Two Way Cross-Over Study To Compare The Effects Of Z7200 And Symbicort® Turbohaler On Functional Respiratory Imaging Parameters In Asthmatic Patients | ||||||||||||||||||||||||||||
Medical condition: Asthma | ||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||
Trial protocol: BE (Completed) | ||||||||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2012-005789-36 | Sponsor Protocol Number: FLUI-2012-94 | Start Date*: 2013-03-04 | ||||||||||||||||||||||||||
Sponsor Name:FluidDA nv | ||||||||||||||||||||||||||||
Full Title: Double blind, double dummy, randomized, two way cross-over study to compare the effects of Seretide® Evohaler (supplied by Allen & Hanburys, UK) and a generic test HFA pMDI (manufactured by Cipla L... | ||||||||||||||||||||||||||||
Medical condition: Asthma | ||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||
Trial protocol: BE (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: 2020-002977-84 | Sponsor Protocol Number: BECRO/RESP/ANASSA-PD | Start Date*: 2020-10-16 | ||||||||||||||||
Sponsor Name:RESPIRENT Pharmaceuticals | ||||||||||||||||||
Full Title: A phase III, randomized, multicenter, parallel-group clinical trial for examining the therapeutic equivalence between Fluticasone propionate 100 mcg/blister oral inhalation powder/Respirent Pharmac... | ||||||||||||||||||
Medical condition: Asthma is a heterogeneous disease, usually characterized by chronic airway inflammation. It is defined by the history of respiratory symptoms such as wheeze, shortness of breath, chest tightness an... | ||||||||||||||||||
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Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: GR (Completed) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2017-000702-38 | Sponsor Protocol Number: D3250C00036 | Start Date*: 2017-07-06 | |||||||||||
Sponsor Name:AstraZeneca AB | |||||||||||||
Full Title: A Multicentre, Randomised, Double-blind, Parallel Group, Placebocontrolled, Phase 3 Efficacy and Safety Study of Benralizumab (MEDI-563) Added to Medium to High-dose Inhaled Corticosteroid Plus Lon... | |||||||||||||
Medical condition: Asthma | |||||||||||||
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Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: Outside EU/EEA | |||||||||||||
Trial results: View results |
EudraCT Number: 2009-011975-60 | Sponsor Protocol Number: AC-060A202 | Start Date*: 2010-09-30 | |||||||||||
Sponsor Name:Actelion Pharmaceuticals Ltd. | |||||||||||||
Full Title: A multi-center, double-blind, placebo-controlled, parallel-group study to establish proof-of-concept and explore the efficacy of different doses of ACT-129968 in adult patients with partly contro... | |||||||||||||
Medical condition: Allergic asthma | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: SE (Completed) DE (Completed) HU (Completed) PL (Completed) BG (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2013-000737-12 | Sponsor Protocol Number: LPI-1201 | Start Date*: 2013-09-09 | |||||||||||
Sponsor Name:Lallemand Pharma International AG | |||||||||||||
Full Title: The Influence of Polyvalent Mechanical Bacterial Lysate (ISMIGEN®) on Clinical Course of Asthma and Related Immunological parameters in Asthmatic Children (EOLIA Study): Randomized, Double Blind, P... | |||||||||||||
Medical condition: IgE-dependent asthma (diagnosis of asthma according to the GINA definition) in a paediatric population (6 thru 16 years old) | |||||||||||||
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Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: PL (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2012-000039-22 | Sponsor Protocol Number: CCD-1113-PR-0074 | Start Date*: 2012-06-05 | |||||||||||
Sponsor Name:CHIESI | |||||||||||||
Full Title: AN OPEN LABEL PLACEBO STUDY TO ASSESS THE INHALATION PROFILE OBTAINED BY ACOUSTIC MONITORING IN ASTHMATIC PATIENTS USING THE NEXTHALER DRY POWDER INHALER (DPI) DEVICE. | |||||||||||||
Medical condition: Adults asthmatics Patients with varying degrees of disease control. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2015-001572-22 | Sponsor Protocol Number: PDY14192 | Start Date*: 2015-12-01 | |||||||||||
Sponsor Name:SANOFI-AVENTIS RECHERCHE ET DEVELOPPEMENT | |||||||||||||
Full Title: An exploratory, randomized, double-blind, placebo-controlled study of the effects of dupilumab on airway inflammation of adults with persistent asthma | |||||||||||||
Medical condition: Asthma | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) GB (Completed) SE (Completed) DK (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2013-003856-19 | Sponsor Protocol Number: LTS12551 | Start Date*: 2014-05-28 | |||||||||||
Sponsor Name:Sanofi-aventis recherche et développement | |||||||||||||
Full Title: Open label extension study to evaluate the long-term safety and tolerability of dupilumab in patients with asthma who participated in previous dupilumab asthma clinical study | |||||||||||||
Medical condition: Asthma | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Completed) IT (Completed) PL (Completed) DE (Completed) GB (Completed) NL (Completed) HU (Completed) BE (Completed) DK (Completed) SE (Completed) Outside EU/EEA | |||||||||||||
Trial results: View results |
EudraCT Number: 2006-002791-18 | Sponsor Protocol Number: 0476-302 | Start Date*: 2006-09-28 | |||||||||||
Sponsor Name:Suomen MSD Oy | |||||||||||||
Full Title: A Multicenter, Randomized, Double-Blind, Double-Dummy, Parallel-Group Study Evaluating the Effects of 2 Different Regimens of Montelukast (Daily Dosing and Intermittent, Episode-Driven Dosing) Comp... | |||||||||||||
Medical condition: episodic or intermittent asthma | |||||||||||||
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Population Age: Children, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: FI (Completed) DK (Completed) DE (Completed) IT (Completed) LT (Completed) FR (Completed) Outside EU/EEA | |||||||||||||
Trial results: View results |
EudraCT Number: 2017-002134-23 | Sponsor Protocol Number: LPS15023 | Start Date*: 2018-11-19 | |||||||||||
Sponsor Name:sanofi-aventis groupe | |||||||||||||
Full Title: Open-label, Interventional, Cohort Study to Evaluate Long-term Safety of Dupilumab in Patients with Moderate to Severe Asthma who Completed the TRAVERSE-LTS12551Clinical Trial | |||||||||||||
Medical condition: Asthma | |||||||||||||
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Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Completed) BE (Completed) DE (Completed) NL (Completed) Outside EU/EEA | |||||||||||||
Trial results: View results |
EudraCT Number: 2014-002705-38 | Sponsor Protocol Number: 3103013 | Start Date*: 2014-11-18 | ||||||||||||||||
Sponsor Name:Orion Corporation Orion Pharma | ||||||||||||||||||
Full Title: STUDY COMPARING BRONCHODILATOR EFFICACY OF TWO DRY POWDER INHALERS, BUDESONIDE/FORMOTEROL EASYHALER AND SYMBICORT TURBUHALER; A RANDOMISED, DOUBLE-BLIND, DOUBLE-DUMMY, MULTICENTRE, SINGLE DOSE, CRO... | ||||||||||||||||||
Medical condition: Asthma | ||||||||||||||||||
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Population Age: Adults | Gender: Male, Female | |||||||||||||||||
Trial protocol: HU (Completed) BG (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2021-006681-21 | Sponsor Protocol Number: FVGEXACT@home2021 | Start Date*: 2022-11-17 | |||||||||||
Sponsor Name:Franciscus Gasthuis & Vlietland | |||||||||||||
Full Title: Expertise Asthma COPD Program with Digital Support | |||||||||||||
Medical condition: Asthma | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2022-003466-20 | Sponsor Protocol Number: ARORAGE-1001 | Start Date*: 2023-06-01 | |||||||||||
Sponsor Name:Arrowhead Pharmaceuticals, Inc. | |||||||||||||
Full Title: A Phase 1/2a Study Evaluating the Effects of ARO-RAGE in Healthy Subjects and Patients with Asthma | |||||||||||||
Medical condition: Asthma | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Ongoing) PL (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
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