- Trials with a EudraCT protocol (354)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
354 result(s) found for: Allergic Asthma.
Displaying page 2 of 18.
EudraCT Number: 2013-001103-36 | Sponsor Protocol Number: 2013RC01 | Start Date*: 2013-05-27 | |||||||||||
Sponsor Name:Tayside Medical Sciences Centre on behalf of University of Dundee & NHS Tayside | |||||||||||||
Full Title: Randomised controlled single and chronic dosing crossover comparison of extra fine particle formoterol and coarse particle salmeterol in asthmatic patients with persistent small airways dysfunction | |||||||||||||
Medical condition: Asthma | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2008-007244-33 | Sponsor Protocol Number: LPA112046 | Start Date*: 2009-04-08 | |||||||||||
Sponsor Name:GlaxoSmithKline Research & Development Limited | |||||||||||||
Full Title: The efficacy of orally administered GSK2190915 as an add-on to current therapy in subjects with moderate to severe asthma who have elevated sputum neutrophils | |||||||||||||
Medical condition: Moderate to severe asthma | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2010-018621-19 | Sponsor Protocol Number: MT-04 | Start Date*: 2011-09-30 | |||||||||||
Sponsor Name:ALK-Abelló A/S | |||||||||||||
Full Title: Efficacy of ALK house dust mite allergy immunotherapy tablet in subjects with house dust mite induced asthma. The MITRA Trial. | |||||||||||||
Medical condition: House dust mite induced allergic asthma | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) DK (Completed) SK (Completed) LT (Completed) ES (Completed) GB (Completed) AT (Completed) NL (Completed) LV (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2007-005094-54 | Sponsor Protocol Number: TPI ASM8-205 | Start Date*: 2008-01-17 | ||||||||||||||||
Sponsor Name:Topigen Pharmaceuticals Inc. | ||||||||||||||||||
Full Title: A MULTICENTER, DOUBLE-BLIND, RANDOMIZED, PLACEBO-CONTROLLED, CROSSOVER STUDY TO EVALUATE THE EFFICACY AND SAFETY OF 14-DAY INHALED TPI ASM8 IN SUBJECTS WITH ASTHMA | ||||||||||||||||||
Medical condition: allergic asthma and allergen-induced asthma | ||||||||||||||||||
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Population Age: Adults | Gender: Male, Female | |||||||||||||||||
Trial protocol: GB (Completed) IT (Completed) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2011-000057-23 | Sponsor Protocol Number: AV-G-01 | Start Date*: 2011-05-26 | ||||||||||||||||
Sponsor Name:ALK-Abello S.A. | ||||||||||||||||||
Full Title: Estudio abierto para valorar la tolerabilidad de la inmunoterapia con AVANZ Phleum pratense | ||||||||||||||||||
Medical condition: Rinoconjuntivitis alérgica con o sin asma debido a la sensibilidad al polen de gramineas. | ||||||||||||||||||
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Population Age: Adults | Gender: Male, Female | |||||||||||||||||
Trial protocol: ES (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2022-002289-33 | Sponsor Protocol Number: 601-0018 | Start Date*: 2023-02-01 | ||||||||||||||||
Sponsor Name:Pulmatrix, Inc. | ||||||||||||||||||
Full Title: A Randomized, Double-Blind, Multicenter, Placebo-Controlled Study to Evaluate the Effect of Dose and Duration of Treatment of Itraconazole Administered as a Dry Powder for Inhalation (PUR1900) on S... | ||||||||||||||||||
Medical condition: Allergic bronchopulmonary aspergillosis (ABPA) in patients with asthma | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: FR (Prematurely Ended) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2011-000674-58 | Sponsor Protocol Number: AL1011av | Start Date*: 2011-07-28 | ||||||||||||||||
Sponsor Name:Allergopharma Joachim Ganzer KG | ||||||||||||||||||
Full Title: Double-blind, placebo controlled study to investigate the dose response of an allergoid preparation of Phleum pratense in adult patients with IgE mediated allergic Rhinitis / Rhinoconjunctivitis wi... | ||||||||||||||||||
Medical condition: ICD classification code: J 45.0 and J 30.1 | ||||||||||||||||||
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Population Age: Adults | Gender: Male, Female | |||||||||||||||||
Trial protocol: DE (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2014-004775-23 | Sponsor Protocol Number: MK-0476-383 | Start Date*: 2015-04-08 |
Sponsor Name:Merck Frosst Canada Ltd. | ||
Full Title: RADAR: SingulaiR® in Asthma anD Allergic Rhinitis An 8 week multicenter, open-label, observational study to evaluate the effectiveness of adding Montelukast Sodium (SINGULAIR®) 10 mg per day to inh... | ||
Medical condition: Adult asthma and allergic rhinitis | ||
Disease: | ||
Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | |
Trial protocol: Outside EU/EEA | ||
Trial results: View results |
EudraCT Number: 2011-000126-30 | Sponsor Protocol Number: ASM8-A-208 | Start Date*: 2011-06-07 | ||||||||||||||||
Sponsor Name:Pharmaxis Ltd | ||||||||||||||||||
Full Title: A phase II, multi-centre, single blind study to evaluate the safety, tolerability and explore the efficacy of 8.0 mg ASM8 inhaled daily for 14 days in adult subjects with moderate to severe asthma | ||||||||||||||||||
Medical condition: moderate to severe asthma | ||||||||||||||||||
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Population Age: Adults | Gender: Male, Female | |||||||||||||||||
Trial protocol: GB (Prematurely Ended) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2013-000487-28 | Sponsor Protocol Number: VO72.12 | Start Date*: 2013-08-20 | ||||||||||||||||
Sponsor Name:STALLERGENES SA | ||||||||||||||||||
Full Title: A dose ranging study investigating the efficacy and safety of sublingual immunotherapy tablets of house dust mite allergen extracts in adults with house dust mite-associated allergic asthma | ||||||||||||||||||
Medical condition: house dust mite-associated allergic asthma | ||||||||||||||||||
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Population Age: Adults | Gender: Male, Female | |||||||||||||||||
Trial protocol: AT (Completed) GB (Completed) SK (Completed) DE (Completed) CZ (Completed) BE (Completed) ES (Ongoing) PL (Completed) BG (Completed) DK (Completed) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2006-003385-34 | Sponsor Protocol Number: CRU.LUMC.001 | Start Date*: 2006-11-23 | |||||||||||
Sponsor Name:Boehringer Ingelheim Pharma GmbH & Co. KG | |||||||||||||
Full Title: The effect of tiotropium-bromide on deep inspiration-induced bronchodilation and airway responsiveness in asthma. | |||||||||||||
Medical condition: 24 patients with mild persistent asthma will participate in the study. All patients will be allergic to one or more airborne allergens, hyperresponsive to histamine (PC20 < 8 mg/ml) and have a norm... | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2016-004363-39 | Sponsor Protocol Number: MT-11 | Start Date*: 2018-03-15 | ||||||||||||||||
Sponsor Name:ALK-Abelló A/S | ||||||||||||||||||
Full Title: A phase III trial evaluating the efficacy and safety of the house dust mite (HDM) sublingual immunotherapy (SLIT)-tablet in children and adolescents (5-17 years) with HDM allergic asthma | ||||||||||||||||||
Medical condition: House Dust Mite (HDM) Allergic Asthma | ||||||||||||||||||
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Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | |||||||||||||||||
Trial protocol: DE (Prematurely Ended) ES (Temporarily Halted) HU (Completed) BG (Completed) DK (Completed) FR (Completed) PL (Completed) GB (GB - no longer in EU/EEA) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2011-000586-12 | Sponsor Protocol Number: MATERIAL | Start Date*: 2011-11-08 | |||||||||||||||||||||
Sponsor Name:Academic Medical Center | |||||||||||||||||||||||
Full Title: The efficacy of mepolizumab treatment on rhinovirus induced asthma exacerbations | |||||||||||||||||||||||
Medical condition: Asthma and more specifically virus-induced exacerbations in allergic asthma patients | |||||||||||||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: NL (Ongoing) | |||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2008-001209-41 | Sponsor Protocol Number: AC-060A201 | Start Date*: 2008-07-25 | |||||||||||
Sponsor Name:Actelion Pharmaceuticals Ltd | |||||||||||||
Full Title: A multi-center, double-blind, placebo-controlled, randomized, multiple dose, 2-period cross-over, Phase IIa study to investigate the pharmacodynamics, tolerability and safety, and pharmacokinetics ... | |||||||||||||
Medical condition: Allergic Asthma | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) NL (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2011-001062-18 | Sponsor Protocol Number: CQAW039A2206 | Start Date*: 2011-09-02 | |||||||||||
Sponsor Name:Novartis Pharma Services AG | |||||||||||||
Full Title: A randomized, placebo-controlled, dose-ranging, multi-centre trial of QAW039 (1-450 mg p.o.), to investigate the effect on FEV1 and ACQ in patients with moderate-to-severe, persistent, allergic ast... | |||||||||||||
Medical condition: Moderate-to-severe, persistent, allergic asthma, inadequately controlled with ICS therapy | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: GR (Completed) GB (Completed) AT (Completed) HU (Completed) PL (Completed) NL (Completed) IT (Completed) BG (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2014-004748-37 | Sponsor Protocol Number: MK-0476-367 | Start Date*: 2015-04-03 |
Sponsor Name:MSD Korea LTD. | ||
Full Title: Korean Study of “Real-world” Montelukast Use in Mild Asthmatic Children with Concomitant Allergic Rhinitis | ||
Medical condition: mild asthma and allergic rhinitis | ||
Disease: | ||
Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | |
Trial protocol: Outside EU/EEA | ||
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: 2007-000047-99 | Sponsor Protocol Number: MK-0476P2181V1 | Start Date*: 2007-03-06 | ||||||||||||||||||||||||||
Sponsor Name:Tari Haahtela | ||||||||||||||||||||||||||||
Full Title: Montelukast as a controller of atopic syndrome - MONTAS-study | ||||||||||||||||||||||||||||
Medical condition: Allergic symptoms (rhinitis, conjunctivits, asthma, oral symptoms and atopic eczema) caused by pollen allergy to birch or timothy. | ||||||||||||||||||||||||||||
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Population Age: Adults | Gender: Male, Female | |||||||||||||||||||||||||||
Trial protocol: FI (Completed) | ||||||||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2009-010914-31 | Sponsor Protocol Number: CHD-PI08 | Start Date*: 2009-12-02 | |||||||||||
Sponsor Name:Dr. Christian Domingo | |||||||||||||
Full Title: Eficacia clínica y cambios histológicos secundarios al tratamiento con omalizumab en asmáticos alérgicos en estadio V de la gina | |||||||||||||
Medical condition: Asma | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2005-003860-47 | Sponsor Protocol Number: CIGE025ADE03 | Start Date*: 2006-02-20 | |||||||||||
Sponsor Name:Novartis Pharma GmbH | |||||||||||||
Full Title: A randomized, 20 week, double-blind, placebo-controlled, parallel-group, multiple-dose, multicenter study to assess the efficacy and safety of Omalizumab in combination with Depigoid, versus Depigo... | |||||||||||||
Medical condition: Asthma extrinsic | |||||||||||||
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Population Age: Adolescents, Under 18, Adults | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: View results |
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