- Trials with a EudraCT protocol (673)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (7)
673 result(s) found for: Allergic disease.
Displaying page 1 of 34.
EudraCT Number: 2007-006099-12 | Sponsor Protocol Number: TSO-01 | Start Date*: 2007-12-21 | |||||||||||
Sponsor Name:Statens Serum Institut | |||||||||||||
Full Title: Oral treatment of allergy with a non-pathogenic microorganism: A randomised clinical trial | |||||||||||||
Medical condition: Allergic rhinitis | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2010-021361-69 | Sponsor Protocol Number: DC01/RUP/2/09 | Start Date*: 2010-09-13 | |||||||||||
Sponsor Name:J. Uriach y Compañía, S.A. | |||||||||||||
Full Title: A multicenter, open-label study to assess pharmacokinetics, efficacy, tolerability and safety of Rupatadine in paediatrics patients (2-5 years old) with allergic rhinitis. | |||||||||||||
Medical condition: Allergic Rhinitis | |||||||||||||
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Population Age: Children, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: HU (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2012-005227-33 | Sponsor Protocol Number: PILIT_2013 | Start Date*: 2013-03-22 | ||||||||||||||||
Sponsor Name:Department of Respiratory Diseases, Aarhus University Hospital | ||||||||||||||||||
Full Title: Effect of Intralymphatic Immunotherapy on Basophil Response and Plasma Cell Kinetics in Allergic Patients | ||||||||||||||||||
Medical condition: allergic rhino-conjunctivitis | ||||||||||||||||||
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Population Age: Adults | Gender: Male, Female | |||||||||||||||||
Trial protocol: DK (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2008-004331-38 | Sponsor Protocol Number: olux 01/08 | Start Date*: 2008-08-28 | |||||||||||
Sponsor Name:MIPHARM | |||||||||||||
Full Title: Randomized study on the effectiveness, safety and acceptability 'of clobetasol propionate foam-cooled (OLUX) in comparison with cream aceponato methylprednisolone in the treatment of allergic conta... | |||||||||||||
Medical condition: Patients suffering from mild to moderate DAC with interest of body surface area not exceeding 20% | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2011-002277-38 | Sponsor Protocol Number: MT-06 | Start Date*: 2011-10-06 | |||||||||||||||||||||
Sponsor Name:ALK-Abelló A/S | |||||||||||||||||||||||
Full Title: A one-year trial evaluating the efficacy and safety of the ALK house dust mite allergy immunotherapy tablet in adult subjects with house dust mite allergic rhinitis | |||||||||||||||||||||||
Medical condition: allergic rhinitis | |||||||||||||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: DE (Completed) CZ (Completed) LV (Completed) DK (Completed) AT (Completed) | |||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2013-004920-12 | Sponsor Protocol Number: PRO-2013 | Start Date*: 2014-02-12 | |||||||||||||||||||||
Sponsor Name:LETI Pharma GmbH | |||||||||||||||||||||||
Full Title: Non-interventional Study in Allergic Patients Suffering from Grass Pollen Induced Rhinitis/Rhinoconjunctivitis with or without Asthma. Retrospective Assessment of the Efficacy of a Perennial Speci... | |||||||||||||||||||||||
Medical condition: Allergic rhinitis/rhinoconjunctivitis with or without concomitant asthma due to grass pollen allergy | |||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: CZ (Completed) | |||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2021-002881-42 | Sponsor Protocol Number: SL-351A | Start Date*: 2023-02-07 | ||||||||||||||||||||||||||
Sponsor Name:ROXALL Medizin GmbH | ||||||||||||||||||||||||||||
Full Title: Phase II study to assess the tolerability, safety and efficacy of sublingual immunotherapy in patients suffering from grass pollen allergy | ||||||||||||||||||||||||||||
Medical condition: Patients with grass pollen-related allergic rhinitis/rhino-conjunctivitis (with well-controlled mild-to-moderate or without asthma) | ||||||||||||||||||||||||||||
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Population Age: Adults | Gender: Male, Female | |||||||||||||||||||||||||||
Trial protocol: DE (Completed) | ||||||||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2017-000754-19 | Sponsor Protocol Number: AL1602av | Start Date*: 2017-11-09 | |||||||||||||||||||||||||||||||
Sponsor Name:Allergopharma GmbH & Co. KG | |||||||||||||||||||||||||||||||||
Full Title: A multicentre, randomized, open label clinical trial for safety evaluation of an accelerated high dose escalation schedule with one strength for an allergen immunotherapy with an aluminium hydroxid... | |||||||||||||||||||||||||||||||||
Medical condition: Patients with moderate to severe seasonal rhinitis or rhinoconjunctivitis with or without asthma | |||||||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||||||||||||
Trial protocol: DE (Completed) ES (Completed) 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: 2007-003403-13 | Sponsor Protocol Number: CQAX576A2104 | Start Date*: 2007-12-19 | |||||||||||
Sponsor Name:Novartis Pharma Services AG | |||||||||||||
Full Title: A proof of concept study of the effects of QAX576 (an interleukin-13 monoclonal antibody) on allergic inflammation following out of allergy season repeated nasal allergen challenge in subjects with... | |||||||||||||
Medical condition: Seasonal allergic rhinitis | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2015-005400-28 | Sponsor Protocol Number: AL1502AV | Start Date*: 2016-06-20 | |||||||||||||||||||||||||||||||
Sponsor Name:Allergopharma GmbH & Co. KG | |||||||||||||||||||||||||||||||||
Full Title: Open label phase II multicenter clinical trial to evaluate safety during accelerated dose escalation of an allergoid birch pollen preparation in patients with IgE mediated allergic rhinitis or rhin... | |||||||||||||||||||||||||||||||||
Medical condition: Patients with seasonal rhinitis or rhinoconjunctivitis with or without controlled asthma during the birch pollen season | |||||||||||||||||||||||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||||||||||||||||||||||
Trial protocol: DE (Completed) | |||||||||||||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2015-002409-13 | Sponsor Protocol Number: AL1501AV | Start Date*: 2015-11-19 | |||||||||||||||||||||||||||||||
Sponsor Name:Allergopharma GmbH & Co. KG | |||||||||||||||||||||||||||||||||
Full Title: A multicenter, randomized, open-label clinical trial to evaluate safety and tolerability of a year-round initiation of specific immunotherapy with an aluminum hydroxide adsorbed allergoid preparati... | |||||||||||||||||||||||||||||||||
Medical condition: Patients with moderate to severe seasonal rhinitis or rhinoconjunctivitis with or without controlled asthma. | |||||||||||||||||||||||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||||||||||||||||||||||
Trial protocol: DE (Completed) | |||||||||||||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2017-003953-41 | Sponsor Protocol Number: C-09-50 | Start Date*: 2017-11-22 | |||||||||||
Sponsor Name:Alcon Research Ltd | |||||||||||||
Full Title: An Open-label, Long-term Study, with AL-4943A Ophthalmic Solution, 0.2% in Patients with Allergic Conjunctivitis | |||||||||||||
Medical condition: Allergic conjunctivitis | |||||||||||||
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Population Age: Adolescents, Under 18, Adults | Gender: Male, Female | ||||||||||||
Trial protocol: Outside EU/EEA | |||||||||||||
Trial results: View results |
EudraCT Number: 2020-004372-17 | Sponsor Protocol Number: TT-06 | Start Date*: 2021-04-20 | ||||||||||||||||
Sponsor Name:ALK-Abelló A/S | ||||||||||||||||||
Full Title: Efficacy and safety of the SQ tree sublingual immunotherapy tablet in children and adolescents (5 through 17 years of age) with moderate to severe allergic rhinitis and/or conjunctivitis induced by... | ||||||||||||||||||
Medical condition: Tree pollen induced allergic rhinitis and/or conjuctivitis. | ||||||||||||||||||
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Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | |||||||||||||||||
Trial protocol: DE (Completed) LT (Completed) HU (Completed) SK (Completed) PL (Completed) AT (Completed) DK (Completed) BE (Completed) NL (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2007-005301-22 | Sponsor Protocol Number: IPR110723 | Start Date*: 2008-02-07 | |||||||||||
Sponsor Name:GlaxoSmithKline Research & Development Limited | |||||||||||||
Full Title: An 8 day, randomised, double blind, 3-way crossover trial of repeat doses of intranasal GSK256066 and fluticasone propionate in the Vienna Challenge Chamber in subjects with seasonal allergic rhini... | |||||||||||||
Medical condition: Seasonal allergic rhinitis | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: AT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2005-005340-12 | Sponsor Protocol Number: IPR101987 | Start Date*: 2006-03-23 | |||||||||||
Sponsor Name:GlaxoSmithKline Research & Development Limited | |||||||||||||
Full Title: A 14 day, randomised, double blinded, placebo-controlled 2-way crossover trial of repeat doses of intranasal GSK256066 and placebo in an environmental exposition unit (Vienna Challenge Chamber) in ... | |||||||||||||
Medical condition: Seasonal Allergic Rhinitis | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: AT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2013-003689-15 | Sponsor Protocol Number: StopEAA | Start Date*: 2015-01-21 | |||||||||||
Sponsor Name:Klinikum der Universität München | |||||||||||||
Full Title: Stop exogenous allergic alveolitis (EAA) in childhood: healthy into adulthood – a randomized, double-blind, placebo-controlled, parallel-group study to evaluate prednisolone treatment and course of... | |||||||||||||
Medical condition: exogenous allergic alveolitis (EAA) | |||||||||||||
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Population Age: Children, Adolescents, Under 18, Adults | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2021-006533-19 | Sponsor Protocol Number: SC-312A | Start Date*: 2022-11-15 | ||||||||||||||||
Sponsor Name:ROXALL Medizin GmbH | ||||||||||||||||||
Full Title: Phase II-III study to assess the efficacy and safety of subcutaneous cluster-immunotherapy in patients suffering from grass pollen allergy | ||||||||||||||||||
Medical condition: Patients with grass pollen-related allergic rhinitis/rhinoconjunctivitis and well-controlled mild-to-moderate or without asthma | ||||||||||||||||||
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Population Age: Adults | Gender: Male, Female | |||||||||||||||||
Trial protocol: DE (Completed) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2006-006000-11 | Sponsor Protocol Number: IPR107498 | Start Date*: 2007-01-01 | |||||||||||
Sponsor Name:GlaxoSmithKline Research & Development Limited | |||||||||||||
Full Title: An 8 day, randomised, double blinded, placebo-controlled 2-way crossover trial of repeat doses of intranasal GSK256066 and placebo in the Vienna Challenge Chamber in subjects with seasonal allergic... | |||||||||||||
Medical condition: Seasonal allergic rhinitis | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: AT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2008-006292-77 | Sponsor Protocol Number: SB/0027 | Start Date*: 2009-05-08 | ||||||||||||||||||||||||||
Sponsor Name:HAL Allergy | ||||||||||||||||||||||||||||
Full Title: SUBLIVAC® Birch PROBE study | ||||||||||||||||||||||||||||
Medical condition: IgE mediated allergic disorders triggered by birch pollen | ||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||
Trial protocol: DE (Completed) | ||||||||||||||||||||||||||||
Trial results: View results |
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