- Trials with a EudraCT protocol (427)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
427 result(s) found for: Allergic response.
Displaying page 1 of 22.
| EudraCT Number: 2011-004830-32 | Sponsor Protocol Number: ICPCT-2011-UA-FF | Start Date*: 2012-01-27 | |||||||||||
| Sponsor Name:FAES FARMA, S.A. | |||||||||||||
| Full Title: Effects of bilastine on nasal volume after allergen-induced rhinitis in patients with allergic rhinitis | |||||||||||||
| Medical condition: Allergic Rhinitis | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: ES (Ongoing) | |||||||||||||
| 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: 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: 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: 2013-004720-11 | Sponsor Protocol Number: AV-X-03 | Start Date*: 2014-02-11 | |||||||||||
| Sponsor Name:ALK-Abelló, S.A. | |||||||||||||
| Full Title: An open trial to assess the tolerability of AVANZ® Cupressus immunotherapy | |||||||||||||
| Medical condition: Allergic rhinoconjunctivitis induced by Cupressus arizonica pollen. | |||||||||||||
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| Population Age: Adults | Gender: Male, Female | ||||||||||||
| Trial protocol: ES (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2013-001728-20 | Sponsor Protocol Number: AV-X-02 | Start Date*: 2013-11-13 | |||||||||||
| Sponsor Name:ALK-Abelló S. A. | |||||||||||||
| Full Title: An open trial to assess the tolerability of AVANZ® Salsola immunotherapy | |||||||||||||
| Medical condition: Allergic rhinoconjunctivitis with or without asthma due to sensitisation to Salsola kali pollen | |||||||||||||
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| Population Age: Adults | Gender: Male, Female | ||||||||||||
| Trial protocol: ES (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2011-004852-20 | Sponsor Protocol Number: AV-X-01 | Start Date*: 2012-04-10 | |||||||||||
| Sponsor Name:ALK-Abelló, S.A. | |||||||||||||
| Full Title: An open trial to assess the tolerability of AVANZ Olive immunotherapy | |||||||||||||
| Medical condition: Allergic rhinoconjunctivitis with/without asthma due to sensitization to Olea europaea (olive) pollen | |||||||||||||
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| Population Age: Adults | Gender: Male, Female | ||||||||||||
| Trial protocol: ES (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: 2007-002808-18 | Sponsor Protocol Number: AL0701rP | Start Date*: 2007-10-31 | ||||||||||||||||
| Sponsor Name:ALLERGOPHARMA JOACHIM GANZER KG | ||||||||||||||||||
| Full Title: A double-blind placebo controlled dose-response study for evaluation of safety and efficacy of immunotherapy with a cocktail of recombinant major allergens of Timothy Grass Pollen (Phleum pratense)... | ||||||||||||||||||
| Medical condition: ICD classification code: J45.0 and J30.1 | ||||||||||||||||||
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| Population Age: 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: 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: 2006-002123-17 | Sponsor Protocol Number: 06/Q0404/12 | Start Date*: 2007-10-02 | |||||||||||
| Sponsor Name:Imperial College London | |||||||||||||
| Full Title: Mechanistic study assessing the immunological response of subjects after treatment with different formulations of sublingual immunotherapy. | |||||||||||||
| Medical condition: Patients with seasonal allergic rhinitis to grass pollen | |||||||||||||
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| Population Age: Adults | Gender: Male, Female | ||||||||||||
| Trial protocol: GB (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2011-002319-27 | Sponsor Protocol Number: SL-61A | Start Date*: 2021-02-01 | ||||||||||||||||||||||||||
| Sponsor Name:ROXALL Medizin GmbH | ||||||||||||||||||||||||||||
| Full Title: Phase II study to assess the tolerability, safety and efficacy of sublingual immunotherapy in patients suffering from birch pollen allergy | ||||||||||||||||||||||||||||
| Medical condition: Birch pollen-related allergic rhinitis / rhino-conjunctivitis | ||||||||||||||||||||||||||||
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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: 2012-005035-85 | Sponsor Protocol Number: 2012RC14 | Start Date*: 2013-05-03 | |||||||||||
| Sponsor Name:Tayside Medical Sciences Centre on behalf of University of Dundee & NHS Tayside | |||||||||||||
| Full Title: A proof of concept study in allergic rhinitis, to evaluate the differential effects of doxazosin between single and chronic dosing on nasal airway calibre | |||||||||||||
| Medical condition: Allergic Rhinitis | |||||||||||||
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| Population Age: Adults | Gender: Male, Female | ||||||||||||
| Trial protocol: GB (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: 2006-006710-15 | Sponsor Protocol Number: IPR109764 | Start Date*: 2007-03-23 | |||||||||||
| Sponsor Name:GlaxoSmithKline Research & Development Limited | |||||||||||||
| Full Title: A randomised, single blind, placebo-controlled 5-way crossover trial of single doses of intranasal GSK256066 in subjects with seasonal allergic rhinitis (SAR) | |||||||||||||
| Medical condition: Seasonal Allergic Rhinitis | |||||||||||||
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| Population Age: Adults | Gender: Male, Female | ||||||||||||
| Trial protocol: DE (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2010-022083-12 | Sponsor Protocol Number: SC-11A | Start Date*: 2014-05-15 | ||||||||||||||||
| Sponsor Name:ROXALL Medizin GmbH | ||||||||||||||||||
| Full Title: Evaluation of tolerability and efficacy of subcutaneous cluster-immunotherapy in patients with allergic rhinitis / rhino-conjunctivitis due to grass pollen | ||||||||||||||||||
| Medical condition: Allergic rhinitis / rhino-conjunctivitis | ||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
| Trial protocol: DE (Completed) | ||||||||||||||||||
| Trial results: View results | ||||||||||||||||||
| EudraCT Number: 2011-002296-42 | Sponsor Protocol Number: SC-21A | Start Date*: 2020-01-31 | ||||||||||||||||||||||||||
| Sponsor Name:ROXALL Medizin GmbH | ||||||||||||||||||||||||||||
| Full Title: Phase II study to assess the tolerability, safety and efficacy of subcutaneous cluster-immunotherapy in patients suffering from birch pollen allergy | ||||||||||||||||||||||||||||
| Medical condition: Allergic rhinitis / rhino-conjunctivitis | ||||||||||||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||
| Trial protocol: DE (Completed) | ||||||||||||||||||||||||||||
| Trial results: (No results available) | ||||||||||||||||||||||||||||
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