- Trials with a EudraCT protocol (81)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
81 result(s) found for: Chronic Urticaria.
Displaying page 1 of 5.
EudraCT Number: 2006-003686-13 | Sponsor Protocol Number: P04805-V2.0 | Start Date*: 2007-05-31 | ||||||||||||||||
Sponsor Name:Allergie-Centrum-Charite, Department of Dermatology, Charite - Universitätsmedizin Berlin | ||||||||||||||||||
Full Title: An exploratory phase III, randomised, double blind, therapeutic single dose-related effect, parallel group study to assess and compare the effects of 5mg vs. 20mg Desloratadine on skin lesions in p... | ||||||||||||||||||
Medical condition: Chronic urticaria is characterized by the spontaneous development of wheal and flare type skin reactions. | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: DE (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2020-003018-11 | Sponsor Protocol Number: CQGE031E12301 | Start Date*: 2021-10-12 | |||||||||||||||||||||
Sponsor Name:Novartis Pharma AG | |||||||||||||||||||||||
Full Title: A multi-center, randomized, double-blind, placebo controlled study to investigate the efficacy and safety of ligelizumab (QGE031) in the treatment of Chronic Inducible Urticaria (CINDU) in adolesce... | |||||||||||||||||||||||
Medical condition: Chronic Inducible Urticaria | |||||||||||||||||||||||
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Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: HU (Prematurely Ended) SK (Prematurely Ended) ES (Prematurely Ended) SI (Completed) NL (Prematurely Ended) FR (Prematurely Ended) DE (Prematurely Ended) GR (Completed) IT (Prematurely Ended) BG (Prematurely Ended) AT (Prematurely Ended) | |||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2006-005404-13 | Sponsor Protocol Number: CIGE025ADE05 | Start Date*: 2007-01-23 | |||||||||||
Sponsor Name:Novartis Pharma GmbH | |||||||||||||
Full Title: A randomized, 24-week, double-blind, placebo-controlled, parallel-group, multicenter study to assess the efficacy and safety of Omalizumab in adult patients with chronic urticaria who exhibit IgE a... | |||||||||||||
Medical condition: chronic urticaria | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2010-018716-33 | Sponsor Protocol Number: PHRN09-AM/MUCIS | Start Date*: 2010-10-21 | |||||||||||
Sponsor Name:CHRU de TOURS | |||||||||||||
Full Title: Etude de l'efficacité du méthotrexate en adjonction d'un anti-histaminique H1 dans le traitement de l'urticaire chronique idiopathique sévère réfractaire aux anti-H1 seuls : essai randomisé. | |||||||||||||
Medical condition: urticaire chronique idiopathique sévère | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2010-024113-31 | Sponsor Protocol Number: CUN-OMAL-CU-2010 | Start Date*: 2011-08-08 | |||||||||||
Sponsor Name:Instituto Científico y Tecnológico de Navarra | |||||||||||||
Full Title: Ensayo clínico multicéntrico, doble ciego, controlado con placebo, cruzado (2x2) con aleatorización de la secuencia, para evaluar la eficacia y seguridad de Omalizumab (Xolair®, Novartis) en una nu... | |||||||||||||
Medical condition: Pacientes con urticaria crónica grave que no responden a dosis aprobadas de antihistamínicos | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2018-002308-15 | Sponsor Protocol Number: P160913 | Start Date*: 2018-11-09 | |||||||||||
Sponsor Name:ASSISTANCE PUBLIQUE - HOPITAUX DE PARIS (AP-HP) | |||||||||||||
Full Title: COrticosteroids in acUte uRticAria in emerGency dEpartment | |||||||||||||
Medical condition: Adults patients with isolated acute urticaria presenting to the emergency department | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2011-004254-25 | Sponsor Protocol Number: CIGE025EDE16 | Start Date*: 2012-05-10 | |||||||||||
Sponsor Name:Novartis Pharma GmbH | |||||||||||||
Full Title: A randomized, double-blind, placebo-controlled, multicenter, 28-week treatment study with an 8 week follow-up period to investigate the impact of subcutaneous Omalizumab on quality of life measures... | |||||||||||||
Medical condition: moderate to severe chronic spontaneous urticaria with angioedema | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2009-009498-87 | Sponsor Protocol Number: Q4577g | Start Date*: 2009-06-25 | ||||||||||||||||
Sponsor Name:Genentech, Inc. | ||||||||||||||||||
Full Title: A Phase II, Multicenter, Randomized, Double-Blind, Placebo-Controlled Dose-Ranging Study Of Xolair (Omaluzimab) In Patients With Chronic Idiopathic Urticaria (CIU) Who Remain Symptomatic With Anith... | ||||||||||||||||||
Medical condition: Chronic Idiopathic Urticaria | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: DE (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2006-001245-33 | Sponsor Protocol Number: BILA 2006/UCI | Start Date*: 2006-07-31 | |||||||||||
Sponsor Name:FAES FARMA S.A. | |||||||||||||
Full Title: “Estudio en fase III, doble ciego, randomizado, controlado con placebo, comparativo de la eficacia y seguridad de bilastina 20 mg una vez al día y levocetirizina 5 mg para el tratamiento de la ... | |||||||||||||
Medical condition: Chronic Idiopathic Urticaria | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Completed) DE (Completed) BE (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2010-022864-12 | Sponsor Protocol Number: AA-10-1.01 | Start Date*: 2011-04-20 | ||||||||||||||||||||||||||
Sponsor Name:Medical Faculty, Otto-von-Guericke-University Magdeburg | ||||||||||||||||||||||||||||
Full Title: Effect of Omalizumab (Xolair) on the threshold of degranulation and the composition of intracellular granules in skin mast cells and peripheral basophilic granulocytes before and during omalizumab ... | ||||||||||||||||||||||||||||
Medical condition: Disease to be investigated: 12 patients with severe chronic urticaria (CU) with or without angioedema which continously need medical treatment As a control: 6 patients with atopy syndrome consisti... | ||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||
Trial protocol: DE (Completed) | ||||||||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2005-002749-38 | Sponsor Protocol Number: BT0800NED001 | Start Date*: 2007-07-18 |
Sponsor Name:Barrier Therapeutics nv | ||
Full Title: A randomized, double-blind, placebo-controlled exploratory trial to evaluate a one-week oral treatment with R129160 (60 mg o.d.) in patients with chronic idiopathic urticaria | ||
Medical condition: Chronic Idiopathic Urticaria | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: BE (Completed) CZ (Completed) NL (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2008-005746-22 | Sponsor Protocol Number: AECUDATT | Start Date*: 2009-05-05 | |||||||||||
Sponsor Name:Allergie-Centrum-Charite, Department of Dermatology, Charite - Universitätsmedizin Berlin | |||||||||||||
Full Title: Multi-center, double blind, dose escalating study to compare the effects of 5 mg, 10mg and 20mg of Desloratadine in patients with acquired cold urticaria (ACU) | |||||||||||||
Medical condition: Chronic urticaria is characterized by the spontaneous development of wheal and flare type skin reactions. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2020-000169-17 | Sponsor Protocol Number: D3259C00001 | Start Date*: 2020-12-01 | |||||||||||
Sponsor Name:AstraZeneca AB | |||||||||||||
Full Title: A Phase 2b Multinational, Randomized, Double-blind, Parallel Group, 24-week Placebo-controlled Study with 28-week Extension to Investigate the Use of Benralizumab in Patients with Chronic Spontaneo... | |||||||||||||
Medical condition: chronic spontaneous urticaria | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: BG (Prematurely Ended) DE (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2009-012013-22 | Sponsor Protocol Number: BILA-3009/PED | Start Date*: 2009-12-09 | ||||||||||||||||
Sponsor Name:FAES FARMA S.A. | ||||||||||||||||||
Full Title: A Multicentre, International, Adaptive, Open-label, Repeated Administration Pharmacokinetic Study of Bilastine in Children from 2 to <12 Years of age with Allergic Rhinoconjunctivitis or Chronic Ur... | ||||||||||||||||||
Medical condition: Allergic Rhinoconjunctivitis and chronic urticaria | ||||||||||||||||||
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Population Age: Children, Under 18 | Gender: Male, Female | |||||||||||||||||
Trial protocol: DE (Completed) ES (Completed) SE (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2015-003636-13 | Sponsor Protocol Number: CQGE031C2201E1 | Start Date*: 2016-01-21 | |||||||||||
Sponsor Name:Novartis Pharma Services AG | |||||||||||||
Full Title: An open label, multicenter, extension study to evaluate the long-term safety of QGE031 240 mg s.c. given every 4 weeks for 52 weeks in Chronic Spontaneous Urticaria patients who completed study CQG... | |||||||||||||
Medical condition: Chronic Spontaneous Urticaria | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) ES (Completed) GR (Completed) GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2010-023057-11 | Sponsor Protocol Number: DC02/RUP/3/09 | Start Date*: 2011-02-09 | |||||||||||
Sponsor Name:J. Uriach y Compañía, S.A. | |||||||||||||
Full Title: Efficacy and safety of rupatadine solution in the treatment of Chronic Spontaneous Urticaria (CSU) in paediatric patients (2-11 years old). | |||||||||||||
Medical condition: Treatment of Chronic Spontaneous Urticaria (CSU) in paediatric patients (2-11 years old). | |||||||||||||
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Population Age: Children, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: HU (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2013-003233-15 | Sponsor Protocol Number: GX29107 | Start Date*: 2013-12-02 | |||||||||||
Sponsor Name:Genentech, Inc. | |||||||||||||
Full Title: A multicenter, randomized, double-blind, placebo-controlled pilot study of quilizumab in patients with refractory chronic spontaneous urticaria (CSU). | |||||||||||||
Medical condition: Patients with chronic spontaneous urticaria | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2011-004216-31 | Sponsor Protocol Number: CIGE025E2201 | Start Date*: 2012-03-07 | |||||||||||
Sponsor Name:Novartis Pharma Services AG | |||||||||||||
Full Title: A phase II, multi-centre, randomized, double blind, placebo-controlled study to determine the mode of action of omalizumab in patients with chronic idiopathic urticaria (CIU) who remain symptomatic... | |||||||||||||
Medical condition: Chronic Idiopathic Urticaria | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2004-000771-34 | Sponsor Protocol Number: IC010RUP/3/04 | Start Date*: 2004-10-28 | |||||||||||
Sponsor Name:J. Uriach y Compañía, S.A. | |||||||||||||
Full Title: A 6-week multicentre, double-blind, randomised, placebo-controlled, parallel-group study to assess the efficacy and safety of rupatadine 10 and 20 mg in the treatment of Chronic Idiopathic Urticar... | |||||||||||||
Medical condition: Chronic Idiopathic Urticaria | |||||||||||||
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Population Age: Adolescents, Under 18, Adults | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2020-003756-33 | Sponsor Protocol Number: EFC16720 | Start Date*: 2021-03-25 | |||||||||||
Sponsor Name:Sanofi-aventis recherche et développement | |||||||||||||
Full Title: A randomized, double-blind, placebo-controlled, multi-center, parallel-group study of dupilumab in patients with chronic inducible cold urticaria who remain symptomatic despite the use of H1-antihi... | |||||||||||||
Medical condition: Cold Urticaria | |||||||||||||
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Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: View results |
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