- Trials with a EudraCT protocol (56)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
56 result(s) found for: Angioedema and urticaria.
Displaying page 1 of 3.
| 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: 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: 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: 2012-001670-28 | Sponsor Protocol Number: BER-1272-0058-I | Start Date*: 2013-03-18 | |||||||||||
| Sponsor Name:Medizinische Fakultät der Technischen Universität München | |||||||||||||
| Full Title: Angiotensin Converting Enzyme Inhibitor (ACE) Induced Angioedema BERINERT Randomized, double-blind, two arms, multicenter, Phase III study of Berinert for treatment of ACE induced Angioedema | |||||||||||||
| Medical condition: Angiotensin – Converting – Enzyme – Inhibitors (ACEi) are used in the treatment of several types of cardiovascular and renal diseases. A known side effect of ACEi are angioedema of the head and ... | |||||||||||||
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| Population Age: Adults | Gender: Male, Female | ||||||||||||
| Trial protocol: DE (Prematurely Ended) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2014-001213-12 | Sponsor Protocol Number: HGT-FIR-096 | Start Date*: 2014-09-05 | |||||||||||
| Sponsor Name:Shire Orphan Therapies, Inc. | |||||||||||||
| Full Title: A Phase III, Randomized, Double-Blind, Placebo-Controlled, Multicenter Clinical Study Evaluating the Safety and Efficacy of Icatibant as a Treatment for Angiotensin-Converting Enzyme Inhibitor (ACE... | |||||||||||||
| Medical condition: ACE-I-induced angioedema | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: GB (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: 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: 2019-001703-20 | Sponsor Protocol Number: SHP643-303 | Start Date*: 2020-08-28 | |||||||||||
| Sponsor Name:Dyax Corporation, a Takeda company | |||||||||||||
| Full Title: A Phase 3, Multicenter, Randomized, Placebo-controlled, Double-blind Study to Evaluate the Efficacy and Safety of Lanadelumab for Prevention Against Acute Attacks of Non-histaminergic Angioedema wi... | |||||||||||||
| Medical condition: non-histaminergic angioedema with normal C1-INH and acquired angioedema due to C1-INH deficiency | |||||||||||||
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| Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: GB (GB - no longer in EU/EEA) DE (Completed) HU (Completed) PL (Completed) IT (Completed) FR (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2011-000369-11 | Sponsor Protocol Number: 0624-203 | Start Date*: 2011-07-07 | |||||||||||
| Sponsor Name:ViroPharma Incorporated | |||||||||||||
| Full Title: Open-label, single-dose study to evaluate the response and pharmacokinetics/pharmacodynamics of different doses of Cinryze® [C1 Inhibitor (human)] for treatment of acute angioedema attacks in child... | |||||||||||||
| Medical condition: Acute angioedema attacks in children less than 12 years of age with hereditary angioedema. | |||||||||||||
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| Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
| Trial protocol: HU (Completed) DE (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| 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: 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: 2019-004823-20 | Sponsor Protocol Number: TAK-743-3001 | Start Date*: 2021-07-22 | |||||||||||
| Sponsor Name:Takeda Development Center Americas (TDCA) | |||||||||||||
| Full Title: An Open-Label Study to Evaluate the Long-Term Safety and Efficacy of Lanadelumab for Prevention Against Acute Attacks of Non-histaminergic Angioedema with Normal C1-Inhibitor (C1-INH) | |||||||||||||
| Medical condition: non-histaminergic angioedema with normal C1-INH | |||||||||||||
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| Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DE (Completed) HU (Completed) PL (Completed) NL (Completed) IT (Completed) FR (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: 2010-022785-27 | Sponsor Protocol Number: Q4882g | Start Date*: Information not available in EudraCT | |||||||||||
| Sponsor Name:Genentech, Inc. | |||||||||||||
| Full Title: A PHASE III, MULTICENTER, RANDOMIZED, DOUBLE-BLIND, DOSE-RANGING, PLACEBO-CONTROLLED STUDY TO Evaluate the efficacy, RESPONSE DURATION and safety OF XOLAIR (OMALIZUMAB) IN PATIENTS WITH CHRONIC IDI... | |||||||||||||
| Medical condition: CHRONIC IDIOPATHIC URTICARIA (CIU) | |||||||||||||
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| Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: FR (Ongoing) DE (Completed) DK (Completed) IT (Completed) ES (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2010-022782-99 | Sponsor Protocol Number: Q4881g | Start Date*: Information not available in EudraCT | |||||||||||
| Sponsor Name:Genentech, Inc. | |||||||||||||
| Full Title: A PHASE III, MULTICENTER, RANDOMIZED, DOUBLE-BLIND, PLACEBO-CONTROLLED, DOSE-RANGING STUDY TO Evaluate the efficacy and safety OF XOLAIR (OMALIZUMAB) IN PATIENTS WITH CHRONIC IDIOPATHIC URTICARIA (... | |||||||||||||
| Medical condition: CHRONIC IDIOPATHIC URTICARIA (CIU) | |||||||||||||
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| Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: FR (Ongoing) DE (Completed) DK (Completed) IT (Completed) ES (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2010-022784-35 | Sponsor Protocol Number: Q4883g | Start Date*: 2011-08-08 | |||||||||||
| Sponsor Name:Genentech, Inc. | |||||||||||||
| Full Title: A PHASE III, MULTICENTER, RANDOMIZED, DOUBLE-BLIND, PLACEBO-CONTROLLED SAFETY STUDY OF XOLAIR (OMALIZUMAB) IN PATIENTS WITH CHRONIC IDIOPATHIC URTICARIA (CIU) WHO REMAIN SYMPTOMATIC DESPITE TREATME... | |||||||||||||
| Medical condition: CHRONIC IDIOPATHIC URTICARIA (CIU) | |||||||||||||
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| Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: GB (Completed) DE (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2014-005424-97 | Sponsor Protocol Number: CIGE025EFR02 | Start Date*: 2015-01-28 | |||||||||||
| Sponsor Name:NOVARTIS PHARMA SAS | |||||||||||||
| Full Title: A phase IV, multicenter, single-arm and open-label study to explore the impact on quality of life of omalizumab (Xolair®) in patients with chronic spontaneous urticaria (CSU) who remain symptomatic... | |||||||||||||
| Medical condition: chronic spontaneous urticaria | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: FR (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2006-001449-33 | Sponsor Protocol Number: PO4849 | Start Date*: 2007-07-18 | |||||||||||
| Sponsor Name:Schering Plough Research Institute (SPRI), A Division of Schering Corporation | |||||||||||||
| Full Title: A study of the efficacy, safety, and quality of life (QOL) in patients with chronic idiopathic urticaria dosed with AERIUS Tablets (5 mg, 10 mg, or 20 mg once daily). | |||||||||||||
| Medical condition: Subjects with an active episode of chronic idiopathic urticaria (CIU) and are taking a second-generation antihistamine will be selected for the study. The urticaria activity score (UAS) must be be... | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DE (Completed) ES (Completed) CZ (Completed) SK (Completed) SE (Completed) GR (Completed) IT (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: 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) | |||||||||||||
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