- Trials with a EudraCT protocol (46)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
46 result(s) found for: Skin Diseases AND Hives AND Urticaria.
Displaying page 1 of 3.
| 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: 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: 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: 2014-005559-16 | Sponsor Protocol Number: CQGE031C2201 | Start Date*: 2015-07-17 | |||||||||||
| Sponsor Name:Novartis Pharma Services AG | |||||||||||||
| Full Title: A multicenter, randomized, double-blind, placebo and active-controlled phase 2b dose-finding study of QGE031 as add-on therapy to investigate the efficacy and safety in patients with Chronic Sponta... | |||||||||||||
| Medical condition: Chronic Spontaneous Urticaria | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DE (Completed) ES (Completed) GB (Completed) GR (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: 2011-005615-87 | Sponsor Protocol Number: CIGE025EDE17T | Start Date*: 2012-11-06 | |||||||||||
| Sponsor Name:Allergie-Centrum-Charité, Charité - Universitätsmedizin Berlin | |||||||||||||
| Full Title: A multicenter, randomized, double-blind, placebo-controlled 12-week, parallel-group study with a 6 week follow up period to demonstrate efficacy and safety of subcutaneous Omalizumab in patients wi... | |||||||||||||
| Medical condition: Urticaria factitia | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DE (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| 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: 2016-002273-35 | Sponsor Protocol Number: CIGE025E2306 | Start Date*: 2016-06-02 | |||||||||||
| Sponsor Name:Novartis Pharma Services AG | |||||||||||||
| Full Title: A Multicenter, Randomized, Double-blind, Placebo-controlled Phase III Study to Evaluate the Efficacy and Safety of Omalizumab in Patients With Chronic Spontaneous Urticaria (CSU) Who Remain Symptom... | |||||||||||||
| Medical condition: Chronic Spontaneous Urticaria | |||||||||||||
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| Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: Outside EU/EEA | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2021-003011-26 | Sponsor Protocol Number: BILA-4021/PED | Start Date*: 2021-10-26 | ||||||||||||||||
| Sponsor Name:FAES FARMA S.A. | ||||||||||||||||||
| Full Title: A multicentre, open-label clinical trial to assess plasma levels and safety of bilastine in children from 2 to 5 years of age with seasonal and/or perennial allergic rhinoconjunctivitis or urticaria | ||||||||||||||||||
| Medical condition: Allergic rhinoconjunctivitis. Urticaria. | ||||||||||||||||||
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| Population Age: Children, Under 18 | Gender: Male, Female | |||||||||||||||||
| Trial protocol: SK (Completed) LT (Completed) PL (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: 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: 2010-022785-27 | 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: 2017-004207-52 | Sponsor Protocol Number: CQGE031C2202 | Start Date*: Information not available in EudraCT | |||||||||||
| Sponsor Name:Novartis Pharma AG | |||||||||||||
| Full Title: A multicenter, randomized, double-blind, placebo-controlled phase 2b dose-finding study to investigate the efficacy and safety of ligelizumab (QGE031) in adolescent patients with Chronic Spontaneou... | |||||||||||||
| Medical condition: Chronic Spontaneous Urticaria | |||||||||||||
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| Population Age: Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
| Trial protocol: DE (Completed) ES (Completed) BE (Completed) HU (Completed) EE (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: 2021-006447-95 | Sponsor Protocol Number: CDX0159-07 | Start Date*: 2022-09-09 | |||||||||||
| Sponsor Name:Celldex Therapeutics | |||||||||||||
| Full Title: A Phase 2 Randomized, Double-Blind, Placebo-Controlled, Dose ranging Study to Assess the Efficacy and Safety of CDX-0159 in Patients with Chronic Inducible Urticaria | |||||||||||||
| Medical condition: Chronic Inducible Urticaria | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: EE (Trial now transitioned) DE (Trial now transitioned) PL (Trial now transitioned) ES (Ongoing) LT (Trial now transitioned) HU (Trial now transitioned) LV (Trial now transitioned) BG (Trial now transitioned) | |||||||||||||
| 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 | |||||||||||||
| EudraCT Number: 2016-001505-17 | Sponsor Protocol Number: BILA-3716/PRU | Start Date*: 2016-07-29 | |||||||||||||||||||||
| Sponsor Name:FAES FARMA, S.A. | |||||||||||||||||||||||
| Full Title: An exploratory study to evaluate the efficacy and safety of bilastine in reducing pruritus in patients with chronic spontaneous urticaria and other skin diseases. | |||||||||||||||||||||||
| Medical condition: Chronic spontaneous urticaria and the following skin disorders: 1 - Eczema/dermatitis (acute eczema, chronic eczema, contact dermatitis, atopic dermatitis, nummular eczema, autosensitisation dermat... | |||||||||||||||||||||||
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| Population Age: Elderly | Gender: Male, Female | ||||||||||||||||||||||
| Trial protocol: ES (Completed) HU (Completed) | |||||||||||||||||||||||
| Trial results: View results | |||||||||||||||||||||||
| EudraCT Number: 2021-006413-11 | Sponsor Protocol Number: CDX0159-06 | Start Date*: 2022-07-27 | |||||||||||
| Sponsor Name:Celldex Therapeutics | |||||||||||||
| Full Title: A Phase 2 Randomized, Double-Blind, Placebo-Controlled, Dose-finding Study to Assess the Efficacy and Safety of CDX-0159 in Patients with Chronic Spontaneous Urticaria | |||||||||||||
| Medical condition: Chronic Spontaneous Urticaria | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DE (Completed) HU (Completed) ES (Ongoing) PL (Completed) EE (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| 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: 2021-001796-17 | Sponsor Protocol Number: TV45779-IMB-30086 | Start Date*: 2021-11-30 | |||||||||||
| Sponsor Name:Teva Pharmaceuticals, Inc. | |||||||||||||
| Full Title: A Multinational, Multicenter, Randomized, Double Blind Study to Evaluate the Efficacy, Pharmacokinetics, Pharmacodynamics, Safety, Tolerability, and Immunogenicity of TEV-45779 Compared to Omalizum... | |||||||||||||
| Medical condition: Chronic Idiopathic Urticaria/Chronic Spontaneous Urticaria | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: SK (Completed) CZ (Completed) PL (Completed) GR (Completed) BG (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
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