- Trials with a EudraCT protocol (42)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
42 result(s) found for: alk abello.
Displaying page 2 of 3.
EudraCT Number: 2005-005636-28 | Sponsor Protocol Number: E04/05/PP-M | Start Date*: 2006-08-29 |
Sponsor Name:ALK-ABELLÓ, S.A. | ||
Full Title: Valoración de la eficacia a corto plazo de un extracto de Dermatophagoides pteronyssinus, valorado en unidades de masa y administrado por vía subcutánea, en el tratamiento del asma alérgico. Estudi... | ||
Medical condition: Asma alérgico perenne, con/sin síntomas de rinitis o rinoconjuntivitis, por sensibilización a Dermatophagoides pteronyssinus. | ||
Disease: | ||
Population Age: Adolescents, Under 18, Adults | Gender: Male, Female | |
Trial protocol: ES (Completed) | ||
Trial results: View results |
EudraCT Number: 2013-000492-32 | Sponsor Protocol Number: T16/2013 | Start Date*: 2013-07-10 |
Sponsor Name:Turku University Hospital | ||
Full Title: T cell and interferon expression in tonsils after sublingual immunotherapy and/or nasal live attenuated influenza vaccine | ||
Medical condition: We investigate the effects of allergen and virus on patients with recurrent tonsillitis or tonsillar hypertrphy. | ||
Disease: | ||
Population Age: Children, Adolescents, Under 18, Adults | Gender: Male, Female | |
Trial protocol: FI (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2013-003732-72 | Sponsor Protocol Number: 13IC0847 | Start Date*: 2013-10-14 |
Sponsor Name:Imperial College London | ||
Full Title: Randomised placebo-controlled study of grass pollen allergen immunotherapy tablet (AIT) for seasonal rhinitis: time course of nasal, cutaneous and immunological outcomes | ||
Medical condition: Grass-pollen induced rhinoconjunctivitis (hay fever). | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: GB (Completed) | ||
Trial results: View results |
EudraCT Number: 2009-015381-64 | Sponsor Protocol Number: CRI-2009-09-001-IV | Start Date*: 2009-11-16 | |||||||||||
Sponsor Name:Clinical Research International Ltd. | |||||||||||||
Full Title: "3D-Visualization of the anti-obstructive effect of Levocetirizine" | |||||||||||||
Medical condition: patient with seasonal allergic rhinitis caused by pollen-allergens | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2012-005092-14 | Sponsor Protocol Number: GT-24 | Start Date*: 2013-03-12 | |||||||||||
Sponsor Name:ALK-Abelló S.A. | |||||||||||||
Full Title: Molecular and Cellular Mechanism in the course of Immunotherapy with a Phleum pratense oral lyophilisate | |||||||||||||
Medical condition: Treatment of grass pollen induced rhinitis and conjunctivitis in adult patients with clinically relevant symptoms and diagnosed witha positive skin-prick test and / or specific IgE test to grass po... | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2006-001795-20 | Sponsor Protocol Number: MT-02 | Start Date*: 2006-06-29 |
Sponsor Name:ALK-Abelló A/S | ||
Full Title: A phase II-III trial assessing the efficacy and safety of three doses of the ALK HDM tablet in house dust mite allergic subjects | ||
Medical condition: IgE mediated House dust mite induced mild to moderate asthma and mild to severe allergic rhinitis. | ||
Disease: | ||
Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | |
Trial protocol: SE (Completed) DE (Completed) ES (Completed) DK (Completed) GB (Completed) IT (Completed) | ||
Trial results: View results |
EudraCT Number: 2019-000560-22 | Sponsor Protocol Number: MT-12 | Start Date*: Information not available in EudraCT | |||||||||||
Sponsor Name:ALK-Abelló A/S | |||||||||||||
Full Title: A one-year placebo-controlled phase III trial evaluating the efficacy and safety of the house dust mite (HDM) SLIT-tablet in children (5-11 years of age) with HDM allergic rhinitis/rhinoconjunctivi... | |||||||||||||
Medical condition: Allergic rhinitis/rhinoconjunctivitis induced by house dust mites | |||||||||||||
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Population Age: Children, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Completed) SK (Completed) DE (Completed) PL (Completed) ES (Ongoing) BG (Completed) LT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2020-000446-34 | Sponsor Protocol Number: MT-18 | Start Date*: 2020-07-14 | |||||||||||
Sponsor Name:ALK-Abelló A/S | |||||||||||||
Full Title: A 28-day, single-armed, open-label trial to evaluate safety of the house dust mite (HDM) sublingual allergy immunotherapy (SLIT) tablet in adolescent subjects (12-17 years of age) with HDM allergic... | |||||||||||||
Medical condition: Allergic rhinitis/rhinoconjunctivitis induced by house dust mite | |||||||||||||
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Population Age: Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: SK (Completed) DE (Completed) CZ (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2015-002461-37 | Sponsor Protocol Number: PEPITES | Start Date*: 2015-12-17 | |||||||||||
Sponsor Name:DBV Technologies | |||||||||||||
Full Title: A double-blind, placebo-controlled, randomized phase III pivotal trial to assess the efficacy and safety of peanut epicutaneous immunotherapy with viaskin peanut in peanut-allergic children | |||||||||||||
Medical condition: Peanut Allergy | |||||||||||||
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Population Age: Children, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: IE (Completed) DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2016-002916-42 | Sponsor Protocol Number: PEOPLE-V712-303 | Start Date*: Information not available in EudraCT | |||||||||||
Sponsor Name:DBV TECHNOLOGIES S.A. | |||||||||||||
Full Title: Open-label Follow-up Study of the PEPITES Study to Evaluate the Long-term Efficacy and Safety of Viaskin® Peanut (PEOPLE Study) | |||||||||||||
Medical condition: Peanut Allergy | |||||||||||||
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Population Age: Children, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: IE (Prematurely Ended) DE (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2009-011453-41 | Sponsor Protocol Number: GT-20 | Start Date*: 2009-09-17 | |||||||||||
Sponsor Name:ALK-Abelló S.A. | |||||||||||||
Full Title: Mecanismos moleculares y celulares de rinitis alérgica en pacientes tratados con GRAZAX® -"Molecular and cellular mechanism in rhinitis allergic patients treated with GRAZAX®" | |||||||||||||
Medical condition: Tratamiento de la rinitis y conjuntivitis inducida por polen de gramíneas en pacientes adultos con síntomas clínicamente relevantes y diagnosticados mediante prueba cutánea de prick positiva y/o te... | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2020-005823-35 | Sponsor Protocol Number: 20201206 | Start Date*: 2021-01-28 | |||||||||||||||||||||
Sponsor Name:Aarhus Universitet [...] | |||||||||||||||||||||||
Full Title: ILIT.FT – Dose finding for intralymphatic allergen immunotherapy in a randomized, parallel group, double blind placebo-controlled field trial | |||||||||||||||||||||||
Medical condition: Allergic rhinitis | |||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: DK (Completed) | |||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2018-003456-20 | Sponsor Protocol Number: ITN084AD | Start Date*: 2020-02-17 | |||||||||||
Sponsor Name:Division of Allergy, Immunology, and Transplantation; National Institute of Allergy and Infectious Disease | |||||||||||||
Full Title: Grass Pollen Sublingual Tablet Immunotherapy plus Dupilumab for Induction of Tolerance in Adults with Moderate to Severe Seasonal Allergic Rhinitis. | |||||||||||||
Medical condition: Moderate to Severe Seasonal Allergic Rhinitis | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2009-013429-40 | Sponsor Protocol Number: CVAK694A2205 | Start Date*: 2009-10-15 | |||||||||||
Sponsor Name:Novartis Pharma Services AG | |||||||||||||
Full Title: Randomized, double-blind, placebo-controlled trial to determine the capacity of VAK694 to elicit long term immune tolerance when combined with subcutaneous allergen immunotherapy for the treatment ... | |||||||||||||
Medical condition: Seasonal allergic rhinitis | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2014-001662-94 | Sponsor Protocol Number: TH005 | Start Date*: 2014-09-16 | |||||||||||
Sponsor Name:Circassia Ltd. | |||||||||||||
Full Title: A Double-Blind, Randomised, Placebo-Controlled, Multi-Centre Field Study to Assess the Efficacy and Safety of HDM-SPIRE in Subjects with a History of House Dust Mite-Induced Rhinoconjunctivitis | |||||||||||||
Medical condition: House Dust Mite-Induced Rhinoconjunctivitis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) DE (Completed) NL (Completed) LT (Completed) LV (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2012-001733-13 | Sponsor Protocol Number: CP007 | Start Date*: 2012-10-04 | |||||||||||
Sponsor Name:Circassia Limited | |||||||||||||
Full Title: A Double Blind, Randomised, Placebo Controlled Multi-Centre Field Study to Assess the Efficacy and Safety of Cat-PAD Peptide Immunotherapy in Cat Allergic Subjects | |||||||||||||
Medical condition: Treatment of cat allergen induced rhinoconjunctivitis in patients with clinically relevant symptoms | |||||||||||||
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Population Age: Adolescents, Under 18, Adults | Gender: Male, Female | ||||||||||||
Trial protocol: PL (Completed) BE (Completed) CZ (Completed) DE (Completed) HU (Completed) SK (Completed) LT (Prematurely Ended) LV (Prematurely Ended) EE (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2009-011235-12 | Sponsor Protocol Number: GT-21 | Start Date*: 2009-10-30 | |||||||||||
Sponsor Name:ALK-Abelló A/S | |||||||||||||
Full Title: GAP Grazax Asthma Prevention | |||||||||||||
Medical condition: To prevent development of asthma - The aim of the trial is to investigate whether three consecutive years of treatment with Grazax (75.000 SQ-T) reduces the risk of developing asthma in children co... | |||||||||||||
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Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Completed) DE (Completed) FI (Completed) DK (Completed) GB (Completed) SE (Completed) AT (Completed) ES (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2008-000196-23 | Sponsor Protocol Number: SLO-AD-1 Italy | Start Date*: 2008-10-14 | |||||||||||||||||||||
Sponsor Name:ALK-ABELLO' | |||||||||||||||||||||||
Full Title: Efficacy of sublingual immunotherapy with HDM mix extract (Der p and Der f) (SLITone) in pediatric subjects with mild-to-moderate atopic eczema (AE) and sensitization to HDM (SPT positive). | |||||||||||||||||||||||
Medical condition: Moderate/severe persistent Atopic Eczema (SCORAD >8 and <40)in patients sentitized to HDM | |||||||||||||||||||||||
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Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: IT (Completed) | |||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2010-019373-15 | Sponsor Protocol Number: 291202BS | Start Date*: 2010-06-15 | |||||||||||||||||||||
Sponsor Name:Marinomed Biotechnologie GmbH | |||||||||||||||||||||||
Full Title: A phase IIa, single-center, randomized, reference-controlled, observer-blind trial to assess the efficacy of a topical Aescin formulation in experimentally induced itch, wheal and flare reactions i... | |||||||||||||||||||||||
Medical condition: subjects with proven type I allergy against one of the three allergens: grass pollen, tree pollen, cat epithelia | |||||||||||||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: DE (Completed) | |||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2020-001060-28 | Sponsor Protocol Number: 2020-001060-28 | Start Date*: 2021-03-16 | |||||||||||||||||||||
Sponsor Name:Aarhus Universitet | |||||||||||||||||||||||
Full Title: Documentation of efficacy for intralymphatic allergen immunotherapy in a phase III randomized, parallel group, double blind placebo-controlled multisite field trial | |||||||||||||||||||||||
Medical condition: Allergic rhinitis | |||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: DK (Completed) SE (Completed) | |||||||||||||||||||||||
Trial results: (No results available) |
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