- Trials with a EudraCT protocol (141)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
141 result(s) found for: Allergic Rhinitis AND Allergy AND Asthma.
Displaying page 5 of 8.
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: 2014-003204-70 | Sponsor Protocol Number: DOM-STA-2014-01 | Start Date*: 2015-04-24 |
Sponsor Name:Dr. Javier Domínguez Ortega | ||
Full Title: Pilot study on asthma control in patients with grass- pollen allergic rhinitis treated with 5 grass-pollen sublingual immunotherapy (Staloral®) vs placebo | ||
Medical condition: Respiratory Allergy: Asthma and allergic rhinitis due to grass pollen | ||
Disease: | ||
Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | |
Trial protocol: ES (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2012-001591-11 | Sponsor Protocol Number: 3.4.11.049 | Start Date*: 2012-12-21 |
Sponsor Name:Erasmus MC | ||
Full Title: Symptomatic treatment of pollen related allergic rhinoconjunctivitis and the relation with asthma with children in the General practice | ||
Medical condition: Allergic Rhinitis Asthma | ||
Disease: | ||
Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | |
Trial protocol: NL (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2018-004262-34 | Sponsor Protocol Number: MM09-SIT-023 | Start Date*: 2020-04-28 | |||||||||||||||||||||
Sponsor Name:Inmunotek, S.L. | |||||||||||||||||||||||
Full Title: Randomized, placebo-controlled, prospective clinical trial of efficacy and safety for the treatment of rhinitis/rhinoconjunctivitis and asthma against a mixture of Dermatophagoides pteronyssinus an... | |||||||||||||||||||||||
Medical condition: House dust mites allergy | |||||||||||||||||||||||
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Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: ES (Ongoing) | |||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2011-000870-79 | Sponsor Protocol Number: 101-PG-PSC-186 | Start Date*: 2012-02-17 | |||||||||||
Sponsor Name:Laboratorios LETI, S.L.U. | |||||||||||||
Full Title: Prospective study to evaluate the safety of a 4-month treatment with Depigoid® Dermatophagoides pteronyssinus or 50% Dermatophagoides pteronyssinus / 50% Dermatophagoides farinae (500 DPP/ml) in pa... | |||||||||||||
Medical condition: Allergic rhinitis or rhinoconjunctivitis with or without mild persistent or intermittent asthma, to Dermatophagoides pteronyssinus or Dermatophagoides pteronyssinus and Dermatophagoides farinae. | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2008-006261-81 | Sponsor Protocol Number: PM/0028 | Start Date*: 2009-06-24 | ||||||||||||||||||||||||||
Sponsor Name:HAL Allergy | ||||||||||||||||||||||||||||
Full Title: Dose Tolerability Study with High Dose PURETHAL Mites in Allergic Rhinitis / Rhinoconjunctivitis Patients. An open study to assess tolerability, safety and short-term efficacy of high dose PURETHA... | ||||||||||||||||||||||||||||
Medical condition: Allergic (IgE-mediated) rhinitis / rhinoconjunctivitis triggered by house dust mites. | ||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||
Trial protocol: DE (Completed) | ||||||||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2005-000025-35 | Sponsor Protocol Number: Al0204AV | Start Date*: 2005-04-05 |
Sponsor Name:Allergopharma Joachim Ganzer KG | ||
Full Title: A multicentre randomised placebo-controlled double-blind clinical trial for evaluation of safety and efficacy of specific immunotherapy with an aluminium hydroxide-adsorbed allergoid preparation of... | ||
Medical condition: IgE-mediated allergic diseases including allergic rhinitis/rhinoconjunctivitis, allergic bronchial asthma (GINA I and II) triggered by birch pollen allergens | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: DE (Completed) FI (Completed) SE (Completed) | ||
Trial results: View results |
EudraCT Number: 2018-001339-33 | Sponsor Protocol Number: SCITVITD3 | Start Date*: 2018-07-05 |
Sponsor Name:Academisch medisch centrum Amsterdam | ||
Full Title: A randomized, double-blind, placebo-controlled, study to determine the added value of vitamin D3 to treatment with subcutaneous immunotherapy in patients with moderate to severe allergic rhinitis/ ... | ||
Medical condition: subcutaneous immunotherapy in allergic rhinitis (AR) patients with allergies to birchpollen | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: NL (Completed) | ||
Trial results: (No results available) |
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: 2014-000279-15 | Sponsor Protocol Number: CP009 | Start Date*: 2014-07-03 | |||||||||||
Sponsor Name:Circassia Limited | |||||||||||||
Full Title: A Multi-Centre, Single-Blind Study to Assess the Safety of Cat-PAD in Cat Allergic Paediatric Subjects. | |||||||||||||
Medical condition: Treatment of cat-allergen induced rhinoconjunctivitis in paediatric subjects with clinically relevant symptoms | |||||||||||||
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Population Age: Children, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: PL (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2021-002089-42 | Sponsor Protocol Number: R1908-1909-ALG-2102 | Start Date*: 2021-11-18 | |||||||||||
Sponsor Name:Regeneron Pharmaceuticals, Inc. | |||||||||||||
Full Title: A Randomized, Double-Blind, Placebo-Controlled Study in Cat-Allergic Patients with Allergic Rhinitis Who Live with a Cat to Assess the Efficacy and Safety of Anti-Fel d 1 Antibodies during Natural ... | |||||||||||||
Medical condition: Allergic Rhino conjunctivitis due to Cat Allergy | |||||||||||||
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Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) BE (Prematurely Ended) FR (Prematurely Ended) PL (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2012-000414-11 | Sponsor Protocol Number: 603-PG-PSC-191 | Start Date*: 2012-08-31 | |||||||||||
Sponsor Name:LETI Pharma GmbH | |||||||||||||
Full Title: Multicenter, placebo-controlled, long-term study of Depigoid Birch 5000 in adults and adolescents with allergic rhinitis and/or rhinoconjunctivitis with or without intermittent asthma | |||||||||||||
Medical condition: Seasonal allergic rhinitis and/or rhinoconjunctivitis with or without intermittent asthma due to birch pollen allergy | |||||||||||||
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Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) LT (Completed) CZ (Completed) FI (Completed) PL (Completed) LV (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2006-000359-16 | Sponsor Protocol Number: VD-3 | Start Date*: 2007-04-16 |
Sponsor Name:Ove Bäck, Dept Dermatology, University Hospital, Lund, Sweden | ||
Full Title: Vitamin D and atopic allergy | ||
Medical condition: Cumulative incidence of atopic allergy specified as atopic dermatitis, allergic asthma, and allergic rhinitis. Since IMP is a food supplement to protect from rickets we are looking at clinical sym... | ||
Disease: | ||
Population Age: Infants and toddlers, Children, Under 18 | Gender: Male, Female | |
Trial protocol: SE (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2015-004806-40 | Sponsor Protocol Number: MEIN/15/Bil-ARC/001 | Start Date*: 2016-03-29 |
Sponsor Name:Menarini International Operations Luxembourg S.A. | ||
Full Title: Bilastine and Montelukast in patients with seasonal allergic rhinoconjunctivitis and asthma: Efficacy of concomitant administration - the SKY study; Acronym: SKY | ||
Medical condition: Seasonal allergic rhinoconjunctivitis and asthma | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: SK (Completed) CZ (Completed) PL (Completed) LV (Completed) HR (Completed) IT (Completed) | ||
Trial results: View results |
EudraCT Number: 2017-002911-33 | Sponsor Protocol Number: ABT-gpASIT011 | Start Date*: 2018-12-18 | |||||||||||
Sponsor Name:ASIT biotech S.A. | |||||||||||||
Full Title: A multicentre, international, randomised, double-blind, placebo controlled study to demonstrate the clinical efficacy and safety of subcutaneous immunotherapy with gpASIT+™ in patients with grass p... | |||||||||||||
Medical condition: Treatment of seasonal grass pollen-induced rhinoconjunctivitis | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Prematurely Ended) CZ (Prematurely Ended) HU (Prematurely Ended) BE (Prematurely Ended) PL (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
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: 2006-005868-10 | Sponsor Protocol Number: 6043-PG-PSC-153 | Start Date*: 2007-07-24 | |||||||||||
Sponsor Name:Laboratorios LETI S.L. | |||||||||||||
Full Title: Ensayo clínico, multicéntrico, aleatorizado, doble ciego controlado con placebo, de inmunoterapia subcutánea con extracto despigmentado y polimerizado de polen de Phleum pratense en pacientes con h... | |||||||||||||
Medical condition: Rinoconjuntivitis moderada-severa (con o sin asma episódico) inducida por hipersensibilidad frente al polen de gramíneas. | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Completed) HU (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2014-000172-26 | Sponsor Protocol Number: 1301-PG-PSC-203 | Start Date*: 2014-06-26 | |||||||||||
Sponsor Name:Laboratorios LETI S.L.U | |||||||||||||
Full Title: A multicentre, open label, phase IIb clinical trial to evaluate safety, tolerability and efficacy of the depigmented modified allergen extract of two mites mixes at 200 DPP/ml (DP/MG/14-1 Dermatoph... | |||||||||||||
Medical condition: Allergic rhinitis or rihinoconjuntivitis, with controlled allergic asthma due to D. pteronyssinus and Blomia tropicalis or Lepidoglyphus destructor sensitization. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2011-002317-10 | Sponsor Protocol Number: SC-31A | Start Date*: 2019-04-17 | |||||||||||||||||||||
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 house dust mite 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) |
EudraCT Number: 2011-006251-11 | Sponsor Protocol Number: HLS05/2011 | Start Date*: 2012-03-19 | |||||||||||
Sponsor Name:AZIENDA OSPEDALIERA L. SACCO (A.O. DI RILIEVO NAZIONALE) | |||||||||||||
Full Title: Pilot clinical trial, controlled and randomized, Phase III, to evaluate security and efficacy of oral specific immunotherapy in HIV infected patients who suffer from grass pollen allergy. | |||||||||||||
Medical condition: HIV+ subjects with grass pollen allergy. | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Ongoing) | |||||||||||||
Trial results: (No results available) |
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