- Trials with a EudraCT protocol (177)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
177 result(s) found for: Seasonal Allergy.
Displaying page 1 of 9.
EudraCT Number: 2012-000672-42 | Sponsor Protocol Number: BIA-STD-003 | Start Date*: 2012-10-11 | |||||||||||||||||||||
Sponsor Name:Bial Industrial Farmacéutica S.A. | |||||||||||||||||||||||
Full Title: Biological standardization of allergen extracts of pollen of Artemisa vulgaris and Platanus acerifolia and the acarus Dermatophagoides farinae in patients sensitized to them. | |||||||||||||||||||||||
Medical condition: Treatment and diagnosis of allergy to Artemisa vulgaris, Platanus acerifolia and Dermatophagoides farinae. | |||||||||||||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: ES (Ongoing) | |||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2010-018786-33 | Sponsor Protocol Number: AlRhi-IIa | Start Date*: 2010-08-05 | |||||||||||
Sponsor Name:Bionorica SE | |||||||||||||
Full Title: A randomized, double-blind, placebo-controlled, cross-over phase IIa/b study to assess the efficacy and safety of 2 dosages of a herbal medicinal product (dry extract BNO-1355) in patients with sea... | |||||||||||||
Medical condition: Seasonal allergic rhinitis | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2011-001371-39 | Sponsor Protocol Number: MP4006 | Start Date*: 2011-03-30 | |||||||||||
Sponsor Name:Meda Pharmaceuticals Inc. | |||||||||||||
Full Title: Randomized, Double-Blind Trial of MP29-02 Nasal Spray Compared to Placebo, Azelastine Hydrochloride Nasal Spray and Fluticasone Propionate Nasal Spray in the Treatment of Patients with Seasonal All... | |||||||||||||
Medical condition: treatment of seasonal allergic rhinitis | |||||||||||||
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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: 2017-003856-22 | Sponsor Protocol Number: C-07-01 | Start Date*: 2017-11-07 | |||||||||||
Sponsor Name:Alcon Research Ltd | |||||||||||||
Full Title: Safety and Efficacy of Olopatadine Hydrochloride Nasal Spray in 6-11 Year old Patients. | |||||||||||||
Medical condition: Seasonal Allergic Rhinitis | |||||||||||||
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Population Age: Children, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: Outside EU/EEA | |||||||||||||
Trial results: View results |
EudraCT Number: 2010-023176-12 | Sponsor Protocol Number: BTT-gpASIT005 | Start Date*: 2010-12-14 | |||||||||||
Sponsor Name:Biotech Tools sa | |||||||||||||
Full Title: Clinical efficacy, immunogenicity, clinical tolerability and assessment of safety of gpASIT+TM administered orally, according to two administration schedules, for the prophylaxis of seasonal grass ... | |||||||||||||
Medical condition: Treatment of seasonal grass pollen rhinoconjunctivitis | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2008-002277-13 | Sponsor Protocol Number: KLF/K/01607 | Start Date*: 2009-07-31 | ||||||||||||||||
Sponsor Name:MCM Klosterfrau Vertriebs GmbH | ||||||||||||||||||
Full Title: Double blind, randomized, placebo-controlled clinical trial to proof the efficacy and tolerability of the homeopathic medicinal product Klosterfrau Allergin Globuli in comparison to placebo in chil... | ||||||||||||||||||
Medical condition: Allergic rhinitis | ||||||||||||||||||
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Population Age: Children, Under 18 | Gender: Male, Female | |||||||||||||||||
Trial protocol: DE (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2006-006710-15 | Sponsor Protocol Number: IPR109764 | Start Date*: 2007-03-23 | |||||||||||
Sponsor Name:GlaxoSmithKline Research & Development Limited | |||||||||||||
Full Title: A randomised, single blind, placebo-controlled 5-way crossover trial of single doses of intranasal GSK256066 in subjects with seasonal allergic rhinitis (SAR) | |||||||||||||
Medical condition: Seasonal Allergic Rhinitis | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2007-005301-22 | Sponsor Protocol Number: IPR110723 | Start Date*: 2008-02-07 | |||||||||||
Sponsor Name:GlaxoSmithKline Research & Development Limited | |||||||||||||
Full Title: An 8 day, randomised, double blind, 3-way crossover trial of repeat doses of intranasal GSK256066 and fluticasone propionate in the Vienna Challenge Chamber in subjects with seasonal allergic rhini... | |||||||||||||
Medical condition: Seasonal allergic rhinitis | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: AT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2006-006000-11 | Sponsor Protocol Number: IPR107498 | Start Date*: 2007-01-01 | |||||||||||
Sponsor Name:GlaxoSmithKline Research & Development Limited | |||||||||||||
Full Title: An 8 day, randomised, double blinded, placebo-controlled 2-way crossover trial of repeat doses of intranasal GSK256066 and placebo in the Vienna Challenge Chamber in subjects with seasonal allergic... | |||||||||||||
Medical condition: Seasonal allergic rhinitis | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: AT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2011-001369-42 | Sponsor Protocol Number: MP4002 | Start Date*: 2011-03-30 | |||||||||||
Sponsor Name:Meda Pharmaceuticals Inc. | |||||||||||||
Full Title: Randomized, Double-Blind Trial of MP29-02 Nasal Spray Compared to Placebo, Azelastine Hydrochloride Nasal Spray, and Fluticasone Propionate Nasal Spray in the Treatment of Patients with Seasonal Al... | |||||||||||||
Medical condition: treatment of seasonal allergic rhinitis | |||||||||||||
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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: 2011-001370-26 | Sponsor Protocol Number: MP4004 | Start Date*: 2011-03-30 | |||||||||||
Sponsor Name:Meda Pharmaceuticals Inc. | |||||||||||||
Full Title: Randomized, Double-Blind Trial of MP29-02 Nasal Spray Compared to Placebo, Azelastine Hydrochloride Nasal Spray, and Fluticasone Propionate Nasal Spray in the Treatment of Patients with Seasonal Al... | |||||||||||||
Medical condition: treatment of seasonal allergic rhinitis | |||||||||||||
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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: 2020-005388-30 | Sponsor Protocol Number: T525-STD-043 | Start Date*: 2022-11-21 | |||||||||||
Sponsor Name:Inmunotek, S.L. | |||||||||||||
Full Title: Quercus ilex and Quercus robur allergenic extracts. Determination of the in vivo allergenic potency in histamine equivalent units (HEP). | |||||||||||||
Medical condition: Allergy to Quercus ilex and Quercus robur pollen | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2020-005389-32 | Sponsor Protocol Number: T521-STD-044 | Start Date*: 2023-03-13 | |||||||||||
Sponsor Name:Inmunotek, S.L. | |||||||||||||
Full Title: Juniperus oxycedrus and Cupressus arizonica allergen extracts. Determination of the in vivo allergenic potency in histamine equivalent units (HEP). | |||||||||||||
Medical condition: Allergy to Cupressaceae: Juniperus oxycedrus and Cupressus arizonica | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2012-000594-24 | Sponsor Protocol Number: 12/014/TAR | Start Date*: 2012-04-19 | |||||||||||
Sponsor Name:Royal Sussex County Hospital | |||||||||||||
Full Title: An open study to investigate the effects of injection immunotherapy on allergen-specific T and B cell responses in adult patients with seasonal allergic rhinitis. | |||||||||||||
Medical condition: Allergic Rhinitis due to birch or grass pollen | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2005-005340-12 | Sponsor Protocol Number: IPR101987 | Start Date*: 2006-03-23 | |||||||||||
Sponsor Name:GlaxoSmithKline Research & Development Limited | |||||||||||||
Full Title: A 14 day, randomised, double blinded, placebo-controlled 2-way crossover trial of repeat doses of intranasal GSK256066 and placebo in an environmental exposition unit (Vienna Challenge Chamber) in ... | |||||||||||||
Medical condition: Seasonal Allergic Rhinitis | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: AT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2011-001314-34 | Sponsor Protocol Number: MP4001 | Start Date*: 2011-03-30 | |||||||||||
Sponsor Name:MedPointe Pharmaceuticals | |||||||||||||
Full Title: Randomized, Double-Blind Trial of MP29-02 Nasal Spray Compared to Placebo, Astelin Nasal Spray, and Fluticasone Propionate Nasal Spray in the Treatment of Subjects with Seasonal Allergic Rhinitis | |||||||||||||
Medical condition: treatment of seasonal allergic rhinitis | |||||||||||||
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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: 2006-002123-17 | Sponsor Protocol Number: 06/Q0404/12 | Start Date*: 2007-10-02 | |||||||||||
Sponsor Name:Imperial College London | |||||||||||||
Full Title: Mechanistic study assessing the immunological response of subjects after treatment with different formulations of sublingual immunotherapy. | |||||||||||||
Medical condition: Patients with seasonal allergic rhinitis to grass pollen | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2008-007657-12 | Sponsor Protocol Number: ParLais/09 | Start Date*: 2009-10-26 | |||||||||||
Sponsor Name:LOFARMA | |||||||||||||
Full Title: Evaluating the efficacy, safety, tolerability of use and treatment adherence in two different dosing schedules, pre-costagionale and costagionale, of a sublingual allergoid (Lais Parietaria)adminis... | |||||||||||||
Medical condition: Subjects with Parietaria pollen allergy. | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2016-003341-28 | Sponsor Protocol Number: PARA_003 | Start Date*: 2016-11-14 | |||||||||||
Sponsor Name:Paradigm Biopharmaceuticals | |||||||||||||
Full Title: A phase 2, randomised, double-blind, placebo-controlled, crossover study to evaluate the effects of a topical pentosan polysulphate sodium (PPS) formulation in subjects with seasonal allergic rhinitis | |||||||||||||
Medical condition: Seasonal allergic rhinitis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: SE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2013-001318-14 | Sponsor Protocol Number: PHT-01-13 | Start Date*: 2013-07-15 | |||||||||||
Sponsor Name:PH&T SpA | |||||||||||||
Full Title: MULTICENTER, RANDOMIZED, DOUBLE BLIND, CONTROLLED, CLINICAL STUDY TO DEMONSTRATE THE THERAPEUTIC CLINICAL EQUIVALENCE OF TWO MOMETASONE NASAL SPRAYS IN THE RELIEF OF THE SIGNS AND SYMPTOMS OF SEASO... | |||||||||||||
Medical condition: SEASONAL ALLERGIC RHINITIS | |||||||||||||
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Population Age: Adolescents, Under 18, Adults | Gender: Male, Female | ||||||||||||
Trial protocol: BG (Completed) | |||||||||||||
Trial results: (No results available) |
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