- Trials with a EudraCT protocol (156)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (51)
156 result(s) found for: Allergic conjunctivitis.
Displaying page 1 of 8.
EudraCT Number: 2017-003953-41 | Sponsor Protocol Number: C-09-50 | Start Date*: 2017-11-22 | |||||||||||
Sponsor Name:Alcon Research Ltd | |||||||||||||
Full Title: An Open-label, Long-term Study, with AL-4943A Ophthalmic Solution, 0.2% in Patients with Allergic Conjunctivitis | |||||||||||||
Medical condition: Allergic conjunctivitis | |||||||||||||
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Population Age: Adolescents, Under 18, Adults | Gender: Male, Female | ||||||||||||
Trial protocol: Outside EU/EEA | |||||||||||||
Trial results: View results |
EudraCT Number: 2017-003841-39 | Sponsor Protocol Number: JPN-P-2010-1 | Start Date*: 2017-11-07 | |||||||||||
Sponsor Name:Alcon Research | |||||||||||||
Full Title: Clinical Evaluation of 0.1% Olopatadine Hydrochloride Ophthalmic Solution in Paediatric Patients | |||||||||||||
Medical condition: allergic conjunctivitis | |||||||||||||
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Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: Outside EU/EEA | |||||||||||||
Trial results: View results |
EudraCT Number: 2007-000209-31 | Sponsor Protocol Number: LACTO2 | Start Date*: 2007-03-08 | |||||||||||
Sponsor Name:UNIVERSITA CAMPUS BIOMEDICO | |||||||||||||
Full Title: Efficacy of Lactobacillus Rhamnosus GG on preventing acute phases in patients affected by allergic conjunctivitis | |||||||||||||
Medical condition: allergic conjunctivitis | |||||||||||||
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Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2017-002728-26 | Sponsor Protocol Number: C-12-028 | Start Date*: 2017-11-07 | |||||||||||
Sponsor Name:Alcon Research | |||||||||||||
Full Title: A Multicenter, Randomized, Double-Masked, Vehicle-Controlled, Parallel-Group Study Evaluating the Safety of olopatadine hydrochloride (AL-4943A) Ophthalmic Solution 0.77% Administered Once Daily | |||||||||||||
Medical condition: asymptomatic allergic conjunctivitis | |||||||||||||
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Population Age: Children, Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: Outside EU/EEA | |||||||||||||
Trial results: View results |
EudraCT Number: 2005-003460-35 | Sponsor Protocol Number: E03/05/PP-M | Start Date*: 2005-10-27 | |||||||||||
Sponsor Name:ALK-Abelló, S.A. | |||||||||||||
Full Title: Evaluación de los cambios inmunológicos tras la inmunoterapia subcutánea con un extracto de Phleum pratense | |||||||||||||
Medical condition: Rhinoconjunctivitis | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2012-005227-33 | Sponsor Protocol Number: PILIT_2013 | Start Date*: 2013-03-22 | ||||||||||||||||
Sponsor Name:Department of Respiratory Diseases, Aarhus University Hospital | ||||||||||||||||||
Full Title: Effect of Intralymphatic Immunotherapy on Basophil Response and Plasma Cell Kinetics in Allergic Patients | ||||||||||||||||||
Medical condition: allergic rhino-conjunctivitis | ||||||||||||||||||
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Population Age: Adults | Gender: Male, Female | |||||||||||||||||
Trial protocol: DK (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2016-004317-27 | Sponsor Protocol Number: EXC458-C001/C-12-010 | Start Date*: 2017-07-03 | |||||||||||
Sponsor Name:Alcon China Ophthalmic | |||||||||||||
Full Title: A Comparative Study of Olopatadine Hydrochloride Ophthalmic Solution 0.2% QD vs Olopatadine Hydrochloride Ophthalmic Solution 0.1% BID in the Treatment of Allergic Conjunctivitis in Chinese Subjects | |||||||||||||
Medical condition: Allergic conjunctivitis | |||||||||||||
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Population Age: Children, Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: Outside EU/EEA | |||||||||||||
Trial results: View results |
EudraCT Number: 2007-004473-26 | Sponsor Protocol Number: LT0427-PII-01/07 | Start Date*: 2007-10-16 | |||||||||||
Sponsor Name:Laboratoires Théa | |||||||||||||
Full Title: Efficacy and safety of sodium cromolyn eye drops compared with placebo eye drops in patients with a history of allergic conjunctivitis using the Conjunctival Allergen Challenge model. | |||||||||||||
Medical condition: allergic conjunctivitis | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Ongoing) | |||||||||||||
Trial results: (No results available) |
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: 2017-001838-26 | Sponsor Protocol Number: THEA-LT0455-PIV-09/16 | Start Date*: 2017-07-26 | |||||||||||
Sponsor Name:THEA | |||||||||||||
Full Title: Comparison of NAABAK® efficacy versus FLUCON® in the treatment of moderate manifestations of allergic conjunctivitis to birch pollen in subjects exposed to birch in ALYATEC’s environmental exposure... | |||||||||||||
Medical condition: Subjects presenting moderate allergic conjunctivitis to birch pollen | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2005-002501-23 | Sponsor Protocol Number: V040.05 | Start Date*: 2005-12-12 | |||||||||||
Sponsor Name:Stallergenes S.A | |||||||||||||
Full Title: A randomised, double-blind, placebo-controlled, multi-national, multi-centre, phase III extension study to assess the long term efficacy, safety and carry-over effect of one dose of sublingual imm... | |||||||||||||
Medical condition: Grass Pollen Related Allergic Rhinoconjunctivitis | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) AT (Prematurely Ended) CZ (Completed) SK (Completed) ES (Completed) DK (Completed) IT (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2021-006533-19 | Sponsor Protocol Number: SC-312A | Start Date*: 2022-11-15 | ||||||||||||||||
Sponsor Name:ROXALL Medizin GmbH | ||||||||||||||||||
Full Title: Phase II-III study to assess the efficacy and safety of subcutaneous cluster-immunotherapy in patients suffering from grass pollen allergy | ||||||||||||||||||
Medical condition: Patients with grass pollen-related allergic rhinitis/rhinoconjunctivitis and well-controlled mild-to-moderate or without asthma | ||||||||||||||||||
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Population Age: Adults | Gender: Male, Female | |||||||||||||||||
Trial protocol: DE (Completed) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2008-006292-77 | Sponsor Protocol Number: SB/0027 | Start Date*: 2009-05-08 | ||||||||||||||||||||||||||
Sponsor Name:HAL Allergy | ||||||||||||||||||||||||||||
Full Title: SUBLIVAC® Birch PROBE study | ||||||||||||||||||||||||||||
Medical condition: IgE mediated allergic disorders triggered by birch pollen | ||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||
Trial protocol: DE (Completed) | ||||||||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2020-004372-17 | Sponsor Protocol Number: TT-06 | Start Date*: 2021-04-20 | ||||||||||||||||
Sponsor Name:ALK-Abelló A/S | ||||||||||||||||||
Full Title: Efficacy and safety of the SQ tree sublingual immunotherapy tablet in children and adolescents (5 through 17 years of age) with moderate to severe allergic rhinitis and/or conjunctivitis induced by... | ||||||||||||||||||
Medical condition: Tree pollen induced allergic rhinitis and/or conjuctivitis. | ||||||||||||||||||
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Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | |||||||||||||||||
Trial protocol: DE (Completed) LT (Completed) HU (Completed) SK (Completed) PL (Completed) AT (Completed) DK (Completed) BE (Completed) NL (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2005-004768-22 | Sponsor Protocol Number: C-05-30 | Start Date*: 2006-06-12 | |||||||||||
Sponsor Name:ALCON ITALIA | |||||||||||||
Full Title: Clinical study of the mast-cell stabilizing effects of the Olopatadine using the Conjunctival Allergen Challeenge model | |||||||||||||
Medical condition: subjects with a clinical history of seasonal allergic conjunctivitis, but asymptomatic and free of any topical or systemic medication at baseline | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2021-002881-42 | Sponsor Protocol Number: SL-351A | Start Date*: 2023-02-07 | ||||||||||||||||||||||||||
Sponsor Name:ROXALL Medizin GmbH | ||||||||||||||||||||||||||||
Full Title: Phase II study to assess the tolerability, safety and efficacy of sublingual immunotherapy in patients suffering from grass pollen allergy | ||||||||||||||||||||||||||||
Medical condition: Patients with grass pollen-related allergic rhinitis/rhino-conjunctivitis (with well-controlled mild-to-moderate or without asthma) | ||||||||||||||||||||||||||||
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Population Age: Adults | Gender: Male, Female | |||||||||||||||||||||||||||
Trial protocol: DE (Completed) | ||||||||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2004-001910-15 | Sponsor Protocol Number: V034.04 | Start Date*: 2004-11-22 | |||||||||||
Sponsor Name:Stallergenes S.A. | |||||||||||||
Full Title: Randomised, double-blind, placebo-controlled, multinational, multi-centre, Phase IIb / III study of the efficacy and safety of three doses of sublingual immunotherapy (SLIT) administered as tablets... | |||||||||||||
Medical condition: Grass Pollen Related Allergic Rhinoconjunctivitis | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: CZ (Completed) SK (Completed) HU (Completed) DE (Completed) AT (Completed) IT (Completed) ES (Completed) DK (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2006-005681-39 | Sponsor Protocol Number: FAR-0201 | Start Date*: 2007-01-22 | |||||||||||
Sponsor Name:FARMIGEA | |||||||||||||
Full Title: A RANDOMIZED, DOUBLE-BLIND, MULTICENTER PARALLEL GROUP STUDY ON EFFICACY AND SAFETY OF KETOTIFEN FUMARATE 0.05 OPHTHALMIC SOLUTION VERSUS KETOTIFEN FUMARATE 0.025 | |||||||||||||
Medical condition: Patients with seasonal allergic conjunctivitis and history of ocular allergies for at least 2 years. | |||||||||||||
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Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2007-000047-99 | Sponsor Protocol Number: MK-0476P2181V1 | Start Date*: 2007-03-06 | ||||||||||||||||||||||||||
Sponsor Name:Tari Haahtela | ||||||||||||||||||||||||||||
Full Title: Montelukast as a controller of atopic syndrome - MONTAS-study | ||||||||||||||||||||||||||||
Medical condition: Allergic symptoms (rhinitis, conjunctivits, asthma, oral symptoms and atopic eczema) caused by pollen allergy to birch or timothy. | ||||||||||||||||||||||||||||
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Population Age: Adults | Gender: Male, Female | |||||||||||||||||||||||||||
Trial protocol: FI (Completed) | ||||||||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2005-002502-34 | Sponsor Protocol Number: VO42.05 | Start Date*: 2005-12-05 | |||||||||||
Sponsor Name:Stallergenes S.A. | |||||||||||||
Full Title: A randomised, double-blind, placebo-controlled, multi-national, multi-centre, Phase III paediatric study of the efficacy and safety of one dose of sublingual immunotherapy (SLIT) administered as al... | |||||||||||||
Medical condition: Grass Pollen Related Allergic Rhinoconjunctivitis | |||||||||||||
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Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: EE (Prematurely Ended) DE (Completed) DK (Completed) LV (Completed) | |||||||||||||
Trial results: (No results available) |
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