- Trials with a EudraCT protocol (76)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (85)
76 result(s) found for: Perennial Allergic Rhinitis.
Displaying page 2 of 4.
EudraCT Number: 2007-006562-15 | Sponsor Protocol Number: FFU111439 | Start Date*: 2008-03-28 | |||||||||||
Sponsor Name:GlaxoSmithKline Research & Development Ltd | |||||||||||||
Full Title: A Randomized, Double-Blind, Placebo-Controlled, Parallel-Group, Multicenter Study to Evaluate the Efficacy and Safety of Once-Daily Intranasal Administration of Fluticasone Furoate Nasal Spray 110m... | |||||||||||||
Medical condition: Perennial Allergic Rhinitis (PAR) in adults and children of 12 years and older. | |||||||||||||
|
|||||||||||||
Population Age: Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: EE (Completed) HU (Completed) SK (Completed) DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2018-003715-22 | Sponsor Protocol Number: DMV01-SIT-015 | Start Date*: 2020-11-04 | ||||||||||||||||||||||||||
Sponsor Name:Inmunotek, S.L. | ||||||||||||||||||||||||||||
Full Title: Prospective, randomized, placebo-controlled, multi-center trial comparing the efficacy and safety of subcutaneous immunotherapy with a mixture of grasses and mites at adequate doses versus monother... | ||||||||||||||||||||||||||||
Medical condition: Mild to moderate asthma and allergic rhinitis / rhinoconjunctivitis (intermittent or persistent) due to hypersensitivity to house dust mites (Dermatophagoides pteronyssinus and / or D. farinae) and... | ||||||||||||||||||||||||||||
|
||||||||||||||||||||||||||||
Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||
Trial protocol: ES (Prematurely Ended) | ||||||||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2008-006258-16 | Sponsor Protocol Number: AL0801rB | Start Date*: 2008-11-19 | ||||||||||||||||
Sponsor Name:ALLERGOPHARMA JOACHIM GANZER KG | ||||||||||||||||||
Full Title: A multicentre randomised placebo-controlled double-blind clinical trial for the immunological and histological evaluation of specific immunotherapy with an aluminium hydroxide-adsorbed recombinant ... | ||||||||||||||||||
Medical condition: ICD classification code: J45.0 and J30.1 | ||||||||||||||||||
|
||||||||||||||||||
Population Age: Adults | Gender: Male, Female | |||||||||||||||||
Trial protocol: SE (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2005-005449-20 | Sponsor Protocol Number: P04683 | Start Date*: 2006-08-30 | |||||||||||
Sponsor Name:Schering-Plough Research Institute | |||||||||||||
Full Title: Double-Blind, Randomized, Placebo-Controlled, Parallel-Groups, Multicenter/ Multinational, Efficacy and Safety Study of Desloratadine 5 mg in the Treatment of Subjects With Allergic Rhinitis who Me... | |||||||||||||
Medical condition: Intermittent Allergic Rhinitis (Allergic Rhinitis) | |||||||||||||
|
|||||||||||||
Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FI (Completed) PT (Completed) ES (Completed) DE (Completed) HU (Completed) SE (Completed) GR (Completed) DK (Completed) IT (Completed) BE (Completed) Outside EU/EEA | |||||||||||||
Trial results: View results |
EudraCT Number: 2009-011827-30 | Sponsor Protocol Number: EMC-ALGO-SCIT-2009/1 | Start Date*: 2009-08-14 | ||||||||||||||||
Sponsor Name:ErasmusMC-University Medical Center Rotterdam | ||||||||||||||||||
Full Title: Cost-effectiveness of subcutaneous immunotherapy in adults with allergic rhinitis. | ||||||||||||||||||
Medical condition: Allergic rhinitis. | ||||||||||||||||||
|
||||||||||||||||||
Population Age: Adults | Gender: Male, Female | |||||||||||||||||
Trial protocol: NL (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2013-004669-15 | Sponsor Protocol Number: CP007A | Start Date*: 2014-06-16 | |||||||||||
Sponsor Name:Circassia Limited | |||||||||||||
Full Title: An Optional Prospective Follow-on Study to Evaluate the Continued Efficacy and Safety of Cat-PAD in Cat Allergic Subjects up to Five Years after the Administration of Treatment | |||||||||||||
Medical condition: Treatment of cat allergen induced rhinoconjunctivitis in patients with clinically relevant symptoms | |||||||||||||
|
|||||||||||||
Population Age: Adolescents, Under 18, Adults | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Completed) DE (Prematurely Ended) CZ (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2014-004921-41 | Sponsor Protocol Number: P06332 | Start Date*: 2015-02-24 |
Sponsor Name:Corporation Schering-Plough K.K. | ||
Full Title: Multicenter, double-blind, randomized, placebo-controlled study of mometasone furoate nasal spray in pediatric subjects with perennial allergic rhinitis | ||
Medical condition: perennial allergic rhinitis | ||
Disease: | ||
Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | |
Trial protocol: Outside EU/EEA | ||
Trial results: View results |
EudraCT Number: 2010-020079-22 | Sponsor Protocol Number: DG40.08 | Start Date*: Information not available in EudraCT | |||||||||||
Sponsor Name:STALLERGENES S.A. | |||||||||||||
Full Title: Determination of sensitivity and specificity of five solutions of allergen extract (5 grasses, birch, ragweed pollens and Dermatophagoides pteronyssinus and Dermatophagoides farinae mites) for diag... | |||||||||||||
Medical condition: Allergy to grass pollen Allergy to birch pollen Allergy to ragweed pollen Allergy to mites | |||||||||||||
|
|||||||||||||
Population Age: Children, Adolescents, Under 18, Adults | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2004-004749-17 | Sponsor Protocol Number: FFR101747 | Start Date*: 2005-03-22 |
Sponsor Name:GlaxoSmithKline Research & Development Ltd | ||
Full Title: A randomized, double-blind, placebo-controlled, 2-week crossover, knemometric assessment of the effect of once daily GW685698X Aqueous Nasal Spray 100 mcg on short term growth in children ages 6 - ... | ||
Medical condition: Seasonal and/or perennial allergic rhinitis | ||
Disease: | ||
Population Age: Children, Under 18 | Gender: Male, Female | |
Trial protocol: DK (Completed) | ||
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 | |||||||||||||
|
|||||||||||||
Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2007-003572-19 | Sponsor Protocol Number: V00114 CP 302 2A | Start Date*: 2007-12-04 |
Sponsor Name:Pierre Fabre Médicament | ||
Full Title: EFFICACY AND SAFETY STUDY OF THE ANTIHISTAMINE V0114CP 2.5MG IN THE TREATMENT OF PERENNIAL ALLERGIC RHINITIS. RANDOMISED, DOUBLE-BLIND, THREE ARM PARALLEL GROUP STUDY INCLUDING PLACEBO AND ACTIV... | ||
Medical condition: The intended indication for the product under development is the treatment of perennial allergic rhinitis. | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: EE (Prematurely Ended) LT (Prematurely Ended) CZ (Completed) GB (Prematurely Ended) ES (Completed) FI (Prematurely Ended) LV (Completed) AT (Prematurely Ended) | ||
Trial results: View results |
EudraCT Number: 2008-005939-15 | Sponsor Protocol Number: DC04/RUP/3/08 | Start Date*: 2009-02-11 | ||||||||||||||||
Sponsor Name:J. Uriach y Compañía, S.A. | ||||||||||||||||||
Full Title: Efficacy and safety of rupatadine in persistent allergic rhinitis and health-related quality of life in children age 6-11 years: A randomized, double blind, placebo-controlled clinical trial. | ||||||||||||||||||
Medical condition: Persistent Allergic Rhinitis | ||||||||||||||||||
|
||||||||||||||||||
Population Age: Children, Under 18 | Gender: Male, Female | |||||||||||||||||
Trial protocol: HU (Completed) ES (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2011-000674-58 | Sponsor Protocol Number: AL1011av | Start Date*: 2011-07-28 | ||||||||||||||||
Sponsor Name:Allergopharma Joachim Ganzer KG | ||||||||||||||||||
Full Title: Double-blind, placebo controlled study to investigate the dose response of an allergoid preparation of Phleum pratense in adult patients with IgE mediated allergic Rhinitis / Rhinoconjunctivitis wi... | ||||||||||||||||||
Medical condition: ICD classification code: J 45.0 and J 30.1 | ||||||||||||||||||
|
||||||||||||||||||
Population Age: Adults | Gender: Male, Female | |||||||||||||||||
Trial protocol: DE (Completed) | ||||||||||||||||||
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 | |||||||||||||
|
|||||||||||||
Population Age: Children, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: PL (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2017-000893-12 | Sponsor Protocol Number: 8302 | Start Date*: 2017-08-31 | |||||||||||||||||||||
Sponsor Name:The Newcastle Upon Tyne Hospitals NHS Foundation Trust | |||||||||||||||||||||||
Full Title: Nasal Airway Obstruction Study | |||||||||||||||||||||||
Medical condition: Deviated Nasal Septum | |||||||||||||||||||||||
|
|||||||||||||||||||||||
Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) | |||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2008-008448-26 | Sponsor Protocol Number: 603-PG-PSC-173 | Start Date*: 2009-10-20 | ||||||||||||||||
Sponsor Name:LETI Pharma GmbH | ||||||||||||||||||
Full Title: Randomized, double-blind, parallel group, multicenter study to evaluate the efficacy and safety of four doses of depigmented glutaraldehyde polymerized birch pollen allergenic extract (Depigoid® Bi... | ||||||||||||||||||
Medical condition: Allergic rhinitis and/or rhinoconjunctivitis, with or without intermittent asthma, caused by birch pollen. | ||||||||||||||||||
|
||||||||||||||||||
Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: DE (Completed) LT (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 | |||||||||||||
|
|||||||||||||
Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2007-000823-16 | Sponsor Protocol Number: AL0703st | Start Date*: 2007-11-20 | |||||||||||
Sponsor Name:Allergopharma Joachim Ganzer KG | |||||||||||||
Full Title: A multicenter, multinational, placebo-controlled, double-blind, randomized study to evaluate efficacy and safety of a perennial, sublingual specific immunotherapy in patielnts with rhinoconjunctivi... | |||||||||||||
Medical condition: IgE-mediated allergic disease manifested as symptoms of allergic rhinoconjunctivitis with or without controlled asthma caused by grass pollen. | |||||||||||||
|
|||||||||||||
Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) IT (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 | |||||||||||||
|
|||||||||||||
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: 2009-011504-36 | Sponsor Protocol Number: AL0906rP | Start Date*: 2010-02-02 | ||||||||||||||||
Sponsor Name:Allergopharma Joachim Ganzer KG | ||||||||||||||||||
Full Title: Randomised double blind placebo controlled pivotal study to evaluate efficacy and safety of rPhleum in adult and adolescent patients suffering from rhinoconjunctivitis +/- controlled Asthma | ||||||||||||||||||
Medical condition: ICD classification code: J45.0 and J 30.1 Rhiniconjunctivitis +/- asthma bronchiale | ||||||||||||||||||
|
||||||||||||||||||
Population Age: Adolescents, Under 18, Adults | Gender: Male, Female | |||||||||||||||||
Trial protocol: DE (Completed) GB (Completed) PL (Completed) FR (Completed) ES (Completed) | ||||||||||||||||||
Trial results: View results |
Subscribe to this Search
To subscribe to the RSS feed for this search click here
.
This will provide an RSS feed for clinical trials matching your search that have been added or updated in the last 7 days.
To subscribe to the RSS feed for this search click here

Download Options: | |
---|---|
Number of Trials to download: | |
Download Content: | |
Download Format: | |
Note, where multi-state trials are shown in search results, selecting "Full Trial details" will download full information for each of the member states/countries involved in the trial. |
