- Trials with a EudraCT protocol (354)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (13)
354 result(s) found for: Allergic asthma.
Displaying page 1 of 18.
EudraCT Number: 2020-000883-42 | Sponsor Protocol Number: APHP180614 | Start Date*: 2021-01-18 | |||||||||||
Sponsor Name:ASSISTANCE PUBLIQUE - HOPITAUX DE PARIS | |||||||||||||
Full Title: Impact of omalizumab withdrawal after a 3 year duration treatment in well controlled severe allergic asthma : a multicentric randomized controlled trial | |||||||||||||
Medical condition: well controlled severe allergic asthma | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2009-011975-60 | Sponsor Protocol Number: AC-060A202 | Start Date*: 2010-09-30 | |||||||||||
Sponsor Name:Actelion Pharmaceuticals Ltd. | |||||||||||||
Full Title: A multi-center, double-blind, placebo-controlled, parallel-group study to establish proof-of-concept and explore the efficacy of different doses of ACT-129968 in adult patients with partly contro... | |||||||||||||
Medical condition: Allergic asthma | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: SE (Completed) DE (Completed) HU (Completed) PL (Completed) BG (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2007-001029-84 | Sponsor Protocol Number: AL0702rB | Start Date*: 2007-08-30 | ||||||||||||||||
Sponsor Name:Allergopharma Joachim Ganzer KG | ||||||||||||||||||
Full Title: A multicentre randomised, placebo-controlled, double-blind pivotal clinical trial for the evaluation of safety and efficacy of specific of immunotherapy with an aluminium hydroxide-adsorbed hypoall... | ||||||||||||||||||
Medical condition: ICD classification code: J45.0 and J30.1 | ||||||||||||||||||
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Population Age: Adults | Gender: Male, Female | |||||||||||||||||
Trial protocol: DE (Completed) SE (Completed) FI (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2008-006927-29 | Sponsor Protocol Number: CYT003-QbG10 11 | Start Date*: 2009-04-02 | |||||||||||
Sponsor Name:Cytos Biotechnology AG | |||||||||||||
Full Title: A Double-blind, Placebo-controlled Study to Assess Pharmacodynamic and Clinical Efficacy of CYT003-QbG10 in Patients with Persistent Allergic Asthma Bronchiale | |||||||||||||
Medical condition: Adult Patients with Persistent Allergic Asthma | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2015-002555-10 | Sponsor Protocol Number: ORCA2015 | Start Date*: 2015-11-19 | ||||||||||||||||||||||||||||||||||||
Sponsor Name:Imperial College | ||||||||||||||||||||||||||||||||||||||
Full Title: Effect of the CRTH2 antagonist OC459 on the response to rhinovirus challenge in asthma | ||||||||||||||||||||||||||||||||||||||
Medical condition: Asthma | ||||||||||||||||||||||||||||||||||||||
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Population Age: Adults | Gender: Male, Female | |||||||||||||||||||||||||||||||||||||
Trial protocol: GB (Completed) | ||||||||||||||||||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2015-001093-17 | Sponsor Protocol Number: 2015RC04 | Start Date*: 2016-04-22 | ||||||||||||||||
Sponsor Name:Tayside Medical Sciences Centre on behalf of University of Dundee & NHS Tayside | ||||||||||||||||||
Full Title: Proof of concept study to assess downstream effects of using combined intranasal fluticasone propionate plus azelastine nasal spray on asthmatic inflammation in patients with persistent asthma and ... | ||||||||||||||||||
Medical condition: Asthma and allergic rhinitis | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: GB (Prematurely Ended) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2012-005678-76 | Sponsor Protocol Number: AIFANumberFARM94793N | Start Date*: 2013-08-30 | |||||||||||
Sponsor Name:ALLEGRIA onlus | |||||||||||||
Full Title: Twenty-four month, multicenter, prospective, randomized, double-blind, placebo controlled, parallel-group study to evaluate the efficacy, safety, tolerability, and cost-effectiveness of allergen sp... | |||||||||||||
Medical condition: Allergic asthma to house dust mites | |||||||||||||
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Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2013-004920-12 | Sponsor Protocol Number: PRO-2013 | Start Date*: 2014-02-12 | |||||||||||||||||||||
Sponsor Name:LETI Pharma GmbH | |||||||||||||||||||||||
Full Title: Non-interventional Study in Allergic Patients Suffering from Grass Pollen Induced Rhinitis/Rhinoconjunctivitis with or without Asthma. Retrospective Assessment of the Efficacy of a Perennial Speci... | |||||||||||||||||||||||
Medical condition: Allergic rhinitis/rhinoconjunctivitis with or without concomitant asthma due to grass pollen allergy | |||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: CZ (Completed) | |||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2012-003698-25 | Sponsor Protocol Number: RHMMED1063 | Start Date*: 2013-02-26 | |||||||||||
Sponsor Name:University Hospital Southampton NHS Foundation Trust | |||||||||||||
Full Title: Proof of concept clinical trial examining the effect of clopidogrel on allergen challenge in asthma | |||||||||||||
Medical condition: asthma | |||||||||||||
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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: 2007-000097-23 | Sponsor Protocol Number: SAM109352 | Start Date*: 2007-09-04 | |||||||||||
Sponsor Name:GlaxoSmithKline | |||||||||||||
Full Title: Rationale for therapy with low dose steroids combined with long-acting beta2-agonists in patients with allergic asthma: redirecting innate immune responses by long-term treatment with high doses of... | |||||||||||||
Medical condition: Asthma | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2007-002808-18 | Sponsor Protocol Number: AL0701rP | Start Date*: 2007-10-31 | ||||||||||||||||
Sponsor Name:ALLERGOPHARMA JOACHIM GANZER KG | ||||||||||||||||||
Full Title: A double-blind placebo controlled dose-response study for evaluation of safety and efficacy of immunotherapy with a cocktail of recombinant major allergens of Timothy Grass Pollen (Phleum pratense)... | ||||||||||||||||||
Medical condition: ICD classification code: J45.0 and J30.1 | ||||||||||||||||||
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Population Age: Adults | Gender: Male, Female | |||||||||||||||||
Trial protocol: DE (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2006-000602-23 | Sponsor Protocol Number: 101-PG-COM-144 | Start Date*: 2007-09-17 | |||||||||||
Sponsor Name:Laboratorios LETI S.L. | |||||||||||||
Full Title: A randomized double blind, placebo controlled study to evaluate the efficacy and security of immunotherapy with a depigmented and polymerized allergen extract of Dermatophagoides pteronyssinus in p... | |||||||||||||
Medical condition: Mild to moderate asthma caused by sensitization againts dust mite Dermatophagoides Pteronyssinus. | |||||||||||||
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Population Age: Adolescents, Under 18, Adults | Gender: Male, Female | ||||||||||||
Trial protocol: PT (Not Authorised) | |||||||||||||
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 | ||||||||||||||||||
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Population Age: Adults | Gender: Male, Female | |||||||||||||||||
Trial protocol: SE (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2006-004191-13 | Sponsor Protocol Number: AVT-01/2/AST/04 | Start Date*: 2007-01-23 | |||||||||||
Sponsor Name:Avontec GmbH | |||||||||||||
Full Title: Efficacy and safety of AVT-01 10 mg single dose in patients with mild asthma challenged with inhaled tumor necrosis factor alpha – A double-blind, randomized, placebo-controlled clinical study | |||||||||||||
Medical condition: Male outpatients aged 18 - 65 with moderate persistent atopic asthma | |||||||||||||
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Population Age: Adults | Gender: Male | ||||||||||||
Trial protocol: GB (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2008-005205-19 | Sponsor Protocol Number: LPA112356 | Start Date*: 2009-01-27 | |||||||||||
Sponsor Name:GlaxoSmithKline Research & Development Limited | |||||||||||||
Full Title: A randomised, double-blind, placebo-controlled, 3-period cross-over study to evaluate the effect of two doses of GSK2190915 on the allergen-induced early asthmatic response in subjects with mild as... | |||||||||||||
Medical condition: Mild asthma | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2011-000762-35 | Sponsor Protocol Number: ID_2882 | Start Date*: 2011-11-18 | |||||||||||
Sponsor Name:A.O. UNIVERSITARIA INTEGRATA DI VERONA | |||||||||||||
Full Title: EFFECTS OF THE VITAMIN D ADMINISTRATION ON RESPIRATORY FUNCTIONS IN PAEDIATRIC PATIENTS SUFFERING FROM EFFORT ASTHMA | |||||||||||||
Medical condition: paediatric patients suffering from effort asthma | |||||||||||||
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Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2006-004187-32 | Sponsor Protocol Number: AVT-01/2/AST/02 | Start Date*: 2007-01-23 | |||||||||||
Sponsor Name:Avontec GmbH | |||||||||||||
Full Title: Efficacy and safety of AVT-01 5 mg once daily over 7 days in patients with moderate persistent atopic asthma – A double-blind, randomized, placebo-controlled clinical study | |||||||||||||
Medical condition: Male outpatients aged 18 - 65 with moderate persistent atopic asthma | |||||||||||||
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Population Age: Adults | Gender: Male | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2006-004190-94 | Sponsor Protocol Number: AVT-01/2/AST/03 | Start Date*: 2007-01-23 | |||||||||||
Sponsor Name:Avontec GmbH | |||||||||||||
Full Title: Efficacy and safety of AVT-01 10 mg once daily over 7 days in patients with moderate persistent atopic asthma – A double-blind, randomized, placebo-controlled clinical study | |||||||||||||
Medical condition: Male outpatients aged 18 - 65 with moderate persistent atopic asthma | |||||||||||||
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Population Age: Adults | Gender: Male | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2013-001953-28 | Sponsor Protocol Number: 2012RC15 | Start Date*: 2013-08-20 | |||||||||||
Sponsor Name:Tayside Medical Sciences Centre on behalf of University of Dundee & NHS Tayside | |||||||||||||
Full Title: Proof of concept study to evaluate single and chronic dosing effects of ultra-long acting bronchodilator therapy on mannitol challenge in asthmatic patients taking inhaled corticosteroids | |||||||||||||
Medical condition: Asthma | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2014-005317-23 | Sponsor Protocol Number: 2013RC06 | Start Date*: 2015-11-16 | |||||||||||
Sponsor Name:Tayside Medical Sciences Centre on behalf of University of Dundee & NHS Tayside | |||||||||||||
Full Title: Effects of ultra-long acting bronchodilator therapy assessed by impulse oscillometry in smoking asthmatics taking inhaled corticosteroids | |||||||||||||
Medical condition: Asthma | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
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