- Trials with a EudraCT protocol (219)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
219 result(s) found for: Atopy.
Displaying page 1 of 11.
EudraCT Number: 2009-015679-28 | Sponsor Protocol Number: RHM CHI0499 | Start Date*: 2010-09-29 | |||||||||||
Sponsor Name:Southampton University Hospitals Trust | |||||||||||||
Full Title: PRIMARY PREVENTION OF ATOPY AND ASTHMA WITH ALLERGEN SUBLINGUAL IMMUNOTHERAPY | |||||||||||||
Medical condition: Development of atopy | |||||||||||||
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Population Age: Infants and toddlers, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2009-012194-35 | Sponsor Protocol Number: 290404BS | Start Date*: 2009-12-22 |
Sponsor Name:bioskin GmbH | ||
Full Title: A single-center, randomized, controlled, observer-blind, phase IV study to develop the atopic localized eczema regression test (ALERT) using marketed topical corticosteroid formulations of differen... | ||
Medical condition: Patients with a pre-disposition for Atopic Dermatitis | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: DE (Completed) | ||
Trial results: View results |
EudraCT Number: 2006-007096-32 | Sponsor Protocol Number: PREV1234 | Start Date*: 2009-01-07 |
Sponsor Name:Medizinische Universität Wien, Univ. Kinderklinik | ||
Full Title: Prevention od new sensitization by sublingual immunotherapy in children 2-4 years of age with allergic mono-sensitization | ||
Medical condition: Children (2-4years of age) from atopy prone families with an allergic sensitization as defined by positive skin prick test or positive allergen-specific IgE to grass pollen or house dust mite aller... | ||
Disease: | ||
Population Age: Children, Under 18 | Gender: Male, Female | |
Trial protocol: AT (Completed) | ||
Trial results: View results |
EudraCT Number: 2009-017407-28 | Sponsor Protocol Number: H 527 000-0917 | Start Date*: 2010-01-27 | |||||||||||
Sponsor Name:Almirall Hermal GmbH | |||||||||||||
Full Title: A phase II, single-center, randomized, controlled, double-blind study to assess effects on skin conditions and patient reported outcome of a topical formulation containing LAS41002 on lesional skin... | |||||||||||||
Medical condition: Clinical condition of atopic eczema mild to moderate defined by a local SCORAD of at least 5 with • erythma ≥ 2 • lichenification ≥ 1 • dryness ≥ 1 • itching ≥ 1 • Erlangen atopy score sum equal... | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2008-007323-64 | Sponsor Protocol Number: P441201CD | Start Date*: 2009-02-09 | |||||||||||
Sponsor Name:Serentis Limited | |||||||||||||
Full Title: A phase II, double-blind, vehicle controlled study to determine the efficacy, safety and toleration of SRD441 ointment in patients with atopic dermatitis | |||||||||||||
Medical condition: Atopic Dermatitis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) FI (Completed) BG (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2005-005523-34 | Sponsor Protocol Number: NAI002/I | Start Date*: 2006-04-11 |
Sponsor Name:University of Dundee (Research & Innovation Services) | ||
Full Title: A PROOF OF CONCEPT STUDY TO EVALAUTE EFFECTS INTRANASAL SALMETEROL AND FLUTICASONE GIVEN ALONE AND IN COMBINATION IN ALLERGIC RHINITIS | ||
Medical condition: Allergic Rhinitis | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: GB (Prematurely Ended) | ||
Trial results: View results |
EudraCT Number: 2006-001611-30 | Sponsor Protocol Number: AJAE1001 | Start Date*: 2006-08-22 |
Sponsor Name:Hammersmith Hospital NHS Trust | ||
Full Title: Clinical trial comparing the effect of Acetaminophen and Ibuprofen on the duration of influenza viral shedding in young children (Pilot study) | ||
Medical condition: Influenza in children [positive rapid diagnostic test (QuickVue influenza test)confirmed by influenza PCR] Infants and young children shed the influenza virus for longer periods than adults, durat... | ||
Disease: | ||
Population Age: Infants and toddlers, Children, Under 18 | Gender: Male, Female | |
Trial protocol: GB (GB - no longer in EU/EEA) | ||
Trial results: View results |
EudraCT Number: 2007-004876-38 | Sponsor Protocol Number: 603-PG-PSC-165 | Start Date*: 2007-12-10 | |||||||||||
Sponsor Name:LETI Pharma GmbH | |||||||||||||
Full Title: An open label multicenter phase 2 study for the initial evaluation of the tolerability of Birch pollen extract in patients suffering from atopic eczema and clinical relevant IgE-mediated sensitizat... | |||||||||||||
Medical condition: Atopic eczema and clinical relevant IgE-mediated sensitisation against birch pollen | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2006-003066-34 | Sponsor Protocol Number: 101-PG-PSC-150 | Start Date*: 2007-01-23 | |||||||||||
Sponsor Name:LETI Pharma GmbH | |||||||||||||
Full Title: A randomized, double blinded, placebo controlled multicenter study for the efficacy and safety of Depigoid® House dust mites (HDM) in patients suf-fering from moderate to severe atopic eczema. | |||||||||||||
Medical condition: Moderate to severe atopic eczema with or without rhinitis and/or rhinoconjunctivitis caused by clinical relevant IgE-mediated sensitization against House dust mites (HDM) leading to aggravation of ... | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2009-013429-40 | Sponsor Protocol Number: CVAK694A2205 | Start Date*: 2009-10-15 | |||||||||||
Sponsor Name:Novartis Pharma Services AG | |||||||||||||
Full Title: Randomized, double-blind, placebo-controlled trial to determine the capacity of VAK694 to elicit long term immune tolerance when combined with subcutaneous allergen immunotherapy for the treatment ... | |||||||||||||
Medical condition: Seasonal allergic rhinitis | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2021-006903-14 | Sponsor Protocol Number: ARQ-151-315 | Start Date*: Information not available in EudraCT | |||||||||||
Sponsor Name:Arcutis Biotherapeutics, Inc. | |||||||||||||
Full Title: A Phase 3, 4-Week, Parallel Group, Double Blind, Vehicle-Controlled Study of the Safety and Efficacy of ARQ-151 Cream 0.05% Administered QD in Subjects with Atopic Dermatitis | |||||||||||||
Medical condition: Atopic Dermatitis | |||||||||||||
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Population Age: Children, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: PL (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2004-004443-22 | Sponsor Protocol Number: Spirig I 04-05 | Start Date*: Information not available in EudraCT | |||||||||||
Sponsor Name:Spirig Pharma AG | |||||||||||||
Full Title: Untersuchung der Wirksamkeit einer glycerinhaltigen Creme bei der Behandlung von Atopischer Dermatitis. Kontrolliert, randomisierte Doppel-Blind-Studie. | |||||||||||||
Medical condition: Atopic Dermatitis | |||||||||||||
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Population Age: Adolescents, Under 18, Adults | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2012-002106-48 | Sponsor Protocol Number: BCF-2009.01 | Start Date*: 2012-07-06 |
Sponsor Name:University College Dublin | ||
Full Title: An Investigative Study to characterize gene expression patterns in myeloid cells that are triggered during acute asthma exacerbations, and to identify associated genes/gene networks that are Omaliz... | ||
Medical condition: Asthma | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: IE (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2017-001765-25 | Sponsor Protocol Number: CASM981CUS09 | Start Date*: 2017-09-28 |
Sponsor Name:Novartis | ||
Full Title: An Investigation of the Safety and Efficacy of Elidel® 1% Cream in Atopic Disease Modification, Assessed in a 3-year Randomized Doubleblind Vehicle Controlled Phase to Evaluate Effects on Atopic De... | ||
Medical condition: Atopic Dermatitis | ||
Disease: | ||
Population Age: Infants and toddlers, Under 18 | Gender: Male, Female | |
Trial protocol: Outside EU/EEA | ||
Trial results: View results |
EudraCT Number: 2007-003194-82 | Sponsor Protocol Number: VAI03 | Start Date*: 2007-09-05 | |||||||||||
Sponsor Name:University of Dundee | |||||||||||||
Full Title: A proof of concept study to evaluate differential tachyphylaxis of α1 and α2 adrenoreceptor mediated decongestant response to oxymetazoline and its acute reversal by corticosteroid in healthy volun... | |||||||||||||
Medical condition: This is a proof of concept trial on Healthy Volunteers to evaluate the tolerance of nasal adrenoreceptors to prolonged decongestant use and upregulation by intranasal steroids. The medical conditio... | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2010-020407-73 | Sponsor Protocol Number: D9830C00008 | Start Date*: 2010-10-27 |
Sponsor Name:AstraZeneca AB | ||
Full Title: A double-blind, placebo-controlled, randomised, parallel-group, phase-II, multi-centre study to assess the efficacy, safety and tolerability of 4 twice daily doses and 2 once daily doses of AZD1981... | ||
Medical condition: asthma | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: SK (Completed) | ||
Trial results: View results |
EudraCT Number: 2007-003291-19 | Sponsor Protocol Number: VAI01 | Start Date*: 2009-07-30 | ||||||||||||||||
Sponsor Name:University of Dundee | ||||||||||||||||||
Full Title: A proof of concept study to evaluate if concomitant topical intranasal steroid prevents tolerance and rebound congestion due to regular oxymetazoline in persistent allergic rhinitis | ||||||||||||||||||
Medical condition: Allergic Rhinitis | ||||||||||||||||||
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Population Age: Adults | Gender: Male, Female | |||||||||||||||||
Trial protocol: GB (Prematurely Ended) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2006-006469-17 | Sponsor Protocol Number: 2006-001 | Start Date*: Information not available in EudraCT |
Sponsor Name:St Olavs Hospital, University Hospital of Trondheim [...] | ||
Full Title: A multicenter study to investigate the Sensitivity and Specificity of Aridol (Mannitol)Challenge as compared with Methacholine Challenge to predict a diagnosis of Asthma by a Specialist Pulmonologi... | ||
Medical condition: The detection of bronchial hyperresponsiveness in patients with suspected asthma | ||
Disease: | ||
Population Age: Adolescents, Under 18, Adults | Gender: Male, Female | |
Trial protocol: NO (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2008-004432-20 | Sponsor Protocol Number: ACE-ATOPI-1 | Start Date*: 2008-09-03 | |||||||||||
Sponsor Name:ACE Aps | |||||||||||||
Full Title: Efficacy and tolerability of captopril oinment 0,1% og 0,3% in atopic dermatitis. A randomised, double-blind, placebocontrolled, doseescalating, intra-individual clinical study. | |||||||||||||
Medical condition: Atopic Dermatitis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2004-002926-23 | Sponsor Protocol Number: RV2478B 03 LT 301 100 MVC | Start Date*: 2004-12-22 | |||||||||||
Sponsor Name:INSTITUT DE RECHERCHE PIERRE FABRE | |||||||||||||
Full Title: Evaluation of the impact of the moisturizing milk RV2478B on the use of corticoids and on quality of life, in a population of children with atopic dermatitis. | |||||||||||||
Medical condition: Atopic dermatitis | |||||||||||||
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Population Age: Newborns, Infants and toddlers, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: (No results available) |
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