- Trials with a EudraCT protocol (266)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (14)
266 result(s) found for: Atopic eczema.
Displaying page 1 of 14.
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: 2006-006982-17 | Sponsor Protocol Number: 05.09.2006 | Start Date*: 2007-07-12 | |||||||||||
Sponsor Name:Division of Special and Environmental Dermatology | |||||||||||||
Full Title: UVA 1 therapy versus 5-MOP UVA photochemotherapy for patients with severe generalized atopic dermatitis | |||||||||||||
Medical condition: Severe generalized atopic dermatitis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: AT (Completed) | |||||||||||||
Trial results: View results |
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: 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) |
EudraCT Number: 2008-003485-25 | Sponsor Protocol Number: V00034 CR 402 1B | Start Date*: 2008-10-01 | |||||||||||
Sponsor Name:Pierre Fabre Médicament | |||||||||||||
Full Title: Impact of the V0034CR 01B emollient on atopic dermatitis symptoms in children. A randomised, placebo-controlled, parallel-groups, double-blind study | |||||||||||||
Medical condition: Children between 2 and 7 years, presenting with atopic dermatitis according to the diagnostic criteria of the UK Working party and whose IGA score is < or = 1 at inclusion. | |||||||||||||
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Population Age: Children, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: LT (Completed) FR (Completed) EE (Completed) DE (Completed) PL (Completed) LV (Completed) IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2010-021284-33 | Sponsor Protocol Number: protocoltwo17.12.09. | Start Date*: 2010-10-07 | ||||||||||||||||||||||||||
Sponsor Name:Research and Development Department, John Radcliffe Hospital | ||||||||||||||||||||||||||||
Full Title: Proof of concept study of combined allergen immunotherapy and antibiotics for the treatment of chronic atopic eczema | ||||||||||||||||||||||||||||
Medical condition: Severe chronic atopic eczema | ||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||
Trial protocol: GB (Completed) | ||||||||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2009-011931-11 | Sponsor Protocol Number: H 552 000 - 0911 | Start Date*: Information not available in EudraCT | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Sponsor Name:Almirall Hermal GmbH | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Full Title: Explorative, double-blind, randomized, controlled multi-center phase II study to evaluate the efficacy and safety of topically applied combinational product LAS41003 once daily versus corresponding... | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Medical condition: Patients aged 18 and older suffering from at least one clinically diagnosed superinfected or impetiginised eczema such as e.g. • superinfected or impetiginised atopic eczema • superinfected or impe... | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Trial protocol: DE (Completed) | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2020-003406-31 | Sponsor Protocol Number: CCMK389B12201 | Start Date*: 2021-01-10 | |||||||||||
Sponsor Name:Novartis Pharma AG | |||||||||||||
Full Title: A randomized, subject and investigator blinded, placebo-controlled multicenter study to assess the efficacy and safety of CMK389 in patients with moderate to severe atopic dermatitis | |||||||||||||
Medical condition: Moderate to Severe Atopic Dermatitis | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: HU (Completed) DE (Completed) FR (Completed) CZ (Completed) ES (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2014-003725-17 | Sponsor Protocol Number: D2213C00001 | Start Date*: 2015-04-15 | |||||||||||
Sponsor Name:MedImmune | |||||||||||||
Full Title: A Phase 2b, Randomized, Double-blinded, Placebo-controlled, Dose-ranging Study to Evaluate the Efficacy and Safety of Tralokinumab in Adult Subjects with Moderate-to-Severe Atopic Dermatitis | |||||||||||||
Medical condition: Atopic Dermatitis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) PL (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2006-001472-20 | Sponsor Protocol Number: LEO19123-C21 | Start Date*: 2006-08-15 | |||||||||||
Sponsor Name:LEO Pharma A/S | |||||||||||||
Full Title: LEO19123 Cream in the Treatment of Atopic Dermatitis A Phase II, proof of concept study, testing once daily use of two dose-combinations of LEO19123 cream (calcipotriol and LEO80122) in the treatm... | |||||||||||||
Medical condition: Atopic dermatitis | |||||||||||||
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Population Age: Adults | Gender: Male | ||||||||||||
Trial protocol: DK (Completed) FI (Completed) GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2006-003667-31 | Sponsor Protocol Number: TUD_PROVE_001 | Start Date*: 2007-03-30 | |||||||||||
Sponsor Name:Medical Faculty, TU Dresden | |||||||||||||
Full Title: Prednisolone vs. Ciclosporine in Severe Atopic Eczema. PROVE - Study | |||||||||||||
Medical condition: atopic eczema | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Prematurely Ended) AT (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2012-000946-37 | Sponsor Protocol Number: R668-AD-1121 | Start Date*: 2012-06-13 | |||||||||||
Sponsor Name:Regeneron Pharmaceuticals, Inc. | |||||||||||||
Full Title: A randomized, double-blind, parallel-group, placebo-controlled study to assess the safety of REGN668 administered concomitantly with topical corticosteroids to patients with moderate-to-severe Atop... | |||||||||||||
Medical condition: Atopic dermatitis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: HU (Completed) DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2019-001227-12 | Sponsor Protocol Number: M19-850 | Start Date*: 2020-03-13 | |||||||||||
Sponsor Name:AbbVie Deutschland GmbH & Co. KG | |||||||||||||
Full Title: A Phase 3b, open label treatment extension study of upadacitinib for the treatment of adult subjects with moderate to severe atopic dermatitis who successfully completed treatment in the M16-046 study | |||||||||||||
Medical condition: Moderate to severe Atopic Dermatitis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IE (Completed) FI (Completed) HU (Completed) CZ (Completed) ES (Ongoing) NL (Completed) FR (Completed) GB (GB - no longer in EU/EEA) HR (Completed) IT (Completed) NO (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2004-002099-40 | Sponsor Protocol Number: 308962 | Start Date*: 2005-01-20 | |||||||||||
Sponsor Name:Schering AG | |||||||||||||
Full Title: Double-blind, randomized, reference-controlled, multicenter, parallel-group study to compare the efficacy and safety of Advantan ointment once daily with Protopic 0.03% ointment twice daily over ma... | |||||||||||||
Medical condition: Atopic dermatitis | |||||||||||||
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Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) IT (Completed) ES (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: 2004-002477-23 | Sponsor Protocol Number: FG-506-06-FR-04 | Start Date*: 2005-04-01 | |||||||||||
Sponsor Name:Fujisawa GmbH | |||||||||||||
Full Title: Comparative, multicentre, randomised, double-blind study to assess the efficacy of tacrolimus 0.1% ointment versus fluticasone 0.005% ointment in adult patients suffering from moderate to severe at... | |||||||||||||
Medical condition: Moderate to severe atopic dermatitis and presenting with so-called "red face" lesions of the head and neck. | |||||||||||||
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Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FI (Completed) BE (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2004-002673-22 | Sponsor Protocol Number: 309189 | Start Date*: 2005-03-11 | |||||||||||
Sponsor Name:Schering AG | |||||||||||||
Full Title: Double-blind, placebo controlled, randomized, multicenter, parallel-group study to compare the efficacy and safety of Advantan cream twice weekly with Advabas cream during a maintenance phase of 16... | |||||||||||||
Medical condition: Atopic Dermatitis | |||||||||||||
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Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) IT (Completed) ES (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2007-002133-36 | Sponsor Protocol Number: 1401920 | Start Date*: Information not available in EudraCT | |||||||||||
Sponsor Name:INTENDIS GmbH | |||||||||||||
Full Title: A multicenter, randomized, double-blind clinical study to examine the efficacy and safety of Zarzenda® in comparison to Elidel® in the management of mild to moderate atopic dermatitis in children a... | |||||||||||||
Medical condition: Mild to moderate atopic dermatitis. | |||||||||||||
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Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) ES (Completed) IT (Completed) | |||||||||||||
Trial results: (No results available) |
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: 2022-001528-14 | Sponsor Protocol Number: 67484703ADM2001 | Start Date*: 2023-04-03 | |||||||||||
Sponsor Name:Janssen-Cilag International NV | |||||||||||||
Full Title: A Phase 2a, Multi-Center, Randomized, Double-Blind, Placebo-Controlled, Proof of Concept Study to Evaluate the Efficacy, Safety and Tolerability of JNJ-67484703 in Participants with Atopic Dermatitis | |||||||||||||
Medical condition: Atopic Dermatitis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: PL (Completed) DE (Completed) | |||||||||||||
Trial results: (No results available) |
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