- Trials with a EudraCT protocol (307)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
307 result(s) found for: Atopic dermatitis.
Displaying page 5 of 16.
| EudraCT Number: 2022-000434-42 | Sponsor Protocol Number: M22-000 | Start Date*: 2022-08-09 | |||||||||||
| Sponsor Name:AbbVie Deutschland GmbH & Co. KG | |||||||||||||
| Full Title: A Phase 3b/4 Randomized, Double-blind, Dose-Flexibility Study of Upadacitinib in Adult Subjects with Moderate to Severe Atopic Dermatitis (Flex-Up) | |||||||||||||
| Medical condition: Moderate to Severe Atopic Dermatitis | |||||||||||||
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| Population Age: Adults | Gender: Male, Female | ||||||||||||
| Trial protocol: HU (Trial now transitioned) IT (Trial now transitioned) ES (Ongoing) PT (Trial now transitioned) BE (Trial now transitioned) DE (Trial now transitioned) SK (Trial now transitioned) FR (Completed) NL (Trial now transitioned) BG (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2018-000747-76 | Sponsor Protocol Number: LP0162-1346 | Start Date*: 2018-11-20 | |||||||||||
| Sponsor Name:LEO Pharma A/S | |||||||||||||
| Full Title: A randomised, double-blind, placebo-controlled, parallel-group, multi-centre, phase 3 trial investigating the efficacy, safety, and tolerability of tralokinumab administered in combination with top... | |||||||||||||
| Medical condition: Atopic Dermatitis | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: FR (Completed) DE (Completed) BE (Completed) GB (Completed) ES (Completed) CZ (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2005-003644-59 | Sponsor Protocol Number: CASM981CDE17 | Start Date*: 2006-11-21 | |||||||||||
| Sponsor Name:University of Heidelberg | |||||||||||||
| Full Title: A two months study of the utility of Elidel cream 1% (pimecrolimus) in the long term management of atopic hand eczema. | |||||||||||||
| Medical condition: chronically relapsing atopic hand eczema | |||||||||||||
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| Population Age: Adults | Gender: Male, Female | ||||||||||||
| Trial protocol: DE (Ongoing) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2008-005890-37 | Sponsor Protocol Number: K201-I/280301BS | Start Date*: 2008-12-30 | |||||||||||
| Sponsor Name:Moberg Derma AB | |||||||||||||
| Full Title: Assessment of the effects on barrier impairment, clinical features and bacterial colonization of topical formulations in patients with atopic eczema; a phase IIa, single-center, randomized, observe... | |||||||||||||
| Medical condition: To assess the barrier impairment, clinical skin condition and bacterial colonization in patients with atopic eczema | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DE (Completed) | |||||||||||||
| 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: 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: 2009-011132-34 | Sponsor Protocol Number: AMC-MS-MTX-001 | Start Date*: 2009-07-06 | |||||||||||
| Sponsor Name:Academic Medical Center, Department of dermatology | |||||||||||||
| Full Title: A 24 week multinational multi-center study consisting of a 12-week single blind study to evaluate the efficacy and safety of methotrexate versus Azathioprin treatment in adult patients with chronic... | |||||||||||||
| Medical condition: Patients with severe atopic dermatitis, defined as a score of 8-9 on the Rajka and Langeland criteria who are unresponsive, intolerant or contra-indicated to cyclisporin treatment. | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: NL (Ongoing) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2006-006462-42 | Sponsor Protocol Number: REP-EC-001 | Start Date*: 2008-01-15 | |||||||||||
| Sponsor Name:Astellas Pharma Europe B.V | |||||||||||||
| Full Title: A PHASE IV, OPEN LABEL, PILOT STUDY OF THE TREATMENT OF CHILDREN WITH MODERATE TO SEVERE ATOPIC DERMATITIS (AD) USING LOCOBASE REPAIR® AS AN ADJUNCTIVE TO STANDARD TREATMENT | |||||||||||||
| Medical condition: Atopic dermatitis | |||||||||||||
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| Population Age: Infants and toddlers, Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
| Trial protocol: GB (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2004-001644-80 | Sponsor Protocol Number: FG-506-06-41 | Start Date*: 2004-12-15 | |||||||||||
| Sponsor Name:Fujisawa GmbH | |||||||||||||
| Full Title: Clinical study on tacrolimus ointment over the long-term “Control Study - Children” Revised version of FG-506-06-39 | |||||||||||||
| Medical condition: Atopic Dermatitis | |||||||||||||
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| Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
| Trial protocol: HU (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2008-005360-14 | Sponsor Protocol Number: FLUTIDANENES08 | Start Date*: 2009-06-23 | |||||||||||
| Sponsor Name:Elena Rubio. Consorcio Hospital General Universitario de Valencia | |||||||||||||
| Full Title: Ensayo clínico aleatorizado, doble ciego con propionato de fluticasona tópico 2 veces por semana, como tratamiento de mantenimiento, para reducir el riesgo de recidivas de dermatitis atópica leve o... | |||||||||||||
| Medical condition: Dermatitis Atópica | |||||||||||||
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| Population Age: Children, Under 18 | Gender: Male, Female | ||||||||||||
| Trial protocol: ES (Prematurely Ended) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2005-002471-32 | Sponsor Protocol Number: S173-GB-01 | Start Date*: Information not available in EudraCT | |||||||||||
| Sponsor Name:Stiefel Laboratories Maidenhead Ltd (commonly known as Stiefel International R&D) | |||||||||||||
| Full Title: A PHASE II, SINGLE-CENTRE, INVESTIGATOR-BLIND, PARALLEL GROUP CLINICAL TRIAL TO INVESTIGATE THE EFFICACY AND SAFETY OF 1% CICLOPIROX OLAMINE (BATRAFEN® CREAM), COMPARED TO 1% HYDROCORTISONE ACETATE... | |||||||||||||
| Medical condition: Mild to moderate atopic eczema | |||||||||||||
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| Population Age: Children, Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: GB (GB - no longer in EU/EEA) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2005-004259-37 | Sponsor Protocol Number: CASM981CDE20 | Start Date*: 2005-12-16 | |||||||||||
| Sponsor Name:Novartis Pharma GmbH | |||||||||||||
| Full Title: An uncontrolled, multicenter 12 month long term study on skin reconstitution with Elidel® (pimecrolimus) 1% cream in adult patients with atopic eczema and corticosteroid induced skin damage | |||||||||||||
| Medical condition: atopic eczema | |||||||||||||
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| Population Age: Adults | Gender: Male, Female | ||||||||||||
| Trial protocol: DE (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2017-000984-34 | Sponsor Protocol Number: 6630-9170-917016 | Start Date*: 2018-05-24 | |||||||||||||||||||||
| Sponsor Name:Medice Arzneimittel Pütter GmbH & Co KG | |||||||||||||||||||||||
| Full Title: A multi-center, randomized, double-blind, phase II trial with intraindividual comparison to assess superiority of Soventol HydroCortisonACETAT 1 % Cremogel versus vehicle on lesional skin in patien... | |||||||||||||||||||||||
| Medical condition: atopic dermatitis, seborrheic eczema or stasis dermatitis | |||||||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
| Trial protocol: DE (Completed) | |||||||||||||||||||||||
| Trial results: View results | |||||||||||||||||||||||
| EudraCT Number: 2017-005143-33 | Sponsor Protocol Number: LP0162-1334 | Start Date*: 2018-11-23 | |||||||||||
| Sponsor Name:LEO Pharma A/S | |||||||||||||
| Full Title: A randomised, double-blind, placebo-controlled, parallel-group, multi-centre trial to evaluate the efficacy, safety, and tolerability of tralokinumab monotherapy in adolescent subjects with moderat... | |||||||||||||
| Medical condition: Atopic Dermatitis | |||||||||||||
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| Population Age: Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
| Trial protocol: FR (Completed) PL (Completed) DE (Completed) NL (Completed) BE (Completed) GB (GB - no longer in EU/EEA) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2014-002194-10 | Sponsor Protocol Number: RV4421A2013147 | Start Date*: 2014-11-10 | |||||||||||
| Sponsor Name:Pierre Fabre Dermo-Cosmétique | |||||||||||||
| Full Title: An intra-individual randomized controlled study to evaluate the efficacy and tolerance of the product RV4421A BS0042 in association with a moderately potent topical corticosteroid in adults with At... | |||||||||||||
| Medical condition: Atopic Dermatitis (arms, popliteal fossa) | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DE (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2013-003001-26 | Sponsor Protocol Number: 2009 | Start Date*: 2013-12-23 | |||||||||||
| Sponsor Name:University of Bristol | |||||||||||||
| Full Title: Choice Of Moisturiser in Eczema Treatment (COMET): A feasibility study of pragmatic, single blind, randomised clinical trial to compare the clinical and cost effectiveness of leave-on emollients in... | |||||||||||||
| Medical condition: Eczema | |||||||||||||
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| Population Age: Infants and toddlers, Children, Under 18 | Gender: Male, Female | ||||||||||||
| Trial protocol: GB (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2013-000715-25 | Sponsor Protocol Number: 6520-9170-07 | Start Date*: 2013-07-23 | |||||||||||||||||||||
| Sponsor Name:MEDICE Arzneimittel Pütter GmbH & Co.KG | |||||||||||||||||||||||
| Full Title: A multi-center, randomized, double-blind, phase II trial with intraindividual comparison to assess superiority of Soventol HydroCort 1% cream versus vehicle on lesional skin in patients with mild a... | |||||||||||||||||||||||
| Medical condition: manifest atopic dermatitis diagnosed according to Hanifin and Rajka, or seborrheic eczema or stasis dermatitis | |||||||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
| Trial protocol: DE (Completed) | |||||||||||||||||||||||
| Trial results: View results | |||||||||||||||||||||||
| EudraCT Number: 2007-004652-36 | Sponsor Protocol Number: 2007-476 | Start Date*: 2008-08-04 | |||||||||||
| Sponsor Name:HOSPICES CIVILS DE LYON | |||||||||||||
| Full Title: Étude randomisée multicentrique de l’efficacité du méthotrexate (MTX) comprimés versus ciclosporine (Cy) capsules dans la dermatite atopique (DA) de forme modérée à sévère de l’adulte | |||||||||||||
| Medical condition: Dermatite atopique | |||||||||||||
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| Population Age: | Gender: Male, Female | ||||||||||||
| Trial protocol: FR (Ongoing) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2007-007267-25 | Sponsor Protocol Number: C07-38 | Start Date*: 2008-06-02 | |||||||||||
| Sponsor Name:INSERM | |||||||||||||
| Full Title: Immunothérapie par vaccination anti-rougeoleuse chez l'adulte atteint de dermatite atopique | |||||||||||||
| Medical condition: Adultes (hommes, femmes) porteurs de Dermatite Atopique (DA) modérée à sévère (SCORAD supérieur ou égal à 15). | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: FR (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2013-003254-24 | Sponsor Protocol Number: R668-AD-1224 | Start Date*: 2015-03-12 | |||||||||||
| Sponsor Name:Regeneron Pharmaceuticals, Inc. | |||||||||||||
| Full Title: A RANDOMIZED, DOUBLE-BLIND, PLACEBO-CONTROLLED STUDY TO DEMONSTRATE THE EFFICACY AND LONG-TERM SAFETY OF DUPILUMAB IN ADULT PATIENTS WITH MODERATE-TO-SEVERE ATOPIC DERMATITIS | |||||||||||||
| Medical condition: Moderate to severe atopic dermatitis (AD). | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DE (Completed) CZ (Completed) IT (Completed) HU (Completed) NL (Completed) LV (Prematurely Ended) BE (Completed) PL (Completed) ES (Completed) RO (Completed) FR (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
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