- Trials with a EudraCT protocol (341)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
341 result(s) found for: eczema.
Displaying page 2 of 18.
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: 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: 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) |
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: 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: 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: 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: 2018-000746-19 | Sponsor Protocol Number: LP0162-1337 | Start Date*: 2018-11-06 | |||||||||||
Sponsor Name:LEO Pharma A/S | |||||||||||||
Full Title: An open-label, single-arm, multi-centre, long-term extension trial to evaluate the safety and efficacy of tralokinumab in subjects with atopic dermatitis who participated in previous tralokinumab c... | |||||||||||||
Medical condition: Atopic Dermatitis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Ongoing) GB (GB - no longer in EU/EEA) DE (Completed) PL (Completed) BE (Completed) CZ (Completed) IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2013-004589-32 | Sponsor Protocol Number: 7724 | Start Date*: 2014-05-07 | |||||||||||
Sponsor Name:University of Southampton | |||||||||||||
Full Title: Bath Additives for the Treatment of cHildhood Eczema (BATHE) | |||||||||||||
Medical condition: Childhood Eczema | |||||||||||||
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Population Age: Children, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2004-002478-47 | Sponsor Protocol Number: FG-506-06-FR-05 | Start Date*: 2005-04-06 | |||||||||||
Sponsor Name:Fujisawa GmbH | |||||||||||||
Full Title: Comparative, multicentre, randomised, double-blind study to assess the efficacy of tacrolimus 0.03% ointment versus fluticasone 0.005% ointment in children aged 2 years or over suffering from moder... | |||||||||||||
Medical condition: Moderate to severe atopic dermatitis | |||||||||||||
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Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: FI (Completed) BE (Completed) | |||||||||||||
Trial results: (No results available) |
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: 2016-004200-65 | Sponsor Protocol Number: LP0162-1325 | Start Date*: 2017-06-28 | |||||||||||
Sponsor Name:LEO Pharma A/S | |||||||||||||
Full Title: A randomised, double-blind, placebo-controlled, phase 3 trial to evaluate the efficacy and safety of tralokinumab monotherapy in subjects with moderate to severe atopic dermatitis who are candidate... | |||||||||||||
Medical condition: Atopic Dermatitis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Completed) FR (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2021-006707-15 | Sponsor Protocol Number: UNI50001-202 | Start Date*: 2022-04-21 | |||||||||||
Sponsor Name:UNION therapeutics A/S | |||||||||||||
Full Title: A Randomized, Double-Blind, Placebo-Controlled, Parallel-Group, Phase 2b Dose-Ranging Study to Evaluate the Efficacy and Safety of Orismilast in Adults 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: DE (Completed) HU (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2008-005469-67 | Sponsor Protocol Number: T&R.SKINP.02 | Start Date*: 2009-01-20 | |||||||||||
Sponsor Name:Thornton & Ross Limited | |||||||||||||
Full Title: A multi-centre, double-blind, vehicle-controlled, randomised group-comparative study to evaluate the efficacy and safety of Altoderm, a topically applied sodium cromoglicate lotion, in the treatmen... | |||||||||||||
Medical condition: Paediatric atopic dermatitis | |||||||||||||
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Population Age: Children, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: (No results available) |
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: 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: 2006-006653-27 | Sponsor Protocol Number: BF37-CT-001 | Start Date*: 2007-04-20 | |||||||||||
Sponsor Name:Biofrontera Bioscience GmbH | |||||||||||||
Full Title: Phase IIa, single-center, randomized, double-blind, vehicle-controlled study to determine the efficacy and safety/tolerability of a topical riluzole formulation in patients with atopic eczema | |||||||||||||
Medical condition: Subjects with mild to moderate dermatitis meeting Hanafin and Rajka´s Criteria with at least two comparable lesional areas of 20-50 cm2. | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2009-010498-19 | Sponsor Protocol Number: RD.03.SPR.40088 | Start Date*: 2009-07-06 | |||||||||||
Sponsor Name:Galderma R&D SNC | |||||||||||||
Full Title: A MULTICENTER, RANDOMIZED, INTRA-INDIVIDUAL, DOUBLE BLIND, VEHICLE-CONTROLLED STUDY TO EVALUATE THE EFFICACY AND SAFETY OF CD2027 OINTMENT 9µG/G APPLIED TWICE DAILY OVER 4 WEEKS IN THE TREATMENT OF... | |||||||||||||
Medical condition: Atopic Dermatitis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Completed) HU (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 |
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