- Trials with a EudraCT protocol (341)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (39)
341 result(s) found for: eczema.
Displaying page 11 of 18.
EudraCT Number: 2006-000292-15 | Sponsor Protocol Number: S241-GB-10 | Start Date*: 2006-03-13 | |||||||||||
Sponsor Name:Stiefel Laboratories Maidenhead Ltd. | |||||||||||||
Full Title: A Phase II, Single-Centre, Randomised,Double-Blind, Parallel Group, CPO Solution, Dose Range Finding Study in Subjects with Seborrhoeic Dermatitis of the Scalp | |||||||||||||
Medical condition: Seborrhoeic dermatitis | |||||||||||||
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Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2006-002060-26 | Sponsor Protocol Number: 1401201 | Start Date*: 2006-12-04 | |||||||||||
Sponsor Name:Intendis GmbH | |||||||||||||
Full Title: A double-blind, randomized, vehicle-controlled, 6-week exploratory multicenter pilot study of the efficacy and safety of Azelaic Acid (AzA) 15% gel in the topical treatment of mild to moderate seb... | |||||||||||||
Medical condition: Patients with mild to moderate seborrheic dermatitis of the facial area and meeting the specific eligibility criteria | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2020-000720-19 | Sponsor Protocol Number: IDI01/2020 | Start Date*: 2020-07-22 | |||||||||||
Sponsor Name:IDI FARMACEUTICI SRL | |||||||||||||
Full Title: A prospective, randomized, multicenter, open- label, two-arm and parallel-group Study to evaluate the efficacy and safety of Nicotinamide DS compared to Ciclopirox olamine cream at 1% in patients a... | |||||||||||||
Medical condition: Patients affected by seborrheic dermatitis. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2017-003106-41 | Sponsor Protocol Number: CHDR1733 | Start Date*: 2018-09-05 | |||||||||||
Sponsor Name:Maruho Co., Ltd. | |||||||||||||
Full Title: A phase 2, randomized, vehicle and ketoconazole-controlled, evaluator-blinded, study to explore the efficacy, pharmacodynamics and safety of omiganan 1.75% topical gel BID in patients with mild to ... | |||||||||||||
Medical condition: Mild to moderate facial seborrheic dermatitis. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2019-002771-33 | Sponsor Protocol Number: ATX201-207 | Start Date*: 2019-09-25 | |||||||||||
Sponsor Name:UNION therapeutics A/S | |||||||||||||
Full Title: A Randomized, Double-Blind, Parallel Group, Vehicle-Controlled Phase 2 Study to Evaluate the Safety and Efficacy of Topical ATx201 OINTMENT in Adolescents and Adults with Mild to Moderate Atopic De... | |||||||||||||
Medical condition: Atopic Dermatitis | |||||||||||||
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Population Age: Adolescents, Under 18, Adults | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Prematurely Ended) PL (Completed) BG (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2018-003712-45 | Sponsor Protocol Number: INCB18424-303 | Start Date*: Information not available in EudraCT | |||||||||||
Sponsor Name:Incyte Corporation | |||||||||||||
Full Title: A Phase 3, Double-Blind, Randomized, 8-Week, Vehicle-Controlled Efficacy and Safety Study of Ruxolitinib Cream Followed by a Long Term Safety Extension Period in Adolescents and Adults With Atopic ... | |||||||||||||
Medical condition: Atopic dermatitis | |||||||||||||
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Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) HU (Completed) FR (Completed) PL (Completed) IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2018-003713-18 | Sponsor Protocol Number: INCB18424-304 | Start Date*: Information not available in EudraCT | |||||||||||
Sponsor Name:Incyte Corporation | |||||||||||||
Full Title: A Phase 3, Double-Blind, Randomized, 8-Week, Vehicle-Controlled Efficacy and Safety Study of Ruxolitinib Cream Followed by a Long Term Safety Extension Period in Adolescents and Adults With Atopic ... | |||||||||||||
Medical condition: Atopic dermatitis | |||||||||||||
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Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: CZ (Completed) DE (Completed) BG (Completed) PL (Completed) ES (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2011-004184-79 | Sponsor Protocol Number: NIAD-01 | Start Date*: 2013-05-01 | |||||||||||
Sponsor Name:Dermal Laboratories Limited | |||||||||||||
Full Title: A placebo controlled evaluation of a developmental gel for the treatment of atopic eczema | |||||||||||||
Medical condition: The medical condition to be investigated in this study is atopic eczema, also known as atopic dermatitis. | |||||||||||||
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Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2016-002351-16 | Sponsor Protocol Number: AP-CL-ECZ-PI-006539 | Start Date*: 2017-05-10 | |||||||||||
Sponsor Name:Technische Universität München, Fakultät für Medizin, represented by Dean | |||||||||||||
Full Title: An investigator-initiated, randomized, double-blind, placebo controlled study of Apremilast to demonstrate efficacy in subjects with nummular eczema | |||||||||||||
Medical condition: Nummular Ecema is an idiopathic chronic inflammatory skin disease that occurs throughout all life periods. Diagnose is made primarily clinically in correlation with histological findings. Treatment... | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2021-003543-16 | Sponsor Protocol Number: LP0133-1528 | Start Date*: 2022-07-28 |
Sponsor Name:LEO Pharma A/S | ||
Full Title: A 24 week, randomised, assessor blinded, active-controlled, parallel group, phase 3, 2 arm trial to compare the efficacy and safety of delgocitinib cream 20 mg/g twice-daily with alitretinoin capsu... | ||
Medical condition: Chronic Hand Eczema | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: DE (Completed) IT (Completed) ES (Ongoing) FR (Completed) AT (Completed) PL (Completed) NO (Completed) SK (Completed) | ||
Trial results: View results |
EudraCT Number: 2005-003140-56 | Sponsor Protocol Number: D200 Probørn | Start Date*: 2006-02-10 |
Sponsor Name:Department of Human Nutrition, The Royal Veterinary and Agricultural University | ||
Full Title: Probiotics to infants with atopic dermatitis; an investigation of the effect on eczema, immune system and intestinal microflora, inflammation and permeability. DK-titel Probiotiske bakterier til ... | ||
Medical condition: Infants participating in the clinical trial are suffering from atopic dermatitis | ||
Disease: | ||
Population Age: Infants and toddlers, Under 18 | Gender: Male, Female | |
Trial protocol: DK (Prematurely Ended) | ||
Trial results: (No results available) |
EudraCT Number: 2021-006340-27 | Sponsor Protocol Number: LP0133-1426 | Start Date*: 2022-04-21 | |||||||||||
Sponsor Name:LEO Pharma A/S | |||||||||||||
Full Title: A phase 3 clinical trial to evaluate efficacy and safety of twice daily applications of delgocitinib cream 20 mg/g compared with cream vehicle for a 16-week treatment period in adolescents 12-17 ye... | |||||||||||||
Medical condition: Chronic Hand Eczema | |||||||||||||
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Population Age: Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Completed) ES (Ongoing) BE (Completed) PL (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2017-002176-75 | Sponsor Protocol Number: CZPL389A2203 | Start Date*: 2019-11-05 | |||||||||||
Sponsor Name:Novartis Pharma AG | |||||||||||||
Full Title: A randomized, double blind, placebo controlled multicenter dose ranging study to assess the safety and efficacy of multiple oral ZPL389 doses in patients with moderate to severe Atopic Dermatitis (... | |||||||||||||
Medical condition: Moderate to severe atopic dermatitis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Prematurely Ended) GB (Prematurely Ended) NL (Prematurely Ended) FI (Prematurely Ended) IS (Completed) AT (Prematurely Ended) EE (Prematurely Ended) BE (Prematurely Ended) CZ (Completed) HU (Prematurely Ended) FR (Prematurely Ended) ES (Prematurely Ended) LV (Prematurely Ended) LT (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2018-002401-56 | Sponsor Protocol Number: I9N-MC-FCAB | Start Date*: 2019-04-29 | |||||||||||
Sponsor Name:Eli Lilly & Company | |||||||||||||
Full Title: A Multicenter, Randomized, Double-Blind, Placebo-Controlled, Phase 2 Study to Evaluate the Efficacy and Safety of LY3375880 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: HU (Prematurely Ended) AT (Prematurely Ended) FR (Prematurely Ended) ES (Prematurely Ended) DE (Prematurely Ended) IT (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2008-006844-21 | Sponsor Protocol Number: DELP-01 | Start Date*: 2009-12-01 | |||||||||||
Sponsor Name:Dermal Laboratories Ltd | |||||||||||||
Full Title: Evaluation of a developmental ‘long lasting’ emollient in subjects with dry skin. | |||||||||||||
Medical condition: Eczema sufferers with dry skin. | |||||||||||||
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Population Age: Adults | Gender: Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2018-001136-21 | Sponsor Protocol Number: B7451013 | Start Date*: 2018-10-22 | |||||||||||
Sponsor Name:Pfizer Inc., 235 East 42nd Street, New York, NY 10017 | |||||||||||||
Full Title: A Phase 3 Randomized, Double-Blind, Placebo-Controlled, Parallel Group, Multi-Center Study to Evaluate the Efficacy and Safety of PF-04965842 Monotherapy in Subjects Aged 12 Years and Older, with M... | |||||||||||||
Medical condition: Moderate to severe atopic dermatitis | |||||||||||||
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Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: BG (Completed) HU (Completed) CZ (Completed) GB (Completed) DE (Completed) PL (Completed) LV (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2016-001505-17 | Sponsor Protocol Number: BILA-3716/PRU | Start Date*: 2016-07-29 | |||||||||||||||||||||
Sponsor Name:FAES FARMA, S.A. | |||||||||||||||||||||||
Full Title: An exploratory study to evaluate the efficacy and safety of bilastine in reducing pruritus in patients with chronic spontaneous urticaria and other skin diseases. | |||||||||||||||||||||||
Medical condition: Chronic spontaneous urticaria and the following skin disorders: 1 - Eczema/dermatitis (acute eczema, chronic eczema, contact dermatitis, atopic dermatitis, nummular eczema, autosensitisation dermat... | |||||||||||||||||||||||
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Population Age: Elderly | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: ES (Completed) HU (Completed) | |||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2007-004649-14 | Sponsor Protocol Number: ASF-1057-303 | Start Date*: 2008-02-19 |
Sponsor Name:Astion Pharma A/S | ||
Full Title: Safety of ASF 1057 cream 0.5% under long term use in the treatment of seborrhoeic dermatitis: A 12 month open label extension multi-centre phase III trial | ||
Medical condition: Seborrhoeic dermatitis | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: FR (Ongoing) FI (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2018-004705-26 | Sponsor Protocol Number: LPS15497 | Start Date*: 2020-03-24 | |||||||||||
Sponsor Name:Sanofi Aventis Groupe | |||||||||||||
Full Title: A randomized double blind placebo controlled study evaluating the effect of dupilumab on sleep in adult patients with moderate to severe atopic dermatitis | |||||||||||||
Medical condition: Atopic dermatitis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) DE (Completed) FR (Completed) IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2007-004308-11 | Sponsor Protocol Number: GTG002.07 | Start Date*: 2010-01-11 | |||||||||||
Sponsor Name:Genethon | |||||||||||||
Full Title: PHASE I/II CLINICAL TRIAL OF HAEMATOPOIETIC STEM CELL GENE THERAPY FOR THE WISKOTT-ALDRICH SYNDROME | |||||||||||||
Medical condition: Wiskott-Aldrich syndrome (WAS) is a rare X-linked immunodeficiency caused by mutations in a single gene ,the Wiskott-Aldrich Syndrome Protein (WASP). WAS is characterised by micro-thrombocytopenia,... | |||||||||||||
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Population Age: Infants and toddlers, Children, Adolescents, Under 18 | Gender: Male | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
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