- Trials with a EudraCT protocol (42)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
42 result(s) found for: Dermatitis AND Healthy.
Displaying page 1 of 3.
| 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: View results | |||||||||||||
| EudraCT Number: 2020-000252-35 | Sponsor Protocol Number: DA-TCS-AD | Start Date*: 2020-07-09 | ||||||||||||||||
| Sponsor Name:Lone Skov | ||||||||||||||||||
| Full Title: The risk of an elevated intraocular pressure after treatment with topical corticosteroids in the periocular region | ||||||||||||||||||
| Medical condition: Intraocular pressure in healthy individuals and in patients with atopic dermatitis | ||||||||||||||||||
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| Population Age: Adults | Gender: Male, Female | |||||||||||||||||
| Trial protocol: DK (Completed) | ||||||||||||||||||
| Trial results: View results | ||||||||||||||||||
| EudraCT Number: 2017-002223-25 | Sponsor Protocol Number: NL60891.091.17 | Start Date*: 2018-05-25 | ||||||||||||||||
| Sponsor Name:Radboud University Medical Center | ||||||||||||||||||
| Full Title: Pilot study on the effect of prophylactic versus therapeutic treatment with coal tar and vaseline lanette ointment on the skin barrier repair mechanisms in absence of a chronic inflammatory compone... | ||||||||||||||||||
| Medical condition: Atopic dermatits | ||||||||||||||||||
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| Population Age: Adults | Gender: Male, Female | |||||||||||||||||
| Trial protocol: NL (Ongoing) | ||||||||||||||||||
| Trial results: (No results available) | ||||||||||||||||||
| EudraCT Number: 2024-000164-37 | Sponsor Protocol Number: LPS17250 | Start Date*: 2024-04-09 | |||||||||||
| Sponsor Name:Sanofi (China) Investment Co., Ltd, Shanhai Branch | |||||||||||||
| Full Title: Open-label exploratory study to evaluate the effect of dupilumab on skin barrier function in Chinese patients with moderate to severe atopic dermatitis | |||||||||||||
| Medical condition: Atopic Dermatitis | |||||||||||||
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| Population Age: Adolescents, Under 18, Adults | Gender: Male, Female | ||||||||||||
| Trial protocol: Outside EU/EEA | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2024-000402-15 | Sponsor Protocol Number: LPS17244 | Start Date*: 2024-09-05 | |||||||||||
| Sponsor Name:Sanofi (China) Investment Co., Ltd, Shanhai Branch | |||||||||||||
| Full Title: Open-label exploratory study to evaluate the effect of dupilumab on skin barrier function in Chinese pediatric patients with moderate-to-severe atopic dermatitis | |||||||||||||
| Medical condition: Atopic Dermatitis | |||||||||||||
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| Population Age: Children, Under 18 | Gender: Male, Female | ||||||||||||
| Trial protocol: Outside EU/EEA | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2020-005900-21 | Sponsor Protocol Number: 77474462ADM2003 | Start Date*: 2021-12-08 | |||||||||||
| Sponsor Name:Janssen-Cilag International NV | |||||||||||||
| Full Title: A Phase 2a, Multicenter, Randomized, Placebo-Controlled, Double-Blind, Interventional Study to Assess the Efficacy, Safety, Pharmacokinetics, and Immunogenicity of Multiple IV doses of Bermekimab f... | |||||||||||||
| Medical condition: Moderate to Severe Atopic Dermatitis | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DE (Prematurely Ended) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2020-003542-36 | Sponsor Protocol Number: LPS16763 | Start Date*: 2021-01-19 | |||||||||||
| Sponsor Name:Sanofi-aventis Recherche & Développement | |||||||||||||
| Full Title: A multi-center, exploratory study to assess dupilumab effect on pruritus neuro-mechanisms in patients with atopic dermatitis | |||||||||||||
| Medical condition: Atopic Dermatitis | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DE (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2010-022280-35 | Sponsor Protocol Number: SSD113434 | Start Date*: 2010-11-22 | |||||||||||
| Sponsor Name:GlaxoSmithKline | |||||||||||||
| Full Title: A randomised, double-blind, placebo-controlled study of topical GW870086X formulation in subjects with moderate or severe atopic dermatitis. | |||||||||||||
| Medical condition: subjects with moderate or severe atopic dermatitis. | |||||||||||||
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| Population Age: Adults | Gender: Male, Female | ||||||||||||
| Trial protocol: DE (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2010-022864-12 | Sponsor Protocol Number: AA-10-1.01 | Start Date*: 2011-04-20 | ||||||||||||||||||||||||||
| Sponsor Name:Medical Faculty, Otto-von-Guericke-University Magdeburg | ||||||||||||||||||||||||||||
| Full Title: Effect of Omalizumab (Xolair) on the threshold of degranulation and the composition of intracellular granules in skin mast cells and peripheral basophilic granulocytes before and during omalizumab ... | ||||||||||||||||||||||||||||
| Medical condition: Disease to be investigated: 12 patients with severe chronic urticaria (CU) with or without angioedema which continously need medical treatment As a control: 6 patients with atopy syndrome consisti... | ||||||||||||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||
| Trial protocol: DE (Completed) | ||||||||||||||||||||||||||||
| Trial results: View results | ||||||||||||||||||||||||||||
| EudraCT Number: 2014-003689-26 | Sponsor Protocol Number: CLS001-CO-PR-00;CHDR1428 | Start Date*: 2015-04-16 | ||||||||||||||||
| Sponsor Name:Cutanea Life Sciences | ||||||||||||||||||
| Full Title: A randomized, double-blind, placebo controlled study to assess the pharmacodynamics, safety/tolerability and efficacy of omiganan in patients with mild to moderate atopic dermatitis | ||||||||||||||||||
| Medical condition: Patients with mild to moderate atopic dermatitis. | ||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
| Trial protocol: NL (Completed) | ||||||||||||||||||
| Trial results: (No results available) | ||||||||||||||||||
| EudraCT Number: 2016-000331-41 | Sponsor Protocol Number: CHDR1430 | Start Date*: 2016-03-22 | |||||||||||
| Sponsor Name:Centre for Human Drug Research | |||||||||||||
| Full Title: A randomized, open-label, vehicle-controlled, parallel, dose-ranging study to assess the pharmacodynamics of topically applied Imiquimod in healthy volunteers | |||||||||||||
| Medical condition: none, this is a study on healthy volunteers | |||||||||||||
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| Population Age: Adults | Gender: Male | ||||||||||||
| Trial protocol: NL (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2020-001518-40 | Sponsor Protocol Number: LPS16764 | Start Date*: 2020-12-15 | |||||||||||
| Sponsor Name:Sanofi Aventis Recherche & Developpement | |||||||||||||
| Full Title: Open-label exploratory study to evaluate the effect of dupilumab on skin barrier function in pediatric patients with moderate to severe atopic dermatitis | |||||||||||||
| Medical condition: Atopic dermatitis | |||||||||||||
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| Population Age: Children, Under 18 | Gender: Male, Female | ||||||||||||
| Trial protocol: GB (GB - no longer in EU/EEA) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2020-000314-15 | Sponsor Protocol Number: LPS15991 | Start Date*: 2021-08-17 | |||||||||||
| Sponsor Name:Sanofi-Aventis Recherche & Développement | |||||||||||||
| Full Title: Open label exploratory study to evaluate the effect of dupilumab on skin barrier function in patients with moderate to severe atopic dermatitis | |||||||||||||
| Medical condition: Atopic dermatitis | |||||||||||||
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| Population Age: Adolescents, Under 18, Adults | Gender: Male, Female | ||||||||||||
| Trial protocol: Outside EU/EEA | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2020-000229-24 | Sponsor Protocol Number: RD.06.SPR.201593 | Start Date*: 2021-02-23 | |||||||||||
| Sponsor Name:Galderma S.A. | |||||||||||||
| Full Title: An Open-label Drug-Drug Interaction Study to Assess the Effects of Nemolizumab on Cytochrome P450 Substrates in Subjects 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: BG (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2020-002587-31 | Sponsor Protocol Number: 77474462ADM2001 | Start Date*: 2021-05-06 | |||||||||||
| Sponsor Name:Janssen-Cilag International NV | |||||||||||||
| Full Title: A Phase 2b, Multicenter, Randomized, Placebo- and Active-comparator-controlled, Double-blind Study to Evaluate the Safety and Efficacy of Bermekimab (JNJ-77474462) for the Treatment of Participants... | |||||||||||||
| Medical condition: Moderate to Severe Atopic Dermatitis | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DE (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2013-000629-30 | Sponsor Protocol Number: 06022013 | Start Date*: 2013-04-09 | |||||||||||
| Sponsor Name:Department of surgery, Herlev Hospital | |||||||||||||
| Full Title: The sun protective effect of melatonin: a randomized, placebo-controlled, double-blinded study on healthy volunteers. | |||||||||||||
| Medical condition: Erythema after sun exposure in healthy volunteers | |||||||||||||
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| Population Age: Adults | Gender: Male, Female | ||||||||||||
| Trial protocol: DK (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2016-000376-26 | Sponsor Protocol Number: ZPL521/101 | Start Date*: 2016-05-09 | |||||||||||
| Sponsor Name:Ziarco Pharma Ltd | |||||||||||||
| Full Title: A Randomised, Adaptive Design, Double-Blind (3rd Party Open), Placebo Controlled, Sequential Group Study to Determine the Safety, Tolerability, Pharmacokinetics and Efficacy of Twice Daily Applica... | |||||||||||||
| Medical condition: Atopic Dermatitis | |||||||||||||
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| Population Age: Adults | Gender: Male, Female | ||||||||||||
| Trial protocol: GB (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2020-003639-41 | Sponsor Protocol Number: UP0089 | Start Date*: 2020-11-06 | |||||||||||
| Sponsor Name:UCB Biopharma SRL | |||||||||||||
| Full Title: Phase 1/2A, randomized, placebo-controlled, single-ascending dose (Part A, participant- and investigator-blind) and repeated-dose (Part B, participant-, investigator-, and sponsor-blind) study to i... | |||||||||||||
| Medical condition: Atopic Dermatitis | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: GB (GB - no longer in EU/EEA) NL (Completed) BG (Completed) DE (Completed) ES (Ongoing) BE (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2016-004702-34 | Sponsor Protocol Number: CLS001-CO-PR-015 | Start Date*: 2017-01-09 | |||||||||||
| Sponsor Name:Cutanea Life Sciences | |||||||||||||
| Full Title: A randomized, evaluator-blinded, vehicle-controlled study to explore the pharmacodynamic effects of omiganan and omiganan in combination with imiquimod in healthy volunteers. | |||||||||||||
| Medical condition: None | |||||||||||||
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| Population Age: Adults | Gender: Male, Female | ||||||||||||
| Trial protocol: NL (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2011-000917-38 | Sponsor Protocol Number: CBPR277X2101 | Start Date*: 2011-09-14 | ||||||||||||||||
| Sponsor Name:Novartis Pharma Services AG | ||||||||||||||||||
| Full Title: A first–in-human study to evaluate safety and tolerability of repeated topical administrations of BPR277 ointment in healthy volunteers, and safety, tolerability, and preliminary efficacy of multip... | ||||||||||||||||||
| Medical condition: Part 2: Atopic Dermatitis (AD) Part 3: Netherton Syndrome (NS) | ||||||||||||||||||
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| Population Age: Adults | Gender: Male, Female | |||||||||||||||||
| Trial protocol: DE (Completed) NL (Prematurely Ended) | ||||||||||||||||||
| Trial results: View results | ||||||||||||||||||
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