- Trials with a EudraCT protocol (6)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
6 result(s) found for: Nummular dermatitis.
Displaying page 1 of 1.
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: 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: 2019-003162-41 | Sponsor Protocol Number: SGZ-2018-12012 | Start Date*: 2021-02-10 | |||||||||||
Sponsor Name:Klinikum rechts der Isar, Technische Universität München | |||||||||||||
Full Title: An investigator-initiated, multi-center, randomized, double-blind, placebo controlled study of Dupilumab to demonstrate efficacy in subjects with nummular eczema | |||||||||||||
Medical condition: Subjects with nummular eczema | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2020-003977-23 | Sponsor Protocol Number: C3941002 | Start Date*: 2021-03-19 | ||||||||||||||||
Sponsor Name:Pfizer Inc. | ||||||||||||||||||
Full Title: A PHASE 2A, RANDOMIZED, DOUBLE BLIND, VEHICLE CONTROLLED, PARALLEL GROUP STUDY TO ASSESS THE EFFICACY, SAFETY, TOLERABILITY AND PHARMACOKINETICS OF PF-07038124 OINTMENT FOR 6 WEEKS IN PARTICIPANTS ... | ||||||||||||||||||
Medical condition: Mild to moderate atopic dermatitis or mild to moderate plaque psoriasis | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: PL (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2017-000610-26 | Sponsor Protocol Number: MK-4117-202 | Start Date*: 2017-02-09 | |||||||||||||||||||||
Sponsor Name:Merck Sharp & Dohme Corp., a subsidiary of Merck & Co., Inc. | |||||||||||||||||||||||
Full Title: A Phase III, Multicenter, Open-Label Long-Term Trial to Study the Efficacy and Safety of MK-4117 in Japanese Subjects With Eczema/Dermatitis and Dermal Pruritus. | |||||||||||||||||||||||
Medical condition: Eczema/dermatitis and the dermal pruritus (itchy skin disease) | |||||||||||||||||||||||
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Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: Outside EU/EEA | |||||||||||||||||||||||
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 |
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