- Trials with a EudraCT protocol (198)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (8)
198 result(s) found for: Topical corticosteroids.
Displaying page 1 of 10.
EudraCT Number: 2018-001726-26 | Sponsor Protocol Number: I4V-MC-JAIY | Start Date*: 2018-11-06 | |||||||||||
Sponsor Name:Eli Lilly and Company | |||||||||||||
Full Title: A Multicenter, Randomized, Double-Blind, Placebo-Controlled, Phase 3 Study to Evaluate the Efficacy and Safety of Baricitinib in Combination with Topical Corticosteroids in Adult Patients with Mode... | |||||||||||||
Medical condition: Atopic Dermatitis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) AT (Completed) ES (Completed) PL (Completed) IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2017-002835-40 | Sponsor Protocol Number: AK701 | Start Date*: 2020-01-28 | ||||||||||||||||||||||||||
Sponsor Name:Akari Therapeutics Plc | ||||||||||||||||||||||||||||
Full Title: Topical rVA576 for treatment of atopic keratoconjunctivitis: a randomised placebo double masked parallel trial (TRACKER) | ||||||||||||||||||||||||||||
Medical condition: Moderate to severe atopic keratoconjunctivitis (AKC), Vernal keratoconjunctivitis (VKC), Severe allergic conjunctivitis (seasonal (SAC) or perennial (PAC)) | ||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||
Trial protocol: ES (Prematurely Ended) | ||||||||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2016-004542-28 | Sponsor Protocol Number: NL59862.091.16 | Start Date*: 2017-09-14 | |||||||||||
Sponsor Name:Radboud University Medical Center | |||||||||||||
Full Title: A randomized controlled pilot study comparing the efficacy of topical coal tar to topical corticosteroids in children aged 1 to < 16 years with moderate-severe atopic dermatitis. | |||||||||||||
Medical condition: Atopic dermatitis | |||||||||||||
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Population Age: Infants and toddlers, Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2016-004687-19 | Sponsor Protocol Number: NL59928.091.16 | Start Date*: 2018-04-23 | |||||||||||
Sponsor Name:Radboud University Medical Center | |||||||||||||
Full Title: A randomized controlled trial evaluating the additional effect of topical coal tar to a topical corticosteroid regimen in patients aged >16 years of age with moderate-severe atopic dermatitis. | |||||||||||||
Medical condition: Atopic Dermatitis (AD) | |||||||||||||
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Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2013-000410-38 | Sponsor Protocol Number: LP0066-1019 | Start Date*: 2013-10-25 | |||||||||||
Sponsor Name:LEO Pharma A/S | |||||||||||||
Full Title: Topical Aprepitant in Prurigo Patients (iTAPP) An exploratory phase IIa trial with topically applied aprepitant in patients with prurigo | |||||||||||||
Medical condition: Prurigo can present either with hyperkeratotic nodules as prurigo nodularis or without nodules as Prurigo simplex. The disease is characterised by intensely pruritic, lichenified, or excoriated pap... | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2004-002688-25 | Sponsor Protocol Number: CASM981CGB02 | Start Date*: 2005-01-07 |
Sponsor Name:Novartis Pharmaceuticals UK Ltd | ||
Full Title: A 4-week, randomized, multicenter, parallel-group, placebo-controlled study to investigate the effect of Elidel (pimecrolimus) cream 1% on the Quality of Life (QoL) of patients with moderate facial... | ||
Medical condition: Atopic Eczema (AE) | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (Completed) | ||
Trial results: View results |
EudraCT Number: 2017-005126-37 | Sponsor Protocol Number: M16-047 | Start Date*: 2018-10-30 | |||||||||||
Sponsor Name:AbbVie Deutschland GmbH & Co. KG | |||||||||||||
Full Title: A Phase 3 Randomized, Placebo-Controlled, Double-Blind Study to Evaluate Upadacitinib in Combination with Topical Corticosteroids in Adolescent and Adult Subjects with Moderate to Severe Atopic De... | |||||||||||||
Medical condition: Moderate and Severe Atopic Dermatitis | |||||||||||||
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Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IE (Trial now transitioned) SE (Trial now transitioned) SK (Trial now transitioned) CZ (Trial now transitioned) HU (Trial now transitioned) DE (Trial now transitioned) FR (Trial now transitioned) BE (Trial now transitioned) NL (Trial now transitioned) GB (GB - no longer in EU/EEA) AT (Trial now transitioned) GR (Trial now transitioned) NO (Trial now transitioned) ES (Ongoing) IT (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2005-002077-76 | Sponsor Protocol Number: QGUY/2005/AER 001/-02 | Start Date*: 2005-06-13 |
Sponsor Name:Aerovance Inc | ||
Full Title: A Phase 2a Study To Investigate The Effects of Repeated Administration of AeroDerm in subjects with Atopic Eczema. | ||
Medical condition: Atopic Eczema: a chronic inflammatory pruritic skin disease that follows a relapsing course and is often associated with elevated serum immunoglobulin E (IgE) levels and a personal or family histor... | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: GB (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2005-005174-68 | Sponsor Protocol Number: UZL OFT-AMO 001 | Start Date*: 2006-04-21 |
Sponsor Name:UZLeuven Afdeling Oogziekten | ||
Full Title: A Double blind Interventional study exploring the efficacy of topical eye treatment in the prevention of Docetaxel induced Dacryostenosis. | ||
Medical condition: The rationale of this randomized double blind study is to investigate the efficacy of topical eye treatment in patients on a weekly Docetaxel regimen in prevention of dacryostenosis. The dacryotoxi... | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: BE (Completed) | ||
Trial results: View results |
EudraCT Number: 2017-004574-34 | Sponsor Protocol Number: I4V-MC-JAIN | Start Date*: 2018-04-05 | |||||||||||
Sponsor Name:Eli Lilly and Company | |||||||||||||
Full Title: A Phase 3, Multicenter, Double-Blind, Randomized, Placebo-Controlled Study Evaluating the Safety and Efficacy of Baricitinib in Combination with Topical Corticosteroids in Adult Patients with Moder... | |||||||||||||
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) FR (Completed) AT (Completed) BE (Completed) PL (Completed) FI (Completed) ES (Ongoing) IT (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: (No results available) |
EudraCT Number: 2015-003804-21 | Sponsor Protocol Number: DFD-07-CD-001 | Start Date*: 2015-11-12 |
Sponsor Name:Promius Pharma LLC | ||
Full Title: Multi-centre, Randomized, Double-blind, Placebo-Controlled Pilot Safety and Efficacy Study of 8 Weeks of Treatment with DFD-07 for Actinic Keratosis of the Face and Scalp | ||
Medical condition: Actinic Keratosis (AK) | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: DE (Completed) | ||
Trial results: View results |
EudraCT Number: 2006-003073-27 | Sponsor Protocol Number: RD.03.SPR29064 | Start Date*: 2007-02-06 | |||||||||||
Sponsor Name:Galderma R&D | |||||||||||||
Full Title: Subject preference comparison between Clobetasol propionate shampoo, 0.05% and three other topical corticosteroids in the treatment of moderate to severe Scalp psoriasis | |||||||||||||
Medical condition: Moderate to Severe Scalp Psoriasis with a Global Severity Score of 3 at least on a scale from 0 to 5. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) IT (Completed) DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2018-002830-19 | Sponsor Protocol Number: RC31-18-0269 | Start Date*: 2018-11-16 |
Sponsor Name: Toulouse University Hospital | ||
Full Title: A randomized, double blind placebo-controlled multicenter study of the efficacy and safety of dupilumab in patients with moderate to severe hand eczema refractory to highly potent topical corticost... | ||
Medical condition: Chronic hand eczema | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: FR (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2016-004997-16 | Sponsor Protocol Number: R668-AD-1652 | Start Date*: 2018-02-09 | |||||||||||
Sponsor Name:Regeneron Pharmaceuticals, Inc. | |||||||||||||
Full Title: A randomized, double-blind, placebo-controlled study to investigate the efficacy and safety of dupilumab administered concomitantly with topical corticosteroids in patients, ≥6 years to <12 years o... | |||||||||||||
Medical condition: Atopic Dermatitis | |||||||||||||
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Population Age: Children, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: CZ (Completed) DE (Completed) GB (Completed) PL (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2004-001036-23 | Sponsor Protocol Number: CASM981C2442 | Start Date*: 2004-11-05 |
Sponsor Name:Novartis Sverige AB | ||
Full Title: A 12-week multicenter study consisting of a 6 week double blind, randomized, vehicle controlled, parallel group phase, followed by a 6 week open label phase, to assess the safety and efficacy of El... | ||
Medical condition: atopic dermatitis (atopic eczema) | ||
Disease: | ||
Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | |
Trial protocol: SE (Completed) IT (Completed) | ||
Trial results: View results |
EudraCT Number: 2006-004876-10 | Sponsor Protocol Number: ASF-EVER.1 | Start Date*: 2007-08-06 | |||||||||||
Sponsor Name:Department of Ophthalmology at St. Franziskus Hospital | |||||||||||||
Full Title: single center study on safety and efficacy of everolimus in patients with endogenous intermediate and posterior uveitis | |||||||||||||
Medical condition: Uveitis, specially endogenous interemdiate and posterior uveitis | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2009-015077-12 | Sponsor Protocol Number: rrk3681 | Start Date*: 2009-11-23 |
Sponsor Name:University Hospital Birmingham NHS Foundation Trust | ||
Full Title: The use of corticosteroids (Budenofalk) as a chemopreventative agent in ulcerative colitis associated neoplasia | ||
Medical condition: chronic ulcerative colitis | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: GB (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2005-001650-25 | Sponsor Protocol Number: CASM981C2440 | Start Date*: 2005-09-26 | |||||||||||
Sponsor Name:Novartis Pharma Services AG | |||||||||||||
Full Title: A 12 week multicenter study consisting of a 6 week double blind, randomized, vehicle controlled, parallel group phase, followed by a 6 week open label phase, to assess the efficacy and safety of El... | |||||||||||||
Medical condition: Mild to moderate facial atopic dermatitis (AD), in children | |||||||||||||
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Population Age: Children, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: SK (Completed) DE (Completed) | |||||||||||||
Trial results: View results |
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 |
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