- Trials with a EudraCT protocol (1,923)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
1,923 result(s) found for: Skin Diseases AND Skin Disease.
Displaying page 15 of 97.
| EudraCT Number: 2021-004315-76 | Sponsor Protocol Number: EFC16973 | Start Date*: 2022-01-13 | |||||||||||
| Sponsor Name:SANOFI-AVENTIS RECHERCHE E DEVELOPPEMENT | |||||||||||||
| Full Title: Master protocol of two randomized, double blind, placebo-controlled, multicenter, parallel group studies to evaluate the efficacy and safety of dupilumab in adult patients with chronic pruritus of ... | |||||||||||||
| Medical condition: Chronic pruritus of unknown origin (CPUO) | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: IT (Trial now transitioned) ES (Ongoing) HU (Trial now transitioned) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2020-001981-13 | Sponsor Protocol Number: INCB54707204 | Start Date*: 2021-03-02 | |||||||||||
| Sponsor Name:Incyte Corporation | |||||||||||||
| Full Title: A Phase 2, Randomized, Double-Blind, Placebo-Controlled, Dose-Ranging Study of the Efficacy and Safety of INCB054707 in Participants With Hidradenitis Suppurativa | |||||||||||||
| Medical condition: Hidradenitis Suppurativa | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: FR (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2021-000003-20 | Sponsor Protocol Number: MEMPSOLAR0001 | Start Date*: 2021-06-08 | |||||||||||
| Sponsor Name:Aarhus University Hospital | |||||||||||||
| Full Title: AN INVESTIGATOR INITIATED, PHASE 4, OPEN-LABEL, SINGLE-ARM, SINGLE-CENTER STUDY INVESTIGATING THE RESIDUAL DISEASE MEMORY IN PSORIASIS SKIN DURING ENSTILAR® AND NARROW-BAND ULTRAVIOLET B THERAPY. ... | |||||||||||||
| Medical condition: Psoriasis vulgaris | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DK (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2020-002912-34 | Sponsor Protocol Number: 20-PP-13 | Start Date*: 2020-08-11 |
| Sponsor Name:CHU NICE | ||
| Full Title: Treatment of bullous pemphigoid with avdoralimab (IPH5401), an anti-C5aR1 monoclonal antibody | ||
| Medical condition: Auto Immune bullous Diseases | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: FR (Completed) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2019-002550-23 | Sponsor Protocol Number: HS0003 | Start Date*: 2020-04-24 | |||||||||||
| Sponsor Name:UCB Biopharma SRL | |||||||||||||
| Full Title: A Phase 3, Randomized, Double-Blind, Placebo-Controlled, Multicenter Study Evaluating the Efficacy and Safety of Bimekizumab in Study Participants With Moderate to Severe Hidradenitis Suppurativa | |||||||||||||
| Medical condition: Hidradenitis Suppurativa | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DE (Completed) GR (Completed) BE (Completed) NL (Completed) DK (Completed) ES (Ongoing) IT (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2012-000253-30 | Sponsor Protocol Number: LP0075-34 | Start Date*: 2012-11-08 | |||||||||||
| Sponsor Name:LEO Pharma A/S | |||||||||||||
| Full Title: An exploratory study evaluating the efficacy of cromoglicate cream compared to cream vehicle in the treatment of itch in psoriasis | |||||||||||||
| Medical condition: itchy psoriasis | |||||||||||||
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| Population Age: Adults | Gender: Male, Female | ||||||||||||
| Trial protocol: DE (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2021-005573-12 | Sponsor Protocol Number: LP0162-1335 | Start Date*: 2022-10-05 | |||||||||||
| Sponsor Name:LEO Pharma A/S | |||||||||||||
| Full Title: A single (assessor) blinded, randomised, parallel-group, monotherapy trial to evaluate the pharmacokinetic and safety of tralokinumab in children (age 2 to <12 years) with moderate-to-severe atopic... | |||||||||||||
| Medical condition: Atopic dermatitis | |||||||||||||
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| Population Age: Children, Under 18 | Gender: Male, Female | ||||||||||||
| Trial protocol: FR (Trial now transitioned) CZ (Trial now transitioned) NL (Trial now transitioned) ES (Ongoing) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2020-005079-12 | Sponsor Protocol Number: CHUBX2019/21 | Start Date*: 2021-03-24 |
| Sponsor Name:Centre Hospitalier Universitaire de Bordeaux | ||
| Full Title: Efficacy and tolerance of the association of baricitinib (4mg) and phototherapy versus phototherapy in adults with progressive vitiligo: a randomized double blind, non comparative phase II study. | ||
| Medical condition: progressive vitiligo | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: FR (Completed) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2006-000363-28 | Sponsor Protocol Number: GBI001 | Start Date*: 2006-10-03 |
| Sponsor Name:Greater Glasgow Health Board [...] | ||
| Full Title: DIFFERENTIATING THE MECHANISM OF ACTION OF ANTI TNF-alpha AGENTS | ||
| Medical condition: Rheumatoid arthritis and Psoriatic arthritis | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: GB (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2014-005594-36 | Sponsor Protocol Number: PHT/2014/107 | Start Date*: 2015-12-15 | |||||||||||
| Sponsor Name:Portsmouth Hospitals NHS Trust | |||||||||||||
| Full Title: A Phase IV, Randomised, Double-Blind, Controlled, Parallel Group Trial to Evaluate the Effectiveness and Safety of Balneum Plus vs Emollient in the Treatment of Uraemic Pruritus in Haemodialysis Pa... | |||||||||||||
| Medical condition: Uraemic Pruritus | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: GB (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2016-001566-28 | Sponsor Protocol Number: UCDCRC/16/002 | Start Date*: 2017-01-11 | |||||||||||
| Sponsor Name:University College Dublin | |||||||||||||
| Full Title: Usage of Omics Technology for Identification of Critical Mediators and Pathways in Patients with Hidradenitis Suppurativa | |||||||||||||
| Medical condition: Hidradenitis Suppurativa | |||||||||||||
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| Population Age: Adults | Gender: Male, Female | ||||||||||||
| Trial protocol: IE (Prematurely Ended) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2010-018640-13 | Sponsor Protocol Number: DERMOPED_001_DA_ISS | Start Date*: 2009-10-28 | |||||||||||
| Sponsor Name:GUNA S.P.A. | |||||||||||||
| Full Title: "Evaluation of Clinical Immunology of a long-term treatment with Physiological Regulating Medicine in a Pediatric Population suffering from chronic atopic dermatitis. Experimental study randomized ... | |||||||||||||
| Medical condition: Atopic dermatitis | |||||||||||||
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| Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
| Trial protocol: IT (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2010-024131-16 | Sponsor Protocol Number: UKM10_0019 | Start Date*: 2011-05-06 | |||||||||||
| Sponsor Name:Universitätsklinikum Münster | |||||||||||||
| Full Title: Efficacy and Safety of oral Alitretinoin (Toctino®) in the Treatment of Patients with Cutaneous Lupus Erythematosus: A Multicentre, Open-Label, Prospective Pilot Study | |||||||||||||
| Medical condition: Αdult subjects of any ethnicity and either gender with Subacute Cutaneous Lupus Erythematosus (SCLE), Discoid Lupus Erythematosus (DLE), Lupus erythematosus tumidus (LET) or Systemic Lupus Erythema... | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DE (Prematurely Ended) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2016-002143-42 | Sponsor Protocol Number: 16013 | Start Date*: 2017-11-08 | |||||||||||
| Sponsor Name:Odense University Hospital | |||||||||||||
| Full Title: A designed Patient-centered Intervention to Improve medical Adherence in Topical Treatment of psoriasis - A Study protocol | |||||||||||||
| Medical condition: Psoriasis | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DK (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2017-003119-21 | Sponsor Protocol Number: 1 | Start Date*: 2017-12-22 |
| Sponsor Name:Medical University of Vienna | ||
| Full Title: Effect of Omalizumab in patients with Aspirin-Exazerbated Respiratory Disease (AERD) | ||
| Medical condition: Aspirin-exacerbated respiratory disease (AERD), also known as Samter's triad or Widal's triad, comprises the triad of Asthma, chronic rhinosinusitis with nasal polyps (CRwNP) and nonsteroidal anti-... | ||
| Disease: | ||
| Population Age: Adults | Gender: Male, Female | |
| Trial protocol: AT (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2018-003051-38 | Sponsor Protocol Number: B7931023 | Start Date*: 2019-08-02 | |||||||||||
| Sponsor Name:Pfizer Inc. | |||||||||||||
| Full Title: A PHASE 2B, RANDOMIZED, DOUBLE BLIND, VEHICLE-CONTROLLED, PARALLEL-GROUP, DOSE RANGING STUDY TO ASSESS EFFICACY, SAFETY, TOLERABILITY AND PHARMACOKINETICS OF PF-06700841 TOPICAL CREAM APPLIED ONCE ... | |||||||||||||
| Medical condition: Plaque psoriasis (PsO) | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: LV (Completed) DE (Completed) HU (Completed) BG (Completed) PL (Completed) DK (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2018-002446-36 | Sponsor Protocol Number: BP40635 | Start Date*: 2018-11-05 | |||||||||||
| Sponsor Name:F. Hoffmann-La Roche Ltd | |||||||||||||
| Full Title: AN OPEN LABEL PHASE 2A TRIAL ASSESSING THE CLINICAL EFFICACY AND SAFETY OF RO5459072 IN MODERATE TO SEVERE PSORIASIS | |||||||||||||
| Medical condition: Psoriasis | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DE (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2014-004467-20 | Sponsor Protocol Number: AVXCLIN002 | Start Date*: 2014-12-10 | |||||||||||
| Sponsor Name:Avexxin AS | |||||||||||||
| Full Title: A Randomized, Double-blind, Placebo-controlled, Sequential Parallel Group, Dose-escalation, Single Centre Study to Assess the Safety and Efficacy of AVX001 when Administered Topically Once Daily in... | |||||||||||||
| Medical condition: Psoriasis vulgaris | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male | ||||||||||||
| Trial protocol: DK (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2014-001581-10 | Sponsor Protocol Number: TCP-101 | Start Date*: 2014-07-22 |
| Sponsor Name:Tigercat Pharma, Inc. | ||
| Full Title: A Phase II, Randomized, Double-Blind, Placebo-Controlled, Dose Finding and Efficacy Study of VPD-737 in the Treatment of Subjects with Chronic Pruritus | ||
| Medical condition: Chronic pruritus | ||
| Disease: | ||
| Population Age: Adults | Gender: Male, Female | |
| Trial protocol: IE (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2017-002332-16 | Sponsor Protocol Number: RC31-16-8917 | Start Date*: 2017-10-03 | |||||||||||
| Sponsor Name:Toulouse Hospital | |||||||||||||
| Full Title: Evaluation of the efficacy of injections of botulinic toxin in plantar lesions of patients suffering from localized epidermolysis bullosa simplex : double blind randomized controlled study. | |||||||||||||
| Medical condition: localized epidermolysis bullosa simplex | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: FR (Prematurely Ended) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
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