- Trials with a EudraCT protocol (44)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
44 result(s) found for: Lupus Erythematosus, Cutaneous.
Displaying page 1 of 3.
EudraCT Number: 2014-005000-19 | Sponsor Protocol Number: CNTO1275SLE2001 | Start Date*: 2015-03-18 | |||||||||||
Sponsor Name:Janssen-Cilag International N.V. | |||||||||||||
Full Title: A Multicenter, Randomized, Double-blind, Placebo-controlled, Proof-of-Concept Study of Ustekinumab in Subjects With Active Systemic Lupus Erythematosus | |||||||||||||
Medical condition: Systemic Lupus Erythematosus | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: HU (Completed) DE (Completed) ES (Completed) PL (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2022-000239-21 | Sponsor Protocol Number: MS200569_0048 | Start Date*: 2022-10-18 | |||||||||||||||||||||
Sponsor Name:Merck Healthcare KGaA | |||||||||||||||||||||||
Full Title: A Phase 2, Double-blind, Dose-Ranging, Parallel, Long-term Extension Study to Evaluate the Safety and Efficacy of Enpatoran in Participants with Subacute Cutaneous Lupus Erythematosus, Discoid Lupu... | |||||||||||||||||||||||
Medical condition: Systemic lupus erythematosus (SLE) and cutaneous lupus erythematosus (CLE) | |||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: BG (Trial now transitioned) ES (Trial now transitioned) RO (Trial now transitioned) | |||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2020-004047-86 | Sponsor Protocol Number: AIS-A03 | Start Date*: Information not available in EudraCT | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Sponsor Name:Alpine Immune Sciences, Inc. | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Full Title: A RANDOMIZED, DOUBLE-BLIND, PLACEBO-CONTROLLED STUDY OF ALPN-101 IN SYSTEMIC LUPUS ERYTHEMATOSUS | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Medical condition: Systemic lupus erythematosus (SLE) | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Trial protocol: FR (Completed) PL (Completed) ES (Prematurely Ended) HU (Completed) | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2020-005776-35 | Sponsor Protocol Number: 230LE304 | Start Date*: 2021-12-24 | ||||||||||||||||
Sponsor Name:Biogen Idec Research Limited | ||||||||||||||||||
Full Title: A Multicenter, Randomized, Double-Blind, Placebo-Controlled, Phase 3 Study to Evaluate the Efficacy and Safety of BIIB059 in Adult Participants With Active Systemic Lupus Erythematosus Receiving Ba... | ||||||||||||||||||
Medical condition: systemic lupus erythematosus | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: NL (Trial now transitioned) DE (Trial now transitioned) HU (Trial now transitioned) CZ (Trial now transitioned) BE (Trial now transitioned) IT (Trial now transitioned) RO (Trial now transitioned) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2020-000071-21 | Sponsor Protocol Number: IM011-132 | Start Date*: 2021-03-18 | |||||||||||||||||||||
Sponsor Name:Bristol-Myers Squibb International Corporation | |||||||||||||||||||||||
Full Title: A Phase 2 Randomized, Double-Blind, Placebo-Controlled Study to Evaluate Efficacy and Safety of BMS-986165 in Participants with Active Discoid and/or Subacute Cutaneous Lupus Erythematosus (DLE/SCLE) | |||||||||||||||||||||||
Medical condition: Active Discoid and/or Subacute Cutaneous Lupus Erythematosus (DLE/SCLE) | |||||||||||||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: FR (Trial now transitioned) | |||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2006-007056-18 | Sponsor Protocol Number: 3403 | Start Date*: 2007-03-16 | |||||||||||
Sponsor Name:The Newcastle upon tyne Hospitals NHS Trust | |||||||||||||
Full Title: The Discoid Lupus Research Project | |||||||||||||
Medical condition: Discoid lupus erythematosus | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2020-005775-12 | Sponsor Protocol Number: 230LE303 | Start Date*: 2021-10-05 | ||||||||||||||||
Sponsor Name:Biogen Idec Research Limited | ||||||||||||||||||
Full Title: A Multicenter, Randomized, Double-Blind, Placebo-Controlled, Phase 3 Study to Evaluate the Efficacy and Safety of BIIB059 in Adult Participants With Active Systemic Lupus Erythematosus Receiving Ba... | ||||||||||||||||||
Medical condition: systemic lupus erythematosus | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: ES (Ongoing) FR (Trial now transitioned) GR (Trial now transitioned) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2021-006378-22 | Sponsor Protocol Number: 230LE306 | Start Date*: 2022-10-04 | ||||||||||||||||
Sponsor Name:Biogen Idec Research Limited | ||||||||||||||||||
Full Title: A Multicenter, Randomized, Dose-Blind, Phase 3 Long-Term Extension Study to Evaluate Continuous Safety and Efficacy of Litifilimab (BIIB059) in Adult Participants with Active Systemic Lupus Erythem... | ||||||||||||||||||
Medical condition: Systemic Lupus Erythematosus | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: BG (Trial now transitioned) PL (Trial now transitioned) NL (Trial now transitioned) HU (Trial now transitioned) CZ (Trial now transitioned) IT (Trial now transitioned) GR (Trial now transitioned) ES (Ongoing) BE (Trial now transitioned) RO (Trial now transitioned) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2008-003833-25 | Sponsor Protocol Number: EFACLE2008 | Start Date*: 2009-02-05 | |||||||||||||||||||||
Sponsor Name:Universitätskrankenhaus Schleswig-Holstein | |||||||||||||||||||||||
Full Title: Efficacy ans safety of subcutaneous Efalizumab in the treatment of patients with cutaneous lupus erythematosus: A mono-centre, open-label, prospective pilot study | |||||||||||||||||||||||
Medical condition: Cutaneous lupus erythematosus (discoid LE or subacute cutaneous LE) or systemic lupus erythematosus with cutaneous DLE or SCLE lesions without major organ involvment. | |||||||||||||||||||||||
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Population Age: | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: DE (Prematurely Ended) | |||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2010-023645-29 | Sponsor Protocol Number: UKM 10_0020 | Start Date*: 2011-03-15 | ||||||||||||||||
Sponsor Name:Universitätsklinikum Münster | ||||||||||||||||||
Full Title: Efficacy and safety of fumaric acid esters in the treatment of patients with cutaneous lupus erythematosus: A monocentre, open-label, prospective pilot study | ||||||||||||||||||
Medical condition: Adult subjects of any ethnicity and either gender with Cutaneous Lupus Erythematosus lesions of Subacute Cutaneous Lupus Erythematosus (SCLE), Discoid Lupus Erythematosus (DLE), Lupus erythematosus... | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: DE (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2021-004648-27 | Sponsor Protocol Number: MS200569_0003 | Start Date*: 2022-03-21 | |||||||||||||||||||||
Sponsor Name:Merck Healthcare KGaA | |||||||||||||||||||||||
Full Title: A Phase II, Randomized, Double-Blind, Placebo Controlled Dose-Ranging, Parallel and Adaptive Study to Evaluate the Efficacy and Safety of Enpatoran in Systemic Lupus Erythematosus and in Cutaneous ... | |||||||||||||||||||||||
Medical condition: Systemic lupus erythematosus (SLE) and cutaneous lupus erythematosus (CLE) | |||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: ES (Trial now transitioned) BG (Trial now transitioned) RO (Trial now transitioned) | |||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2021-001567-25 | Sponsor Protocol Number: ACT17010 | Start Date*: 2021-09-22 | |||||||||||
Sponsor Name:Sanofi-Aventis Recherche et Développement | |||||||||||||
Full Title: Efficacy and safety of SAR441344 in the treatment of Systemic Lupus Erythematosus: A randomized, double blind, placebo-controlled, Phase 2, proof of concept study | |||||||||||||
Medical condition: Systemic lupus erythematosus | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Ongoing) DE (Prematurely Ended) IT (Trial now transitioned) HU (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2006-003780-30 | Sponsor Protocol Number: ASF-1096-203 | Start Date*: 2006-09-05 | |||||||||||
Sponsor Name:Astion Danmark A/S | |||||||||||||
Full Title: Efficacy and safety of ASF-1096 cream 0.5 % in the treatment of patients with newly developed discoid lupus erythematosus (DLE) lesions. A multi-centre clinical phase 2, placebo controlled and doub... | |||||||||||||
Medical condition: Lupus erthematosus discoides | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2020-005569-14 | Sponsor Protocol Number: 80202135SLE2001 | Start Date*: 2021-08-24 | |||||||||||
Sponsor Name:Janssen-Cilag International NV | |||||||||||||
Full Title: A Multicenter, Randomized, Double-blind, Placebo-controlled, Parallel-group Study of Nipocalimab in Adult Participants with Active Systemic Lupus Erythematosus | |||||||||||||
Medical condition: Active Systemic Lupus Erythematosus | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: HU (Completed) PL (Completed) ES (Ongoing) BG (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2019-000638-20 | Sponsor Protocol Number: M19-130 | Start Date*: 2020-01-22 | |||||||||||
Sponsor Name:AbbVie Deutschland GmbH & Co. KG | |||||||||||||
Full Title: A Phase 2 Study to Investigate the Safety and Efficacy of Elsubrutinib and Upadacitinib Given Alone or in Combination (ABBV-599 Combination) in Subjects with Moderately to Severely Active Systemic ... | |||||||||||||
Medical condition: Systemic Lupus Erythematosus (SLE) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) ES (Completed) HU (Completed) NL (Completed) BG (Completed) IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2015-000372-95 | Sponsor Protocol Number: ALX0061-C204 | Start Date*: 2015-08-20 | |||||||||||
Sponsor Name:Ablynx N.V. | |||||||||||||
Full Title: A Phase II Multicenter, Randomized, Double-blind, Placebo controlled, Dose-range Finding Study to Evaluate the Safety and Efficacy of ALX 0061 Administered Subcutaneously in Subjects with Moderate ... | |||||||||||||
Medical condition: Moderate to Severe Active Systemic Lupus Erythematosus | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: CZ (Completed) DE (Completed) PT (Completed) HU (Completed) ES (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2010-024069-30 | Sponsor Protocol Number: CD-IA-MEDI-545-1067/D2800L00004 | Start Date*: 2011-08-05 | |||||||||||
Sponsor Name:AstraZeneca AB | |||||||||||||
Full Title: A Phase 2b, Dose-ranging Study to Evaluate the Efficacy and Safety of Sifalimumab in Adults with Systemic Lupus Erythematosus | |||||||||||||
Medical condition: Systemic Lupus Erythematosus | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Completed) GB (Completed) HU (Completed) ES (Completed) DE (Completed) IT (Completed) BG (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2015-001602-33 | Sponsor Protocol Number: RR15/114 | Start Date*: 2015-09-22 | |||||||||||
Sponsor Name:The University of Leeds | |||||||||||||
Full Title: A single arm, phase II open label trial to investigate the efficacy and safety of intra-dermal injection of etanercept for remission induction in discoid lupus erythematosus | |||||||||||||
Medical condition: Discoid lupus erythematosus | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2019-004021-25 | Sponsor Protocol Number: IM026-024 | Start Date*: 2021-10-13 | |||||||||||
Sponsor Name:Bristol-Myers Squibb International Corporation | |||||||||||||
Full Title: A Phase 2, Multicenter, Randomized, Double-blind, Placebo-Controlled, Study to Evaluate the Efficacy and Safety of BMS-986256 in Participants with Active Systemic Lupus Erythematosus. | |||||||||||||
Medical condition: Active Systemic Lupus Erythematosus. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Trial now transitioned) ES (Ongoing) PL (Trial now transitioned) IE (Trial now transitioned) RO (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2006-001062-17 | Sponsor Protocol Number: ASF-1096-201/250912BS | Start Date*: 2006-11-30 | |||||||||||
Sponsor Name:Astion Danmark A/S | |||||||||||||
Full Title: Efficacy and safety of ASF-1096 cream 0.5% in the treatment of patients with newly developed discoid lupus erythymatosus (DLE) lesions. A multi centre clinical phase 2, placebo controlled and doubl... | |||||||||||||
Medical condition: Male or female patients with a clinical diagnosis of either Discoid Lupus Erythmatosus or Systemic Lupus Erythmatosus and at least one newly developed, sharply demarcated DLE lesion. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) SE (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
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