- Trials with a EudraCT protocol (220)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
220 result(s) found for: Lupus erythematosus.
Displaying page 1 of 11.
EudraCT Number: 2005-001391-12 | Sponsor Protocol Number: TV-4710/201 | Start Date*: 2005-07-27 | |||||||||||
Sponsor Name:TEVA Pharmaceutical Industries, Ltd. | |||||||||||||
Full Title: A multi-national, multi-centre, randomized, double-blind, placebo-controlled, multiple-dose, parallel-group study to assess the efficacy, tolerability and safety of three doses of edratide (TV-4710... | |||||||||||||
Medical condition: Systemic lupus erythematosus (SLE) | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: HU (Completed) GB (Completed) ES (Completed) DE (Completed) IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2019-003409-83 | Sponsor Protocol Number: SL0046 | Start Date*: Information not available in EudraCT | |||||||||||
Sponsor Name:UCB Biopharma SRL | |||||||||||||
Full Title: A Multicenter, Open-Label Extension Study to Assess the Long-Term Safety and Tolerability of Dapirolizumab Pegol Treatment in Study Participants With Systemic Lupus Erythematosus | |||||||||||||
Medical condition: Systemic lupus erythematosus | |||||||||||||
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Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: PL (Trial now transitioned) ES (Ongoing) BG (Trial now transitioned) DE (Trial now transitioned) HU (Trial now transitioned) BE (Trial now transitioned) CZ (Trial now transitioned) GR (Trial now transitioned) FR (Trial now transitioned) IT (Trial now transitioned) AT (Prematurely Ended) DK (Trial now transitioned) RO (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2011-003814-18 | Sponsor Protocol Number: HGS1006-C1115 | Start Date*: 2012-05-03 | |||||||||||
Sponsor Name:Human Genome Sciences, Inc. (a wholly owned subsidiary of GlaxoSmithKline PLC) | |||||||||||||
Full Title: A Phase 3, Multi-Center, Randomized, Double-Blind, Placebo-Controlled, 52-Week Study to Evaluate the Efficacy and Safety of Belimumab (HGS1006) Administered Subcutaneously (SC) to Subjects with Sys... | |||||||||||||
Medical condition: Systemic lupus erythematosis (SLE) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) HU (Completed) AT (Completed) CZ (Completed) SE (Completed) BE (Completed) PT (Completed) ES (Completed) DK (Completed) GB (Completed) BG (Completed) IT (Completed) PL (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2007-007648-85 | Sponsor Protocol Number: HGS1006-C1074 | Start Date*: 2009-02-06 | |||||||||||
Sponsor Name:Human Genome Sciences, Inc. | |||||||||||||
Full Title: A Multi-Center, Continuation Trial of Belimumab (HGS1006, LymphoStat-B™), a Fully Human Monoclonal Anti-BLyS Antibody, in Subjects with Systemic Lupus Erythematosus (SLE) who Completed the Phase 3 ... | |||||||||||||
Medical condition: Systemic lupus erythematosus (SLE) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) AT (Completed) NL (Completed) BE (Completed) GB (Completed) CZ (Completed) ES (Completed) IT (Completed) SE (Completed) SK (Completed) FR (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2010-022099-29 | Sponsor Protocol Number: H9B-MC-BCDS | Start Date*: 2011-07-04 | |||||||||||
Sponsor Name:Eli Lilly and Company | |||||||||||||
Full Title: A Phase 3, Multicenter, Randomized, Double-Blind, Placebo-Controlled Study to Evaluate the Efficacy and Safety of Subcutaneous LY2127399 in Patients with Systemic Lupus Erythematosus (SLE) (ILLUMIN... | |||||||||||||
Medical condition: Systemic Lupus Erythematosus (SLE) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Prematurely Ended) AT (Completed) IT (Completed) BG (Prematurely Ended) | |||||||||||||
Trial results: View results |
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: 2019-003323-38 | Sponsor Protocol Number: J1P-MC-KFAJ | Start Date*: 2021-01-21 | |||||||||||
Sponsor Name:Eli Lilly & Company | |||||||||||||
Full Title: A Randomized, Double-Blind, Placebo-Controlled, Phase 2 Study of LY3471851 (NKTR-358) in Adults with Systemic Lupus Erythematosus | |||||||||||||
Medical condition: Systemic Lupus Erythematosus | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) HU (Completed) CZ (Completed) PL (Completed) GB (GB - no longer in EU/EEA) RO (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2021-001406-30 | Sponsor Protocol Number: J1V-MC-BT01 | Start Date*: 2022-02-02 | |||||||||||
Sponsor Name:Eli Lilly and Company | |||||||||||||
Full Title: A Multicenter, Randomized, Double-Blind, Placebo-Controlled, Parallel Group, Two Arm, Phase 2 Clinical Trial to Evaluate the Efficacy and Safety of LY3361237 to Treat Adults with At Least Moderatel... | |||||||||||||
Medical condition: Systemic Lupus Erythematosus (SLE) | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: PL (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2011-005392-16 | Sponsor Protocol Number: ORDI-03 | Start Date*: 2012-05-23 | |||||||||||
Sponsor Name:Dr Josep Ordi Ros | |||||||||||||
Full Title: Study to evaluate the efficacy and safety of Anakinra in the treatment of articular manifestations refractory to conventional therapy in Systemic Lupus Erythematosus patients | |||||||||||||
Medical condition: Systemic lupus erythematosus | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Completed) | |||||||||||||
Trial results: View results |
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: 2017-001764-37 | Sponsor Protocol Number: GA30066 | Start Date*: 2017-11-14 | |||||||||||
Sponsor Name:Genentech, Inc. | |||||||||||||
Full Title: A PHASE II, OPEN-LABEL EXTENSION STUDY OF PATIENTS PREVIOUSLY ENROLLED IN STUDY GA30044 TO EVALUATE THE LONG-TERM SAFETY AND EFFICACY OF GDC-0853 IN PATIENTS WITH MODERATE TO SEVERE ACTIVE SYSTEMI... | |||||||||||||
Medical condition: Systemic Lupus Erythematosus | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Prematurely Ended) ES (Prematurely Ended) PT (Prematurely Ended) BG (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2009-012059-47 | Sponsor Protocol Number: IFN-K-001 | Start Date*: 2010-01-28 | |||||||||||
Sponsor Name:Neovacs SA | |||||||||||||
Full Title: A phase I-II, randomized, double-blind, placebo-controlled, dose escalation study of Neovacs’ IFNα-Kinoid in adult subjects with Systemic Lupus Erythematosus. | |||||||||||||
Medical condition: Systemic Lupus Erythematosus (SLE) | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Completed) DE (Completed) FR (Completed) BG (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2025-000142-26 | Sponsor Protocol Number: 217091 | Start Date*: 2025-04-29 | |||||||||||
Sponsor Name:GlaxoSmithKline Research & Development Limited | |||||||||||||
Full Title: A Multi-Centre, Open-Label Study to Evaluate the Pharmacokinetics and Safety of Subcutaneously Administered Belimumab Plus Standard Therapy in Chinese Paediatric Participants with Systemic Lupus Er... | |||||||||||||
Medical condition: | |||||||||||||
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Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: Outside EU/EEA | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2006-006214-16 | Sponsor Protocol Number: cro967 | Start Date*: 2010-02-23 | |||||||||||
Sponsor Name:Imperial College | |||||||||||||
Full Title: A randomised placebo controlled trial of rosuvastatin in systemic lupus erythematosus. | |||||||||||||
Medical condition: Systemic lupus erythematosus. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2007-004579-21 | Sponsor Protocol Number: METc 2007/172 | Start Date*: 2007-08-27 | |||||||||||
Sponsor Name:University Medical Center Groningen | |||||||||||||
Full Title: Does booster influenza vaccination improve vaccination efficacy in patients with quiescent systemic lupus erythematosus? | |||||||||||||
Medical condition: systemic lupus erythematosus (SLE) SLE is a systemic autoimmune disease. | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2020-001690-72 | Sponsor Protocol Number: M20-186 | Start Date*: 2020-12-21 | |||||||||||
Sponsor Name:AbbVie Deutschland GmbH & Co. KG | |||||||||||||
Full Title: A Phase 2, Long-Term Extension (LTE) Study with Elsubrutinib and Upadacitinib Given Alone or in Combination (ABBV-599) in Subjects with Moderately to Severely Active Systemic Lupus Erythematosus Wh... | |||||||||||||
Medical condition: Systemic Lupus Erythematosus (SLE) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Completed) HU (Completed) DE (Completed) BG (Completed) IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2015-004404-35 | Sponsor Protocol Number: I4V-MC-JAHH | Start Date*: 2016-04-06 | |||||||||||
Sponsor Name:Eli Lilly and Company | |||||||||||||
Full Title: A Randomized, Double-Blind, Placebo-Controlled, Parallel-Group, Phase 2 Study of Baricitinib in Patients with Systemic Lupus Erythematosus (SLE) | |||||||||||||
Medical condition: Patients with Systemic Lupus Erythematosus (SLE) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: AT (Completed) PL (Completed) ES (Completed) FR (Completed) RO (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2021-006544-26 | Sponsor Protocol Number: INTONATE | Start Date*: 2022-12-23 | ||||||||||||||||
Sponsor Name:A.S.L. TO 2 | ||||||||||||||||||
Full Title: INTONATE INtensified procol for lupus nephritis with riTuximab and nO maintaiNAnce ThErapy | ||||||||||||||||||
Medical condition: lupus nephritis | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: IT (Prematurely Ended) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2010-020859-30 | Sponsor Protocol Number: SL0012 | Start Date*: 2011-05-25 | |||||||||||
Sponsor Name:UCB Inc. | |||||||||||||
Full Title: A phase 3, multicenter, open-label, extension study to asssess the safety and tolerability of Epratuzumab treatment in systemic lupus erythematosus subjects (EMBODY 4) | |||||||||||||
Medical condition: Systemic Lupus Erythematosus | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Completed) ES (Prematurely Ended) DE (Completed) CZ (Prematurely Ended) GB (Prematurely Ended) HU (Completed) BG (Prematurely Ended) LT (Prematurely Ended) IT (Completed) EE (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2014-002184-14 | Sponsor Protocol Number: IM128-027 | Start Date*: 2014-12-26 | |||||||||||
Sponsor Name:Bristol-Myers Squibb International Corporation | |||||||||||||
Full Title: A Phase 2, Multi-Center, Randomized, Double-Blind, Placebo-Controlled Study to Evaluate the Safety and Efficacy of BMS-931699 vs. Placebo on a Background of Limited Standard of care in the Treatmen... | |||||||||||||
Medical condition: Active Systemic Lupus Erythematosus | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Completed) DE (Prematurely Ended) HU (Completed) IT (Prematurely Ended) NL (Completed) | |||||||||||||
Trial results: View results |
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