- Trials with a EudraCT protocol (613)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
613 result(s) found for: Active Rheumatoid Arthritis AND Arthritis.
Displaying page 7 of 31.
EudraCT Number: 2007-003591-19 | Sponsor Protocol Number: MC-MTX.10/RH | Start Date*: Information not available in EudraCT | |||||||||||
Sponsor Name:medac Gesellschaft für klinische Spezialpräparate mbH | |||||||||||||
Full Title: AN OPEN, COMPARATIVE, WITHIN PATIENT CONTROLLED MULTICENTRE STUDY OF REPEATED SUBCUTANEOUS INJECTIONS OF METHOTREXATE 50MG/ML AND 10MG/ML TO COMPARE PATIENT SATISFACTION AND LOCAL TOLERABILITY IN P... | |||||||||||||
Medical condition: Rheumatoid arthritis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2010-019964-36 | Sponsor Protocol Number: CL004_354 | Start Date*: 2010-08-26 | |||||||||||
Sponsor Name:ChemoCentryx, Inc. | |||||||||||||
Full Title: A Randomized, Double-Blind, Placebo-Controlled, Phase 2 Study to Evaluate the Safety and Efficacy of CCX354-C in Subjects with Rheumatoid Arthritis Partially Responsive to Methotrexate Therapy | |||||||||||||
Medical condition: Rheumatoid arthritis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Completed) HU (Completed) CZ (Completed) DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2009-011206-42 | Sponsor Protocol Number: INCB 28050-201 | Start Date*: 2009-08-18 | |||||||||||
Sponsor Name:Incyte Corporation | |||||||||||||
Full Title: A Randomized, Double Blind, Placebo Controlled, Dose Ranging, Parallel Group, Phase 2 Study of INCB028050 Compared to Background Therapy in Patients with Active Rheumatoid Arthritis with Inadequate... | |||||||||||||
Medical condition: Active Rheumatoid Arthritis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: CZ (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2008-006930-92 | Sponsor Protocol Number: ART621-221 | Start Date*: 2009-03-31 | |||||||||||
Sponsor Name:Arana Therapeutics Ltd | |||||||||||||
Full Title: A multi-centre randomised, double-blind, placebo-controlled, dose-ranging study to evaluate the safety, tolerability, efficacy, pharmacokinetics and immunogenicity of ART621 following multiple dose... | |||||||||||||
Medical condition: Rheumatoid arthritis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: CZ (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2021-004031-86 | Sponsor Protocol Number: CEST-JIA | Start Date*: 2021-12-21 | ||||||||||||||||||||||||||
Sponsor Name:FONDAZIONE IRCCS CA' GRANDA OSPEDALE MAGGIORE POLICLINICO | ||||||||||||||||||||||||||||
Full Title: “A randomized, two-armed, single-blind, parallel, active controlled, and non-inferiority clinical trial to Compare Efficacy and Safety of anti TNF-alfa biosimilar molecules to the originators in ch... | ||||||||||||||||||||||||||||
Medical condition: Juvenile Idiopathic Arthritis | ||||||||||||||||||||||||||||
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Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | |||||||||||||||||||||||||||
Trial protocol: IT (Trial now transitioned) | ||||||||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2015-002634-41 | Sponsor Protocol Number: 1297.3 | Start Date*: 2016-01-07 | |||||||||||
Sponsor Name:Boehringer Ingelheim International GmbH | |||||||||||||
Full Title: Long-term assessment of safety, efficacy, pharmacokinetics and immunogenicity of BI 695501 in patients with rheumatoid arthritis (RA): an open-label extension trial for patients who have completed ... | |||||||||||||
Medical condition: Rheumatoid arthritis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: HU (Completed) ES (Completed) DE (Completed) PL (Completed) BG (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2009-012185-32 | Sponsor Protocol Number: ML22413 | Start Date*: 2009-11-23 | |||||||||||
Sponsor Name:ROCHE | |||||||||||||
Full Title: Open label, multicentric phase IIIb study to evaluate the effect of tocilizumab in combination with DMARDs in the inhibition of progression of synovitis, bone marrow edema, and erosions evaluated b... | |||||||||||||
Medical condition: Moderate to severe active rheumatoid arthritis (RA), who are inadequate responders to DMARDs. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2007-003069-42 | Sponsor Protocol Number: CRx-102-007 | Start Date*: 2007-10-31 | |||||||||||
Sponsor Name:CombinatoRx, Incorporated | |||||||||||||
Full Title: A RANDOMIZED, DOUBLE-BLIND, PLACEBO-CONTROLLED, MULTI-CENTER STUDY TO EVALUATE THE SUPERIORITY OF CRX-102 OVER EACH OF ITS COMPONENTS WHEN GIVEN TO SUBJECTS WITH ACTIVE RHEUMATOID ARTHRITIS (RA) | |||||||||||||
Medical condition: RHEUMATOID ARTHRITIS (RA) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: EE (Prematurely Ended) GB (Prematurely Ended) HU (Completed) LT (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2010-018331-18 | Sponsor Protocol Number: ML25243 | Start Date*: 2010-05-12 | |||||||||||
Sponsor Name:F. Hoffmann-La Roche Ltd. | |||||||||||||
Full Title: A 52 week, Single center, Open-label Study to Evaluate Neutrophil function and survival effects of Tocilizumab (TCZ) in Patients with Active Rheumatoid Arthritis (RA) on Background Non-biologic DMA... | |||||||||||||
Medical condition: Adult Rheumatoid Arthritis (RA) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2021-006007-15 | Sponsor Protocol Number: JAKAR | Start Date*: 2022-09-01 | |||||||||||
Sponsor Name:Leiden University Medical Center (LUMC) | |||||||||||||
Full Title: Januse kinase Inhibition with Filgotinib to Silence Autoreactive B cells in Rheumatoid Arthritis | |||||||||||||
Medical condition: patients with ACPA-positieve active RA | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2007-002950-42 | Sponsor Protocol Number: GEN410/OFA110635 | Start Date*: 2007-10-18 | |||||||||||
Sponsor Name:Genmab A/S | |||||||||||||
Full Title: A double-blind, randomized, placebo controlled, parallel group, multi-center, phase III trial of ofatumumab investigating clinical efficacy in adult patients with active rheumatoid arthritis who ha... | |||||||||||||
Medical condition: Rheumatoid Arthritis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: HU (Completed) LT (Prematurely Ended) CZ (Completed) PL (Completed) ES (Completed) GB (Completed) BE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2009-012424-87 | Sponsor Protocol Number: 2104091 | Start Date*: 2009-11-26 | |||||||||||||||||||||
Sponsor Name:Imperial College London South Kensington London | |||||||||||||||||||||||
Full Title: T cells and TNF: The impct of TNF blockade on effector T cell populations in rheumatoid arthritis and other conditions treated with anti-TNF-alpha agents. | |||||||||||||||||||||||
Medical condition: Rheumatoid arthritis Psoriatic arthritis Ankylosing spondylitis | |||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: GB (Completed) | |||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2012-002339-27 | Sponsor Protocol Number: I4V-MC-JADX | Start Date*: 2013-01-14 | |||||||||||
Sponsor Name:Eli Lilly and Company | |||||||||||||
Full Title: A Randomized, Double-Blind, Placebo-Controlled, Phase 3 Study to Evaluate the Efficacy and Safety of Baricitinib (LY3009104) in Patients with Inadequate Response to Conventional Disease-Modifying A... | |||||||||||||
Medical condition: Moderately to severely active rheumatoid arthritis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: HU (Completed) BE (Completed) DE (Completed) IT (Completed) PT (Completed) GB (Completed) CZ (Completed) SK (Completed) ES (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2004-004022-27 | Sponsor Protocol Number: WA18155 | Start Date*: 2005-03-24 | |||||||||||
Sponsor Name:F.Hoffmann - La Roche Ltd | |||||||||||||
Full Title: Phase IIa, multicenter, randomised, double-blind, placebo controlled study of the efficacy and safety of RO0506997, an α4 integrin antagonist, in combination with methotrexate, versus methotrexate ... | |||||||||||||
Medical condition: Rhematoid Arthritis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2015-000089-72 | Sponsor Protocol Number: 204 | Start Date*: 2015-03-26 | |||||||||||
Sponsor Name:Policlinico Gemelli-CIC- UCSC | |||||||||||||
Full Title: FAT GENE EXPRESSION IN OVERWEIGHT AND OBESE PATIENTS WITH PERSISTENTLY ACTIVE RHEUMATOID ARTHRITIS TREATED WITH ABATACEPT AND CLINICAL RESPONSE | |||||||||||||
Medical condition: | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2009-017306-36 | Sponsor Protocol Number: TIGER | Start Date*: 2010-11-19 | |||||||||||
Sponsor Name:Leiden University Medical Center, Department of Rheumatology | |||||||||||||
Full Title: ANTI-IGE THERAPY (OMALIZUMAB) IN IGE-ACPA POSITIVE RA. | |||||||||||||
Medical condition: RHEUMATOID ARTHRITIS | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2006-003142-42 | Sponsor Protocol Number: SC12267-3-2005 | Start Date*: 2006-11-30 | |||||||||||
Sponsor Name:4SC AG | |||||||||||||
Full Title: A Randomized, Double Blind, Placebo-controlled, Proof of Concept Study to evaluate Efficacy, Safety and Pharmacokinetics of two Different Doses of SC12267 (20mg, 35 mg) in Patients with Rheumatoid ... | |||||||||||||
Medical condition: Active Rheumatoid Arthritis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2012-000535-36 | Sponsor Protocol Number: M13-390 | Start Date*: 2012-08-28 | |||||||||||
Sponsor Name:Abbott GmbH & Co. KG | |||||||||||||
Full Title: A multicenter, randomized, double-blind, double dummy, parallel design study to assess pharmacokinetic, pharmacodynamic, safety and immunogenicity of a new adalimumab formulation compared to the cu... | |||||||||||||
Medical condition: Rheumatoid Arthritis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Prematurely Ended) SK (Completed) DE (Completed) CZ (Completed) PL (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2005-002629-30 | Sponsor Protocol Number: CDP870-051 | Start Date*: 2006-01-30 | |||||||||||
Sponsor Name:UCB Inc | |||||||||||||
Full Title: A Phase III Multi-center, Open-label, Follow-up Study, to Assess the Safety and Efficacy of Liquid Certolizumab Pegol as Additional Medication to Methotrexate, in the Treatment of Signs and Symptom... | |||||||||||||
Medical condition: Rheumatoid arthritis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: LT (Completed) SK (Completed) CZ (Completed) EE (Completed) LV (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2010-022378-15 | Sponsor Protocol Number: VT-4001-001-SP | Start Date*: 2011-05-25 | |||||||||||
Sponsor Name:Nycomed GmbH | |||||||||||||
Full Title: VELVET (Veltuzumab various doses exploratory trial), a randomized, double blind, placebo controlled, multicentre, multinational phase II dose range finding trial in subjects with moderate to severe... | |||||||||||||
Medical condition: Rheumatoid arthritis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Prematurely Ended) GB (Prematurely Ended) ES (Prematurely Ended) CZ (Prematurely Ended) HU (Prematurely Ended) | |||||||||||||
Trial results: View results |
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