- 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 1 of 31.
EudraCT Number: 2009-017325-19 | Sponsor Protocol Number: FI-08-03 | Start Date*: 2010-02-11 | ||||||||||||||||||||||||||
Sponsor Name:Helsingin reumakeskus | ||||||||||||||||||||||||||||
Full Title: “The effect of Six months Adalimumab Treatment on Sick Leaves and retirement in Patients with rheumatoid Arthritis who are at risk of losing their ability to work” | ||||||||||||||||||||||||||||
Medical condition: Rheumatoid arthritis | ||||||||||||||||||||||||||||
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Population Age: Adults | Gender: Male, Female | |||||||||||||||||||||||||||
Trial protocol: FI (Completed) | ||||||||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2010-023469-22 | Sponsor Protocol Number: P10.YYY/ APCP-107 | Start Date*: 2011-03-09 | ||||||||||||||||
Sponsor Name:LUMC | ||||||||||||||||||
Full Title: A phase II study of ARA 290 as therapeutic strategy in rheumatoid arthritis | ||||||||||||||||||
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: 2010-019262-86 | Sponsor Protocol Number: LTS11210 | Start Date*: 2011-06-22 | |||||||||||
Sponsor Name:sanofi-aventis Recherche & Développement | |||||||||||||
Full Title: Estudio de extensión multicéntrico no controlado que evalúa la eficacia y seguridad de SAR153191 junto con Fármacos Anti-Reumáticos Modificadores de la Enfermedad (FARMEs) en pacientes con Artritis... | |||||||||||||
Medical condition: Artritis Reumatoide _______________________ Rheumatoid Arthritis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Completed) FI (Completed) EE (Completed) HU (Completed) NL (Completed) DE (Completed) GR (Completed) NO (Completed) LT (Completed) CZ (Completed) IT (Completed) AT (Completed) PT (Completed) SK (Completed) GB (GB - no longer in EU/EEA) BE (Completed) SE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2008-000587-17 | Sponsor Protocol Number: MA21573 | Start Date*: 2008-06-18 | |||||||||||
Sponsor Name:F. Hoffmann-La Roche Ltd | |||||||||||||
Full Title: Multi-National Open-Label Study to Evaluate the Safety, Tolerability and Efficacy of Tocilizumab in Patients with Active Rheumatoid Arthritis on Background Non-biologic DMARDs who have an Inadequat... | |||||||||||||
Medical condition: Rheumatoid arthritis. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) AT (Completed) SE (Completed) ES (Completed) FI (Completed) IE (Completed) PT (Completed) CZ (Completed) DK (Completed) FR (Completed) BE (Completed) NL (Completed) HU (Completed) DE (Completed) GR (Completed) IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2006-005386-19 | Sponsor Protocol Number: Anti TNF resistant RA / RTX / mini | Start Date*: 2006-12-19 | |||||||||||
Sponsor Name:Cliniques Universitaires Saint-Luc | |||||||||||||
Full Title: Cytokines and inflammatory proteins gene expression study in synovial biopsies from rheumatoid arthritis patients refractory to anti-TNF therapy treated with Rituximab | |||||||||||||
Medical condition: Rheumatoid arthritis refractory to TNF blockers patients | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2007-000491-16 | Sponsor Protocol Number: CACZ885A2201E1 | Start Date*: 2007-04-30 | |||||||||||
Sponsor Name:Novartis Farmacéutica, S.A. | |||||||||||||
Full Title: Estudio de extensión abierto de 76 semanas de duración para evaluar la eficacia, seguridad y tolerabilidad de ACZ885 (anticuerpo monoclonal anti-interleuquina-1β) en pacientes con artritis reumatoi... | |||||||||||||
Medical condition: Artritis Reumatoide | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Completed) DE (Prematurely Ended) AT (Completed) BE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2007-006527-13 | Sponsor Protocol Number: CF101-203RA | Start Date*: 2008-06-18 | ||||||||||||||||
Sponsor Name:Can-Fite BioPharma Ltd. | ||||||||||||||||||
Full Title: A Phase 2, Multicenter, Randomized, Double-Blind, Placebo-Controlled, Parallel-Group, Dose-Finding Study of the Safety and Efficacy of Daily CF101 Administered Orally, When Added to Weekly Methotre... | ||||||||||||||||||
Medical condition: Rheumatoid Arthritis | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: BG (Prohibited by CA) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2006-005391-40 | Sponsor Protocol Number: PRPINAR2006 | Start Date*: 2006-09-25 | |||||||||||
Sponsor Name:AZIENDA OSPEDALIERA SENESE | |||||||||||||
Full Title: Study on the effect of intra-articular infiltrations of aulogous platelet gel as inhibitor of erosion in rheumatoid arthritis patients | |||||||||||||
Medical condition: Patients with Rheumatoid Arthritis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2011-005648-93 | Sponsor Protocol Number: CD-IA-CAM-3001-1109 | Start Date*: 2012-07-19 | |||||||||||
Sponsor Name:MedImmune Ltd | |||||||||||||
Full Title: An Open-label Extension Study to Evaluate the Long-term Safety of Mavrilimumab in Adult Subjects with Rheumatoid Arthritis | |||||||||||||
Medical condition: Rheumatoid arthritis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: EE (Completed) HU (Completed) CZ (Completed) DE (Completed) ES (Completed) BG (Completed) GR (Completed) SK (Completed) PT (Completed) GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2010-020892-22 | Sponsor Protocol Number: D4300C00005 | Start Date*: 2010-11-23 | |||||||||||
Sponsor Name:AstraZeneca AB | |||||||||||||
Full Title: A Long-term Extension Study to Assess the Safety and Efficacy of Fostamatinib Disodium (FosD) in the Treatment of Rheumatoid Arthritis | |||||||||||||
Medical condition: Rheumatoid Arthritis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Prematurely Ended) GB (Prematurely Ended) DE (Completed) SK (Prematurely Ended) HU (Prematurely Ended) LV (Prematurely Ended) EE (Prematurely Ended) LT (Prematurely Ended) CZ (Prematurely Ended) PT (Prematurely Ended) ES (Prematurely Ended) BG (Prematurely Ended) IT (Prematurely Ended) NL (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2008-006924-68 | Sponsor Protocol Number: MA22460 | Start Date*: 2010-10-28 | |||||||||||
Sponsor Name:F. Hoffmann-La Roche Ltd | |||||||||||||
Full Title: Extension Phase of the Multi-National Open-Label Study to Evaluate the Safety, Tolerability and Efficacy of Tocilizumab in Patients with Active Rheumatoid Arthritis on Background Non-biologic DMARD... | |||||||||||||
Medical condition: Rheumatoid arthritis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: AT (Prematurely Ended) ES (Completed) NL (Completed) CZ (Completed) PT (Completed) FR (Completed) IT (Completed) GB (Completed) HU (Completed) GR (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2009-016266-90 | Sponsor Protocol Number: EFC11072 | Start Date*: 2011-05-03 | |||||||||||
Sponsor Name:Sanofi-aventis Recherche & Développement | |||||||||||||
Full Title: Estudio aleatorizado, doble-ciego, controlado con placebo, multicéntrico, de dos partes, de búsqueda de dosis y confirmatorio, con un diseño operacionalmente adaptativo que evalúa la eficacia y seg... | |||||||||||||
Medical condition: Artritis Reumatoide _____________________________________ Rheumatoid Arthritis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Completed) CZ (Completed) FI (Completed) HU (Completed) EE (Completed) DE (Completed) LT (Completed) PT (Completed) NL (Completed) GR (Completed) RO (Completed) AT (Completed) BE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2009-012759-12 | Sponsor Protocol Number: WA19926 | Start Date*: 2009-10-14 | |||||||||||
Sponsor Name:F. Hoffmann-La Roche Ltd. | |||||||||||||
Full Title: A multi-center, randomized, double-blind, parallel group study of the safety, disease remission and prevention of structural joint damage during treatment with tocilizumab (TCZ), as a monotherapy a... | |||||||||||||
Medical condition: Rheumatoid Arthritis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) AT (Completed) DE (Completed) ES (Completed) FI (Completed) FR (Completed) PT (Completed) DK (Completed) IE (Completed) GR (Completed) SE (Completed) IT (Completed) HU (Completed) CZ (Completed) | |||||||||||||
Trial results: Removed from public view |
EudraCT Number: 2011-005634-19 | Sponsor Protocol Number: CD-IA-CAM-3001-1071 | Start Date*: 2012-05-30 | |||||||||||
Sponsor Name:MedImmune Ltd | |||||||||||||
Full Title: A Phase 2b Study to Evaluate the Efficacy and Safety of Mavrilimumab in Subjects with Moderate-to-Severe Rheumatoid Arthritis. | |||||||||||||
Medical condition: Rheumatoid arthritis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: HU (Completed) EE (Completed) CZ (Completed) ES (Completed) DE (Completed) BG (Completed) PL (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2004-002993-49 | Sponsor Protocol Number: CDP870-027 | Start Date*: 2005-02-11 | |||||||||||
Sponsor Name:Celltech R&D Ltd | |||||||||||||
Full Title: A Phase III multicentre, double blind, placebo-controlled, parallel group 52-week study to assess the efficacy and safety of 2 dose regimens of lyophilised CDP870 given subcutaneously as additional... | |||||||||||||
Medical condition: Rheumatoid Arthritis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: HU (Completed) FI (Completed) LT (Completed) SE (Completed) SK (Completed) CZ (Completed) EE (Completed) LV (Completed) BE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2020-002673-10 | Sponsor Protocol Number: J1A-MC-KDAD | Start Date*: 2021-02-17 | |||||||||||
Sponsor Name:Eli Lilly and Company | |||||||||||||
Full Title: A Phase 2 Study to Evaluate the Efficacy and Safety of LY3462817 in Participants with Moderately to Severely Active Rheumatoid Arthritis | |||||||||||||
Medical condition: Moderately to Severely Active Rheumatoid Arthritis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: CZ (Completed) HU (Completed) PL (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2016-002852-26 | Sponsor Protocol Number: MS200588-0004 | Start Date*: 2016-12-07 | |||||||||||
Sponsor Name:Merck KGaA | |||||||||||||
Full Title: A multicenter, randomized, double-blind, Phase III trial to evaluate the safety, immunogenicity, and efficacy of MSB11022 compared with Humira® in patients with moderately to severely active rheuma... | |||||||||||||
Medical condition: moderately to severely active rheumatoid arthritis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: CZ (Completed) GB (Completed) HU (Completed) DE (Completed) LT (Prematurely Ended) BG (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2016-000933-37 | Sponsor Protocol Number: M15-925 | Start Date*: 2016-11-24 | |||||||||||
Sponsor Name:AbbVie Deutschland GmbH & Co. KG | |||||||||||||
Full Title: A Phase 3, Randomized, Active-Controlled, Double Blind Study Comparing Upadacitinib to Abatacept in Subjects with Moderately to Severely Active Rheumatoid Arthritis with Inadequate Response or Into... | |||||||||||||
Medical condition: Moderately to Severely Active Rheumatoid Arthritis (RA) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: HU (Completed) DE (Completed) LV (Completed) PT (Completed) SE (Completed) ES (Ongoing) CZ (Completed) BE (Completed) NL (Completed) SK (Prematurely Ended) BG (Completed) IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2011-003538-16 | Sponsor Protocol Number: EFC10832 | Start Date*: 2013-02-04 | |||||||||||
Sponsor Name:sanofi-aventis recherche & développement | |||||||||||||
Full Title: A Randomized, Double-blind, Parallel, Placebo-controlled Study Assessing The Efficacy and Safety of Sarilumab Added To non-biologic DMARD Therapy In Patients With Rheumatoid Arthritis Who Are Inade... | |||||||||||||
Medical condition: Rheumatoid Arthritis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: LT (Completed) CZ (Completed) HU (Completed) ES (Completed) DE (Completed) PT (Completed) GR (Completed) AT (Completed) IT (Completed) SK (Completed) PL (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2006-003054-26 | Sponsor Protocol Number: TAK-783/EC201 | Start Date*: 2007-08-31 | |||||||||||
Sponsor Name:Takeda Global R&D (Europe) Ltd | |||||||||||||
Full Title: A Randomized, Double-Blind, Placebo-Controlled Proof of Concept Study to Evaluate the Safety and Efficacy of Oral TAK-783 in the Treatment of the Signs and Symptoms of in Subjects with Rheumatoid A... | |||||||||||||
Medical condition: Rheumatoid arthritis (RA) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: CZ (Completed) LV (Completed) HU (Prematurely Ended) | |||||||||||||
Trial results: View results |
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