- Trials with a EudraCT protocol (1,059)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
1,059 result(s) found for: Methotrexate.
Displaying page 6 of 53.
EudraCT Number: 2008-001847-20 | Sponsor Protocol Number: MA21488 | Start Date*: 2008-10-17 | |||||||||||
Sponsor Name:F Hoffmann-La Roche Ltd | |||||||||||||
Full Title: Estudio aleatorizado, controlado con placebo, para evaluar la seguridad y eficacia de añadir tocilizumab (TCZ) a metotrexato (MTX) frente al cambio a TCZ (controlado con placebo), con la posibilida... | |||||||||||||
Medical condition: Artritis reumatoide | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Completed) GB (Completed) EE (Completed) DK (Completed) FR (Completed) NL (Completed) SE (Completed) IT (Completed) LV (Completed) GR (Completed) DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2004-001236-23 | Sponsor Protocol Number: IMP 25300 | Start Date*: 2004-11-23 | |||||||||||
Sponsor Name:Serono International S.A. | |||||||||||||
Full Title: A multicentre, open label Phase IIIb/IV study of subcutaneously administered efalizumab in the treatment of adult patients with moderate to severe chronic plaque psoriasis who have failed to respon... | |||||||||||||
Medical condition: Adult patients with moderate to severe chronic plaque psoriasis who have failed to respond to, or who have a contraindication to, or are intolerant of other systemic therapies including cyclosporin... | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: HU (Completed) FI (Completed) CZ (Completed) DK (Completed) SE (Completed) ES (Completed) SK (Completed) AT (Completed) IE (Completed) IT (Completed) DE (Completed) GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2014-000358-13 | Sponsor Protocol Number: A3921187 | Start Date*: 2014-12-04 | |||||||||||
Sponsor Name:Pfizer Inc. 235 East 42nd Street, New York, NY 10017 | |||||||||||||
Full Title: A PHASE 3b/4 RANDOMIZED DOUBLE BLIND STUDY OF 5 MG OF TOFACITINIB WITH AND WITHOUT METHOTREXATE IN COMPARISON TO ADALIMUMAB WITH METHOTREXATE IN SUBJECTS WITH MODERATELY TO SEVERELY ACTIVE RHEUMATO... | |||||||||||||
Medical condition: Moderately to severely active Rheumatoid Arthritis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: CZ (Completed) EE (Completed) LT (Completed) LV (Completed) GB (Completed) ES (Completed) PL (Completed) BG (Completed) RO (Completed) DE (Completed) HR (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2008-004877-17 | Sponsor Protocol Number: RR08/8685 | Start Date*: 2011-05-12 |
Sponsor Name:University of Leeds | ||
Full Title: Prospective, Single-centre, Double-Blind, Randomised, Placebo-controlled Study Evaluating Efficacy of Adalimumab + Methotrextate Compared with Placebo + Methotrexate in Patients with Early Oligoart... | ||
Medical condition: Oligoarthritis | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (Completed) | ||
Trial results: View results |
EudraCT Number: 2009-009178-28 | Sponsor Protocol Number: UF 8469 | Start Date*: 2009-03-31 | |||||||||||
Sponsor Name:CHRU Montpellier- Direction de la Recherche, Partenariats et Réseaux, Relations avec l'Université | |||||||||||||
Full Title: Etude ouverte, randomisée, comparant l'efficacité du retraitement par etanercept ou par rituximab, après insuffisance d'efficacité du rituximab, chez les patients atteints de polyarthrite rhumatoïd... | |||||||||||||
Medical condition: acute rhumatoid polyarthritis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2010-021792-81 | Sponsor Protocol Number: 2010-12 | Start Date*: Information not available in EudraCT |
Sponsor Name:ASSISTANCE PUBLIQUE HOPITAUX DE MARSEILLE | ||
Full Title: SFCE-Metro 01 : Etude de phase II de chimiothérapie métronomique associant celecoxib-methotrexate-vinblastine-cyclophosphamide chez les enfants porteurs d’une tumeur solide en rechute ou en progre... | ||
Medical condition: children and adolescents with relapsed or progressing solid tumours. | ||
Disease: | ||
Population Age: Children, Adolescents, Under 18, Adults | Gender: Male, Female | |
Trial protocol: FR (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2008-000524-82 | Sponsor Protocol Number: RMH CCR No 3107 | Start Date*: 2008-10-09 | |||||||||||
Sponsor Name:Royal Marsden Hospital | |||||||||||||
Full Title: MESH: A Non-Randomised Phase II Trial of Methotrexate in Metastatic Colorectal Cancer with MSH2 Deficiency | |||||||||||||
Medical condition: Metastatic colorectal cancer resistanct to standard chemotherapy with evidence of deficiency of the mismatch repair gene MSH2, either on immunohistochemistry of tumour histology or on testing of pe... | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2007-004243-29 | Sponsor Protocol Number: 27809 | Start Date*: 2008-05-23 | |||||||||||
Sponsor Name:Merck Serono International SA. An Affiliate of Merck KGaA, Darmstadt, Germany | |||||||||||||
Full Title: A Phase IV open label study in moderate to severe chronic plaque psoriasis subjects transitioning from previous systemic antipsoriasis therapies (methotrexate, cyclosporine, retinoids or PUVA, NBUV... | |||||||||||||
Medical condition: Adult subjects with moderate to severe chronic plaque psoriasis who have failed to respond to, or who have a contraindication to, or are intolerant to other systemic therapies including cyclosporin... | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2019-002959-42 | Sponsor Protocol Number: 201712028 | Start Date*: 2020-01-20 |
Sponsor Name:Groupement de Coopération Sanitaire Ramsay Générale de Santé pour l’Enseignement et la Recherche | ||
Full Title: Optimization of the use of anti-TNF antibodies in Verneuil's disease: Interest of a systematic initial prescription of methotrexate | ||
Medical condition: patient suffering from Verneuil's disease: Hurley II and III stages | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: FR (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2011-001938-42 | Sponsor Protocol Number: UCL-ONCO2011-01 | Start Date*: 2012-01-24 |
Sponsor Name:Cliniques universitaires Saint-Luc | ||
Full Title: Randomized Phase II Study of CABAZITAXEL versus METHOTREXATE in patients with recurrent or metastatic squamous cell carcinoma of the head and neck previously treated with platinum-based therapy | ||
Medical condition: To evaluate the efficacy of cabazitaxel in patients with palliative head and neck previously treated with platinum-based therapy. | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: BE (Completed) | ||
Trial results: View results |
EudraCT Number: 2011-004017-17 | Sponsor Protocol Number: RR11/9965 | Start Date*: 2013-04-08 |
Sponsor Name:The University of Leeds | ||
Full Title: Prospective, Single-centre, Open-Label, Randomised, Pilot Study Assessing the changes in expression of JAK-STAT and Speed & Depth of Remission Induced by Tocilizumab & Methotrexate Combination and ... | ||
Medical condition: Rheumatoid Arthritis | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (Completed) | ||
Trial results: View results |
EudraCT Number: 2011-000391-34 | Sponsor Protocol Number: 1200.43 | Start Date*: 2011-10-25 | |||||||||||
Sponsor Name:Boehringer Ingelheim | |||||||||||||
Full Title: LUX-Head & Neck 1 A randomised, open-label, phase III study to evaluate the efficacy and safety of oral afatinib (BIBW 2992) versus intravenous methotrexate in patients with recurrent and/or metas... | |||||||||||||
Medical condition: Recurrent and/or metastatic head and neck squamous cell carcinoma in patients who have progessed after platinum based therapy | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Completed) DK (Completed) FR (Completed) DE (Completed) GR (Completed) ES (Completed) AT (Completed) CZ (Completed) SE (Completed) IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2013-002886-20 | Sponsor Protocol Number: DHNS2013-01/MOHN01 | Start Date*: 2014-01-30 |
Sponsor Name:UMC St Radboud | ||
Full Title: A phase Ib-II study of the combination of cetuximab and methotrexate in recurrent or metastatic squamous cell carcinoma of the head and neck. A study of the Dutch Head and Neck Society. | ||
Medical condition: Recurrent or metastatic squamous cell carcinoma of the head and neck (SCCHN) | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: NL (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2007-003479-37 | Sponsor Protocol Number: CER 06-167 | Start Date*: 2008-03-26 |
Sponsor Name:University Hospital of Geneva [...] | ||
Full Title: Efficacy of Methotrexate on Chronic Chondrocalcinosis | ||
Medical condition: Chronic Chondrocalcinosis | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: IE (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2005-003173-24 | Sponsor Protocol Number: AOSD Study 05 | Start Date*: 2005-12-22 |
Sponsor Name:Helsinki University Central Hospital | ||
Full Title: An open, randomized study treating refractory adult-onset Still´s disease (AOSD) with interleukin-1 receptor antagonist anakinra (KineretR), compared to an established, single anti-rheumatic drug t... | ||
Medical condition: Refractory adult onset Still´s disease (AOSD) | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: FI (Completed) SE (Ongoing) DK (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2016-000570-37 | Sponsor Protocol Number: GS-US-417-0303 | Start Date*: 2016-11-29 | |||||||||||
Sponsor Name:Gilead Sciences, Inc. | |||||||||||||
Full Title: A Randomized, Double-blind, Placebo-and Active-controlled, Multicenter, Phase 3 Study to Assess the Efficacy and Safety of Filgotinib Administered for 52 Weeks Alone and in Combination with Methotr... | |||||||||||||
Medical condition: Moderately to severely active rheumatoid arthritis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: SK (Completed) BE (Completed) GB (Completed) HU (Completed) DE (Completed) CZ (Completed) ES (Completed) PL (Completed) BG (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2009-012055-19 | Sponsor Protocol Number: ZM2009/00035/00 | Start Date*: 2010-06-16 | |||||||||||
Sponsor Name:GlaxoSmithKline Research & Development Limited | |||||||||||||
Full Title: A randomized, single-blind, placebo-controlled, parallel-group study evaluating the anti-inflammatory activity of GSK315234 in synovial biopsy tissue obtained from subjects with rheumatoid arthritis | |||||||||||||
Medical condition: Rheumatoid arthritis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IE (Prematurely Ended) BE (Completed) GB (Prematurely Ended) FR (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: 2013-004773-27 | Sponsor Protocol Number: AALL08B1 | Start Date*: 2014-03-07 | |||||||||||
Sponsor Name:Children's Oncology Group | |||||||||||||
Full Title: Classification of Newly Diagnosed Acute Lymphoblastic Leukemia (ALL) | |||||||||||||
Medical condition: Acute Lymphoblastic Leukemia | |||||||||||||
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Population Age: Infants and toddlers, Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: IE (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2009-011520-53 | Sponsor Protocol Number: ML 22508 | Start Date*: 2009-05-04 |
Sponsor Name:Roche Slovensko s.r.o. | ||
Full Title: Evaluation of Adherence and Persistence to Tocilizumab in combination with Methotrexate or Tocilizumab Monotherapy in patients with moderate to severe active rheumatoid arthritis in local environment | ||
Medical condition: moderate to severe active rheumatoid arthritis | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: SK (Completed) | ||
Trial results: View results |
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