- Trials with a EudraCT protocol (852)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
852 result(s) found for: Rheumatoid Arthritis AND Arthritis, Rheumatoid.
Displaying page 35 of 43.
EudraCT Number: 2019-000660-25 | Sponsor Protocol Number: CT-P17_3.2 | Start Date*: 2019-07-09 | |||||||||||
Sponsor Name:CELLTRION, Inc. | |||||||||||||
Full Title: A Phase III, Open-label, Single-arm, Multiple-dose Study to Evaluate Usability of Subcutaneous Auto-injector of CT-P17 in Patients with Moderate to Severe Active Rheumatoid Arthritis | |||||||||||||
Medical condition: Moderate to Severe Active Rheumatoid Arthritis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: PL (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2017-000957-37 | Sponsor Protocol Number: AS0013 | Start Date*: 2017-09-25 | |||||||||||
Sponsor Name:UCB Biopharma SRL | |||||||||||||
Full Title: A Multicenter, Phase 2A, Randomized, Investigator-Blind, Subject-Blind, Parallel-Group Study to Evaluate the Efficacy and Safety of Bimekizumab and Certolizumab Pegol in Subjects with Active Ankylo... | |||||||||||||
Medical condition: Ankylosing Spondylitis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: CZ (Completed) DE (Completed) GR (Completed) NL (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2010-023782-22 | Sponsor Protocol Number: A9391010 | Start Date*: 2011-12-16 | |||||||||||
Sponsor Name:Pfizer, S.L.U. | |||||||||||||
Full Title: A PHASE 2, RANDOMIZED, DOUBLE-BLIND ASSESSMENT OF EFFICACY AND SAFETY OF PF-04171327(1, 5, 10, 15 MG DOSE, DAILY) COMPARED TO 5 MG AND 10 MG PREDNISONE DAILY AND PLACEBO DAILY IN SUBJECTS WITH RHEU... | |||||||||||||
Medical condition: Rheumatoid Arthritis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Completed) CZ (Completed) DE (Completed) HU (Completed) SK (Completed) BG (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2014-000242-30 | Sponsor Protocol Number: CNTO148PSA3001 | Start Date*: 2014-12-29 | |||||||||||
Sponsor Name:Janssen Biologics, BV | |||||||||||||
Full Title: A Multicenter, Randomized, Double-blind, Placebo-controlled Trial of Golimumab, an Anti-TNFα Monoclonal Antibody, Administered Intravenously, in Subjects with Active Psoriatic Arthritis | |||||||||||||
Medical condition: Psoriatic Arthritis (PsA) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) LT (Completed) ES (Completed) HU (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2007-006288-56 | Sponsor Protocol Number: PROMTX2007_01 | Start Date*: 2008-05-14 |
Sponsor Name:Ludwig Boltzmann Cluster für Rheumatologie, Balneologie und Rehabilitation | ||
Full Title: Methotrexat-Polyglutamate als Marker fuer das klinische Outcome in der Therapie der rheumatoiden Arthritis | ||
Medical condition: Rheumatoid Arthritis | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: AT (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2005-000674-43 | Sponsor Protocol Number: RituxRA version1 | Start Date*: 2005-04-06 |
Sponsor Name:University of Leeds | ||
Full Title: AN OPEN LABEL STUDY OF THE EFFECT OF TREATMENT WITH RITUXIMAB ON RESISTANT RHEUMATOID ARTHRITIS: Clinical, radiological, synovial and immunological outcomes | ||
Medical condition: Rheumatoid Arthritis | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (Completed) | ||
Trial results: View results |
EudraCT Number: 2006-002748-27 | Sponsor Protocol Number: 0881A3-403 | Start Date*: 2007-04-13 | |||||||||||
Sponsor Name:Wyeth Pharmaceuticals France | |||||||||||||
Full Title: A Multicentre, Double-Blind, Placebo-Controlled, Randomised Study of Etanercept in the Treatment of Adult Patients with Active, Severe and Advanced Axial Ankylosing Spondylitis | |||||||||||||
Medical condition: Active, severe and advanced axial ankylosing spondylitis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Completed) DE (Completed) FR (Completed) HU (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2012-001171-37 | Sponsor Protocol Number: 20021626 | Start Date*: 2012-03-07 |
Sponsor Name:Amgen, Inc. One Amgen Center Drive Thousand Oaks, California 91320 | ||
Full Title: A Phase IV Registry of Etanercept in Children With Juvenile Rheumatoid Arthritis | ||
Medical condition: Juvenile idiopathic arthritis (JIA) | ||
Disease: | ||
Population Age: Infants and toddlers, Children, Adolescents, Under 18, Adults | Gender: Male, Female | |
Trial protocol: Outside EU/EEA | ||
Trial results: View results |
EudraCT Number: 2016-002035-15 | Sponsor Protocol Number: 0 | Start Date*: 2016-05-20 | ||||||||||||||||
Sponsor Name:Helsinki University Central Hospital | ||||||||||||||||||
Full Title: Outcome after total knee arthroplasty under general or spinal anesthesia, a randomized study | ||||||||||||||||||
Medical condition: Patients undego total knee arthroplasty operation in general or spinal anaesthesia because of osteoarthritis, rheumatoid arthritis or other degenerative condition of the knee | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: FI (Completed) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2015-000570-35 | Sponsor Protocol Number: 01-2015 | Start Date*: 2016-02-10 | |||||||||||||||||||||
Sponsor Name:DIPARTIMENTO DI MEDICINA CLINICA E CHIRURGIA - UNIVERSITÀ DEGLI STUDI DI NAPOLI FEDERICO II | |||||||||||||||||||||||
Full Title: Prophylaxis of Hepatitis B reactivation in patients with HBV occult infection and rheumatological diseases candidates to immune suppressive treatments of finite duration. | |||||||||||||||||||||||
Medical condition: Occult Hepatitis B virus Infection (OBI) in patients with rheumatologic diseases candidate to treatment a finite duration (less than 18 months) with potent immune suppressive drugs | |||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: IT (Prematurely Ended) | |||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2016-002958-21 | Sponsor Protocol Number: HCV-art | Start Date*: 2017-05-16 | ||||||||||||||||
Sponsor Name:AOU DI BOLOGNA POLICLINICO S.ORSOLA-MALPIGHI | ||||||||||||||||||
Full Title: Study HCV-art: An Open-Label, pilot Study, to Explore the Clinical Safety and Efficacy of Sofosbuvir/Ledipasvir in Hepatitis C Virus (HCV) Chronic Patients with Arthritis | ||||||||||||||||||
Medical condition: Chronic HCV associated with chronic arthritis. | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: IT (Prematurely Ended) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2016-001163-37 | Sponsor Protocol Number: CNTO1959PSA3001 | Start Date*: 2017-07-25 | |||||||||||
Sponsor Name:Janssen-Cilag International N.V. | |||||||||||||
Full Title: A Phase 3, Multicenter, Randomized, Double-blind, Placebo-controlled Study Evaluating the Efficacy and Safety of Guselkumab Administered Subcutaneously in Subjects with Active Psoriatic Arthritis i... | |||||||||||||
Medical condition: Active Psoriatic Arthritis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: HU (Completed) CZ (Completed) ES (Completed) DE (Completed) PL (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2009-012118-27 | Sponsor Protocol Number: 38518168ARA2001 | Start Date*: 2009-10-27 | |||||||||||
Sponsor Name:Janssen-Cilag International NV | |||||||||||||
Full Title: A Phase IIa Multicenter, Randomized, Double-Blind, Placebo-Controlled, Parallel Group Study of JNJ-38518168 in Subjects with Active Rheumatoid Arthritis Despite Methotrexate Therapy With Synovial B... | |||||||||||||
Medical condition: JNJ-38518168 is being developed for the treatment of Rheumatoid Arthritis. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Prematurely Ended) GB (Prematurely Ended) CZ (Prematurely Ended) ES (Prematurely Ended) BE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2012-004090-16 | Sponsor Protocol Number: 1293.2 | Start Date*: 2013-04-23 |
Sponsor Name:Boehringer Ingelheim Pharma GmbH & Co. KG | ||
Full Title: A randomised, double-blind, placebo-controlled trial for establishing safety, tolerability, pharmacokinetics, pharmacodynamics and clinical efficacy of multiple subcutaneous doses of BI 655064 in h... | ||
Medical condition: Rheumatoid arthritis | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: DE (Completed) ES (Completed) CZ (Completed) NL (Completed) | ||
Trial results: View results |
EudraCT Number: 2007-006539-29 | Sponsor Protocol Number: 0 | Start Date*: 2008-03-14 |
Sponsor Name:Dept of Rheumatology, Lund University Hospital, Lund, Sweden | ||
Full Title: Effects of different anti-rheumatic treatments of arthritis on antibody response following pneumococcal vaccination using Prevenar | ||
Medical condition: Patients with rheumatic diseases (rheumatoid arthritis and spondyloarthripaties) who are going to be vaccinated with Prevenar vaccine in order to study the serological responses to two pneumococc... | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: SE (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2015-000050-38 | Sponsor Protocol Number: CAIN457F2342 | Start Date*: 2015-07-07 | |||||||||||
Sponsor Name:Novartis Pharma Services AG | |||||||||||||
Full Title: A Phase III, randomized, double-blind, placebo controlled multi-center study of subcutaneous secukinumab (150 mg and 300 mg) in prefilled syringe to demonstrate efficacy (including inhibition of st... | |||||||||||||
Medical condition: Psoriatic Arthritis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: LT (Completed) IE (Completed) HU (Completed) NL (Completed) ES (Completed) DE (Completed) IT (Completed) AT (Completed) LV (Completed) DK (Completed) CZ (Completed) FI (Completed) EE (Completed) GR (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2016-000568-41 | Sponsor Protocol Number: GS-US-417-0301 | Start Date*: 2016-10-11 | |||||||||||
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 in Combination with Methotrexate to ... | |||||||||||||
Medical condition: Moderately to severely active rheumatoid arthritis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: SK (Completed) GB (Completed) BE (Completed) HU (Completed) CZ (Completed) DE (Completed) ES (Completed) BG (Completed) PL (Completed) NL (Completed) IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2007-006729-28 | Sponsor Protocol Number: Not applicable | Start Date*: 2008-01-25 | |||||||||||
Sponsor Name:Trafford NHS Trust | |||||||||||||
Full Title: Is a single dose intramuscular (IM) triamcinolone acetonide injection more effective in treating symptomatic flare in established rheumatoid arthritis than equivalent dose of oral prednisolone? | |||||||||||||
Medical condition: The objective of this study is to compare the efficacy of equivalent doses of IM triamcinolone acetonide and oral prednisolone in controlling a symptomatic flare in patients with established RA. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2014-005418-45 | Sponsor Protocol Number: HCQCVDRASLE-1.1 | Start Date*: 2015-05-04 |
Sponsor Name:Christine Bengtsson [...] | ||
Full Title: Improved cardiovascular risk factors and inflammatory markers in Rheumatoid Arthritis and Systemic Lupus Erythematosus? New aspects of Hydroxychloroquine – an interventional study (HCQCVDRASLE) | ||
Medical condition: Rheumatoid Arthritis and Systemic Lupus Erythematosus | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: SE (Completed) | ||
Trial results: View results |
EudraCT Number: 2011-002067-20 | Sponsor Protocol Number: RA0077 | Start Date*: 2012-06-13 | |||||||||||
Sponsor Name:UCB Pharma SA | |||||||||||||
Full Title: A multicenter, single blind, randomized parallel group study to assess the short and long term efficacy of certolizumab pegol plus methotrexate compared with adalimumab plus methotrexate in subject... | |||||||||||||
Medical condition: Moderate to severe rheumatoid arthritis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) GB (Completed) HU (Completed) PT (Completed) AT (Completed) IE (Completed) CZ (Completed) ES (Completed) BG (Completed) FR (Completed) IT (Completed) GR (Prematurely Ended) | |||||||||||||
Trial results: View results |
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