- Trials with a EudraCT protocol (436)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
436 result(s) found for: MabThera (rituximab).
Displaying page 6 of 22.
EudraCT Number: 2006-005552-33 | Sponsor Protocol Number: APO3585g | Start Date*: 2007-06-06 | |||||||||||
Sponsor Name:Genentech Inc. | |||||||||||||
Full Title: A PHASE Ib/II, OPEN-LABEL, MULTICENTER STUDY OF THE SAFETY, PHARMACOKINETICS, AND EFFICACY OF Apo2L/TRAIL ADMINISTERED INTRAVENOUSLY IN COMBINATION WITH RITUXIMAB TO SUBJECTS WITH FOLLICULAR AND OT... | |||||||||||||
Medical condition: Follicular, CD20+, B-cell non-Hodgkin’s lymphoma. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Completed) CZ (Prematurely Ended) IT (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2016-000209-35 | Sponsor Protocol Number: 7805 | Start Date*: 2016-08-24 |
Sponsor Name:Newcastle upon Tyne Hospitals NHS Foundation Trust | ||
Full Title: Adjuvant rituximab – a potential treatment for the young patient with Graves’ hyperthyroidism | ||
Medical condition: Graves' hyperthyroidism | ||
Disease: | ||
Population Age: Adolescents, Under 18, Adults | Gender: Male, Female | |
Trial protocol: GB (Completed) | ||
Trial results: View results |
EudraCT Number: 2016-000211-33 | Sponsor Protocol Number: P02100 | Start Date*: 2016-10-06 | |||||||||||
Sponsor Name:Papworth Hospital NHS Foundation Trust | |||||||||||||
Full Title: Dose Effect Relationship of a Single Dose of Rituximab on the Kinetics of B Lymphocytes in Patients with Acute ST-Segment Myocardial Infarction | |||||||||||||
Medical condition: Anterior STEMI revascularised by PPCI | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2013-002110-12 | Sponsor Protocol Number: GO28667 | Start Date*: 2014-02-26 | |||||||||||
Sponsor Name:AbbVie Deutschland GmbH & Co. KG | |||||||||||||
Full Title: A MULTICENTER, PHASE III, OPEN-LABEL, RANDOMIZED STUDY IN RELAPSED/REFRACTORY PATIENTS WITH CHRONIC LYMPHOCYTIC LEUKEMIA TO EVALUATE THE BENEFIT OF GDC-0199 (ABT-199) PLUS RITUXIMAB COMPARED WITH... | |||||||||||||
Medical condition: Relapsed/Refractory Chronic Lymphocytic Leukemia (CLL) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: CZ (Completed) SE (Completed) BE (Completed) GB (GB - no longer in EU/EEA) AT (Completed) IT (Completed) FR (Completed) NL (Completed) HU (Completed) DK (Completed) DE (Completed) ES (Completed) PL (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2013-004341-17 | Sponsor Protocol Number: PCYC-1123-CA | Start Date*: 2014-10-16 | |||||||||||
Sponsor Name:Pharmacyclics LLC | |||||||||||||
Full Title: A Multicenter Open-Label Phase 1b/2 Study of the Bruton’s Tyrosine Kinase (BTK) Inhibitor, Ibrutinib, in Combination with Lenalidomide and Rituximab in Subjects with Relapsed or Refractory Diffuse... | |||||||||||||
Medical condition: Relapsed or Refractory Diffuse Large B-Cell Lymphoma | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Completed) GB (GB - no longer in EU/EEA) | |||||||||||||
Trial results: View results |
EudraCT Number: 2013-005543-90 | Sponsor Protocol Number: 20130108 | Start Date*: 2014-08-26 | |||||||||||
Sponsor Name:Amgen Inc | |||||||||||||
Full Title: A Randomized, Double-Blind Study to Compare Pharmacokinetics and Pharmacodynamics, Efficacy and Safety of ABP 798 With Rituximab 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) DE (Completed) PL (Completed) BG (Completed) EE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2018-004619-28 | Sponsor Protocol Number: RITS-PO-2019 | Start Date*: 2019-04-24 |
Sponsor Name:Region Örebro län | ||
Full Title: Rituximab - Immunotherapy for Obsessive-Compulsive Disorder. An open pilot study. | ||
Medical condition: Treatment-resistant patients with Obsessive Compulsive Disorder (OCD) | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: SE (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2018-004618-17 | Sponsor Protocol Number: RITS-PS-2019 | Start Date*: 2019-04-24 |
Sponsor Name:Region Örebro län | ||
Full Title: Rituximab - Immunotherapy for Schizophrenia spectrum disorder in adults. An open pilot study. | ||
Medical condition: Treatment-resistant patients with schizophrenia spectrum disorder (SSD) | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: SE (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2019-000413-36 | Sponsor Protocol Number: BGB-3111-306 | Start Date*: 2020-02-24 | |||||||||||
Sponsor Name:BeiGene, Ltd. | |||||||||||||
Full Title: A Phase 3 Randomized, Open-Label, Multicenter Study Comparing Zanubrutinib (BGB-3111) plus Rituximab Versus Bendamustine plus Rituximab in Patients with Previously Untreated Mantle Cell Lymphoma Wh... | |||||||||||||
Medical condition: Mantle Cell Lymphoma | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Trial now transitioned) GB (GB - no longer in EU/EEA) AT (Trial now transitioned) DE (Ongoing) ES (Ongoing) FR (Trial now transitioned) IE (Trial now transitioned) PT (Trial now transitioned) NL (Trial now transitioned) IT (Trial now transitioned) RO (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2007-000222-51 | Sponsor Protocol Number: 06_DOG05_44 | Start Date*: 2007-09-07 |
Sponsor Name:Southampton University Hospitals NHS Trust | ||
Full Title: Short CHemo RadioImmunotherapy in Follicular Trial of 90Y Ibritumomab tiuxetan (ZevalinTM) as therapy for first and second relapse in Follicular Lymphoma | ||
Medical condition: Follicular Lymphoma First and second relapse of Follicular Lymphoma grade 1, 2, 3a. | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (Prematurely Ended) | ||
Trial results: (No results available) |
EudraCT Number: 2006-004673-98 | Sponsor Protocol Number: ML 20538 | Start Date*: 2006-10-16 |
Sponsor Name:Roche (Hungary) Ltd. | ||
Full Title: Efficacy of Rituximab treatment in patients with rheumatoid arthritis having inadequate response to TNF blocker | ||
Medical condition: To investigate the efficacy of treatment with Rituximab (MabThera®) in patients with active RA whose current treatment with one or more TNF-blocker (Etanercept - Enbrel®, Infliximab – Remicade® or ... | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: HU (Completed) | ||
Trial results: View results |
EudraCT Number: 2005-004740-31 | Sponsor Protocol Number: | Start Date*: 2005-12-21 | |||||||||||
Sponsor Name:University of Copenhagen | |||||||||||||
Full Title: Efficacy of B-cell depletion with rituximab on oral, ocular and general disease manifestations in patients with primary Sjögren disease | |||||||||||||
Medical condition: Previously treated patients with primary Sjögrens disease | |||||||||||||
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Population Age: Adults | Gender: Female | ||||||||||||
Trial protocol: DK (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2011-004908-37 | Sponsor Protocol Number: IRIS | Start Date*: 2011-10-21 | |||||||||||
Sponsor Name:FONDAZIONE CENTRO S. RAFFAELE DEL MONTE TABOR | |||||||||||||
Full Title: Phase II study on activity and tolerability of intralesional rituximab in relapsed or refractory patients affected by indolentCD-20 positive lymphoma of conjuntiva; evaluation of activity of adding... | |||||||||||||
Medical condition: indolent CD-20 positive lymphoma of conjunctiva | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2017-002290-19 | Sponsor Protocol Number: CC-5013-NHL-008 | Start Date*: 2017-12-07 |
Sponsor Name:Celgene Corporation | ||
Full Title: A Phase 3b randomized study of lenalidomide (CC-5013) plus rituximab maintenance therapy followed by lenalidomide single-agent maintenance versus rituximab maintenance in subjects with relapsed/ref... | ||
Medical condition: relapsed/refractory follicular, marginal zone or mantle cell lymphoma | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: DE (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2010-023335-41 | Sponsor Protocol Number: 16011 | Start Date*: 2011-11-23 | |||||||||||
Sponsor Name:Abbott | |||||||||||||
Full Title: A Phase 1b/2 Study of TRU-016 in Combination with Rituximab and Bendamustine in Subjects with Relapsed Indolent Lymphoma | |||||||||||||
Medical condition: Relapsed Indolent Lymphoma | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: AT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2007-001666-32 | Sponsor Protocol Number: APM4083g | Start Date*: 2007-12-05 | |||||||||||
Sponsor Name:Genentech Inc | |||||||||||||
Full Title: A PHASE II, SINGLE-ARM, OPEN-LABEL STUDY OF THE SAFETY,PHARMACOKINETICS, AND EFFICACY OF MULTIPLE DOSES OF APOMAB ADMINISTERED INTRAVENOUSLY IN COMBINATION WITH RITUXIMAB IN PATIENTS WITH FOLLICULA... | |||||||||||||
Medical condition: Follicular, CD20-Positive B-Cell Non-Hodgkin's Lymphoma | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Prematurely Ended) BE (Completed) GB (Prematurely Ended) ES (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2020-002765-34 | Sponsor Protocol Number: MabionCD20-003RA | Start Date*: 2021-10-21 | |||||||||||
Sponsor Name:Mabion S.A. | |||||||||||||
Full Title: A Double-Blind, Randomized, Parallel-Group Study to Investigate the Pharmacokinetic and Clinical Similarity Between MabionCD20 (manufactured in commercial scale), EU-approved MabThera® and US-licen... | |||||||||||||
Medical condition: Moderate-to-severe rheumatoid arthritis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2007-005580-95 | Sponsor Protocol Number: FL2008 RGM | Start Date*: 2008-09-19 | |||||||||||
Sponsor Name:Goelams | |||||||||||||
Full Title: An open label, multicenter, non randomized phase II study to evaluate anti-tumor efficacy and safety of GM-CSF (sargramostim, Leukine®) associated with Rituximab (MabThera®) in patients with follic... | |||||||||||||
Medical condition: This study evaluate anti-tumor efficacy and safety of GM-CSF (sargramostim, Leukine®) associated with Rituximab (MabThera®) in patients with non bulky follicular non Hodgkin’s lymphoma with no prio... | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2011-002896-40 | Sponsor Protocol Number: B3281001 | Start Date*: 2012-08-14 | |||||||||||
Sponsor Name:Pfizer Inc., 235 East 42nd Street, New York, NY 10017 | |||||||||||||
Full Title: A RANDOMIZED, DOUBLE-BLIND, STUDY COMPARING THE PHARMACOKINETICS AND PHARMACODYNAMICS, AND ASSESSING THE SAFETY OF PF-05280586 AND RITUXIMAB IN SUBJECTS WITH ACTIVE RHEUMATOID ARTHRITIS ON A BACKGR... | |||||||||||||
Medical condition: RHEUMATOID ARTHRITIS | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) ES (Completed) DE (Completed) PL (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2012-002062-13 | Sponsor Protocol Number: WA25615 | Start Date*: 2013-01-18 | ||||||||||||||||
Sponsor Name:F. Hoffmann-La Roche Ltd. | ||||||||||||||||||
Full Title: A Phase IIa, International, Multicenter, Open-Label, Uncontrolled Study to Evaluate the Safety and Pharmacokinetics of 4× 375 mg/m2 Intravenous Rituximab in Pediatric Patients with Severe Granul... | ||||||||||||||||||
Medical condition: granulomatosis with polyangiitis (Wegener’s) and microscopic polyangiitis | ||||||||||||||||||
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Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | |||||||||||||||||
Trial protocol: GB (Completed) DE (Completed) IT (Completed) | ||||||||||||||||||
Trial results: View results |
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