- Trials with a EudraCT protocol (380)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (2)
380 result(s) found for: Lymphoid leukemia.
Displaying page 6 of 19.
EudraCT Number: 2015-005281-29 | Sponsor Protocol Number: IVAC-ALL-1 | Start Date*: 2016-06-07 | ||||||||||||||||
Sponsor Name:University Hospital Tuebingen | ||||||||||||||||||
Full Title: Prospective phase I/II study: Patient-individualized peptide vaccination based on whole exome sequencing with adjuvant GM-CSF in children with relapsed acute lymphoblastic leukemia | ||||||||||||||||||
Medical condition: Relapsed acute lymphatic leukemia | ||||||||||||||||||
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Population Age: Children, Under 18 | Gender: Male, Female | |||||||||||||||||
Trial protocol: DE (Completed) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2010-024264-18 | Sponsor Protocol Number: MT103-205 | Start Date*: 2011-11-23 | |||||||||||
Sponsor Name:Amgen Research (Munich) GmbH | |||||||||||||
Full Title: A Single-Arm Multicenter Phase II Study preceded by Dose Evaluation to Investigate the Efficacy, Safety, and Tolerability of the BiTE® Antibody Blinatumomab (MT103) in Pediatric and Adolescent Pati... | |||||||||||||
Medical condition: Pediatric and adolescent patients with B-precursor ALL in second or later bone marrow relapse, in any marrow relapse after allogeneic HSCT, or refractory to other treatments. | |||||||||||||
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Population Age: Infants and toddlers, Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) AT (Completed) NL (Completed) IT (Completed) GB (Completed) Outside EU/EEA | |||||||||||||
Trial results: View results |
EudraCT Number: 2012-001947-31 | Sponsor Protocol Number: TUD-CLL-X4-054 | Start Date*: 2013-02-27 | |||||||||||
Sponsor Name:Technische Universität Dresen | |||||||||||||
Full Title: Ofatumumab Induction and Maintenance in Elderly Patients with Poor Risk CLL in the Context of Allogeneic Transplantation: CLLX4 Trial | |||||||||||||
Medical condition: Patients aged >55 years with a diagnosis of CLL according to WHO criteria confirmed by flow cytometry of peripheral blood or bone marrow and a poor-risk disease according to the EBMT CLL Transplan... | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2012-000634-20 | Sponsor Protocol Number: LENOFA01 | Start Date*: 2012-11-05 | |||||||||||
Sponsor Name:A.O. UNIVERSITARIA INTEGRATA DI VERONA | |||||||||||||
Full Title: Multicenter, pilot study to assess the safety and efficacy of Lenalidomide and Ofatumumab combination (Lenofa) in chronic lymphocytic leukenia (CLL) patients relapsed or refractory after fludarab... | |||||||||||||
Medical condition: Chronic Lymphocytic Leukemia patients relapsed or refractory after fludarabine containing regimens | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2008-002204-25 | Sponsor Protocol Number: 152CL202 | Start Date*: 2009-04-21 | |||||||||||
Sponsor Name:Biogen Idec Ltd | |||||||||||||
Full Title: A Phase 2, Randomized, Open-Label Study to Evaluate the Safety and Efficacy of Fludarabine, Cyclophosphamide, and Rituximab (FCR) in Combination with Lumiliximab Versus FCR Alone in Subjects with P... | |||||||||||||
Medical condition: Previously Untreated Chronic Lymphocytic Leukemia (CLL) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Prematurely Ended) FR (Completed) BE (Completed) AT (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2015-004985-27 | Sponsor Protocol Number: HO139 | Start Date*: 2016-09-29 | |||||||||||
Sponsor Name:HOVON Foundation | |||||||||||||
Full Title: A prospective, open-label, multicenter randomized phase-II trial to evaluate the efficacy and safety of a sequential regimen of obinutuzumab (Gazyvaro) followed by obinutuzumab and venetoclax, foll... | |||||||||||||
Medical condition: Chronic Lymphocytic Leukemia | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2011-001955-35 | Sponsor Protocol Number: RG_11-054 | Start Date*: 2012-02-15 | |||||||||||||||||||||
Sponsor Name:University of Birmingham | |||||||||||||||||||||||
Full Title: Single Arm Phase II trial assessing the safety, compliance with and activity of Bezafibrate and medroxyProgesterone acetate (BaP) as non-toxic therapy against myeloid and lymphoid cancers | |||||||||||||||||||||||
Medical condition: Acute Myeloid Leukaemia (AML), Chronic Lymphocytic Leukaemia (CLL) and B-cell Non-Hodgkins Lymphoma (BNHL) | |||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: GB (Prematurely Ended) | |||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2010-018314-75 | Sponsor Protocol Number: MT103-203 | Start Date*: 2010-08-05 | |||||||||||
Sponsor Name:Amgen Research (Munich) GmbH | |||||||||||||
Full Title: A confirmatory multicenter, single-arm study to assess the efficacy, safety, and tolerability of the BiTE® antibody blinatumomab in adult patients with minimal residual disease (MRD) of B-precursor... | |||||||||||||
Medical condition: minimal residual disease (MRD) of B-precursor ALL | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) BE (Completed) GB (Completed) AT (Completed) ES (Completed) CZ (Completed) FR (Completed) PL (Completed) IT (Completed) NL (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2010-019119-39 | Sponsor Protocol Number: GIMEMALAL1509 | Start Date*: 2011-05-16 | |||||||||||
Sponsor Name:G.I.M.E.M.A. GRUPPO ITALIANO MALATTIE EMATOLOGICHE DELL'ADULTO | |||||||||||||
Full Title: A multicenter Total Therapy Strategy for De Novo Adult Philadelphia Chromosome Positive (Ph+) Acute Lymphoblastic Leukemia (ALL) Patients | |||||||||||||
Medical condition: De Novo Philadelphia Chromosome Positive (Ph+) Acute Lymphoblastic Leukemia (ALL) | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2006-006978-20 | Sponsor Protocol Number: HBS407 | Start Date*: 2007-11-21 | |||||||||||
Sponsor Name:Talon Therapeutics , Inc. | |||||||||||||
Full Title: A Phase 2 Study to Evaluate the Safety and Efficacy of Weekly Doses of Marqibo® (vincristine sulfate liposomes injection) in Adult Patients with Philadelphia Chromosome-negative Acute Lymphoblastic... | |||||||||||||
Medical condition: Philadelphia Chromosome-negative Acute Lymphoblastic Leukemia | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) GB (Prematurely Ended) | |||||||||||||
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: 2012-004461-41 | Sponsor Protocol Number: CR-AIR-007 | Start Date*: 2013-06-27 | |||||||||||||||||||||||||||||||
Sponsor Name:Kiadis Pharma Netherlands B.V. | |||||||||||||||||||||||||||||||||
Full Title: An exploratory, open-label, multicenter study to evaluate the safety and efficacy of ATIR, donor T-lymphocytes depleted ex vivo of host alloreactive T-cells, in patients with a hematologic malignan... | |||||||||||||||||||||||||||||||||
Medical condition: Patients with a hematologic malignancy (AML, ALL, or MDS) who are eligible for a haploidentical HSCT | |||||||||||||||||||||||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||||||||||||||||||||||
Trial protocol: BE (Completed) DE (Completed) GB (Completed) | |||||||||||||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2008-001612-20 | Sponsor Protocol Number: ML21445 | Start Date*: 2008-05-29 | |||||||||||
Sponsor Name:ROCHE | |||||||||||||
Full Title: A study of chlorambucil plus MabThera as induction therapy followed in responders by maintenance therapy versus observation on response rate in patients ≥ 60 years with previously untreated ... | |||||||||||||
Medical condition: CD20+ CLL, Binet stage C or Binet stages A-B | |||||||||||||
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Population Age: Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2005-003018-14 | Sponsor Protocol Number: CLL7 | Start Date*: 2006-03-02 |
Sponsor Name:AKH Vienna | ||
Full Title: Randomized phase III trial comparing early treatment with fludarabine, cyclophosphamide + rituximab versus deferred treatment in untreated Binet stage A patients with high risk of progression CLL 7... | ||
Medical condition: chronic lymphocytic leukaemia (CLL) | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: AT (Completed) CZ (Prematurely Ended) | ||
Trial results: View results |
EudraCT Number: 2020-002142-17 | Sponsor Protocol Number: CLL-Frail | Start Date*: 2021-11-24 | |||||||||||
Sponsor Name:University of Cologne | |||||||||||||
Full Title: CLL-Frail – A prospective, multicenter phase II trial of acalabrutinib in very old (≥80y) or frail CLL-Patients | |||||||||||||
Medical condition: Patients with CLL requiring treatment | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: AT (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2007-007587-21 | Sponsor Protocol Number: CLL10 | Start Date*: 2008-09-05 | |||||||||||
Sponsor Name:University of Cologne | |||||||||||||
Full Title: Phase III trial of combined immunochemotherapy with Fludarabine, Cyclophosphamide and Rituximab (FCR) versus Bendamustine and Rituximab (BR) in patients with previously untreated chronic lymphocyti... | |||||||||||||
Medical condition: patients (age 18 years or older) with chronic lymphocytic leukemia: Stage Binet C or stage Binet B and A requiring treatment | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) AT (Completed) DK (Completed) CZ (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2010-019554-41 | Sponsor Protocol Number: 16201 | Start Date*: 2010-10-19 | |||||||||||
Sponsor Name:Trubion Pharmaceuticals | |||||||||||||
Full Title: A Phase 1b/2 Open Label Study to Evaluate the Safety and Efficacy of TRU-016 in Combination with Bendamustine vs. Bendamustine Alone in Patients with Relapsed Chronic Lymphocytic Leukemia / Estudio... | |||||||||||||
Medical condition: leucemia linfocítica crónica | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Completed) AT (Completed) DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2019-001575-37 | Sponsor Protocol Number: 20180138 | Start Date*: 2020-03-04 | ||||||||||||||||
Sponsor Name:Amgen Inc. | ||||||||||||||||||
Full Title: Long-term Follow-up of Adult Philadelphia Chromosome-negative Acute Lymphoblastic Leukemia Relapsed Refractory Patients Enrolled in Study 00103311 | ||||||||||||||||||
Medical condition: Adult patients with relapsed and/or refractory B-precursor acute lymphoblastic leukaemialastic leukaemia | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: DE (Completed) IT (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2010-024520-15 | Sponsor Protocol Number: UCL/09/0387 | Start Date*: 2012-03-27 | |||||||||||
Sponsor Name:University College London | |||||||||||||
Full Title: A pilot study to establish the safety and efficacy of a combination of dexamethasone and lenalidomide in patients with relapsed or refractory chronic lymphocytic leukaemia (CLL) | |||||||||||||
Medical condition: Chronic lymphocytic leukaemia | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2009-010998-20 | Sponsor Protocol Number: HM09/8848 | Start Date*: 2009-06-25 | |||||||||||
Sponsor Name:Leeds Teaching Hospitals NHS Trust | |||||||||||||
Full Title: Attenuated dose Rituximab with ChemoTherapy In CLL: A randomised, phase IIB trial in previously untreated patients with Chronic Lymphocytic Leukaemia (CLL) to compare fludarabine, cyclophosphamide ... | |||||||||||||
Medical condition: Chronic Lymphocytic Leukaemia | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) | |||||||||||||
Trial results: (No results available) |
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