- Trials with a EudraCT protocol (62)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
62 result(s) found for: Precursor B-cell lymphoblastic leukemia.
Displaying page 1 of 4.
EudraCT Number: 2008-002286-32 | Sponsor Protocol Number: 6125 | Start Date*: 2009-08-10 | ||||||||||||||||
Sponsor Name:Queen Mary Medical University of London | ||||||||||||||||||
Full Title: Phase I/II Study combining humanised anti-CD20 (veltuzumab), anti-CD22 (epratuzumab) and both monoclonal antibodies with chemotherapy in adults with recurrent B precursor acute lymphoblastic leukae... | ||||||||||||||||||
Medical condition: This is a phase I/ II trial to determine the efficacy of intravenous veltuzumab and epratuzmab either individually or together in combination with chemotherapy in patients with recurrent acute lymp... | ||||||||||||||||||
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Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: GB (Prematurely Ended) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2021-001535-99 | Sponsor Protocol Number: CCTL019BUS03 | Start Date*: 2022-03-14 | |||||||||||
Sponsor Name:Novartis Pharmaceuticals Corporation | |||||||||||||
Full Title: A phase II, open label, multi-center trial to determine the efficacy and safety of tisagenlecleucel re-infusion in Pediatric and Adolescent Young Adult (AYA) patients with acute lymphoblastic leuke... | |||||||||||||
Medical condition: Paediatric patients with B-cell acute lymphoblastic leukaemia | |||||||||||||
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Population Age: Infants and toddlers, Children, Adolescents, Under 18, Adults | Gender: Male, Female | ||||||||||||
Trial protocol: Outside EU/EEA | |||||||||||||
Trial results: View results |
EudraCT Number: 2015-001697-17 | Sponsor Protocol Number: R1979-ONC-1504 | Start Date*: 2015-12-01 | ||||||||||||||||||||||||||||||||||||||||||||||
Sponsor Name:Regeneron Pharmaceuticals, Inc | ||||||||||||||||||||||||||||||||||||||||||||||||
Full Title: A Phase 1 Study to Assess Safety and Tolerability of REGN1979, an anti-CD20 x anti- CD3 bispecific monoclonal antibody, and REGN2810, an anti-programmed death-1 monoclonal antibody, in Patients wit... | ||||||||||||||||||||||||||||||||||||||||||||||||
Medical condition: B-cell malignancies | ||||||||||||||||||||||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||||||||||||||||||||||
Trial protocol: DE (Completed) ES (Restarted) | ||||||||||||||||||||||||||||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2016-000296-24 | Sponsor Protocol Number: CL1-68587-002 | Start Date*: 2017-10-20 | |||||||||||
Sponsor Name:Institut de Recherches Internationales Servier (I.R.I.S) | |||||||||||||
Full Title: Phase I, open label, dose-escalation study to evaluate the safety, expansion and persistence of a single dose of UCART19 (allogeneic engineered T-cells expressing anti-CD19 chimeric antigen recepto... | |||||||||||||
Medical condition: Patients with relapsed or refractory CD19 positive B-cell acute lymphoblastic leukaemia (B-ALL). | |||||||||||||
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Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2017-000766-30 | Sponsor Protocol Number: HO146 | Start Date*: 2018-03-09 | |||||||||||
Sponsor Name:HOVON Foundation | |||||||||||||
Full Title: Blinatumomab added to prephase and consolidation therapy in precursor B-acute lymphoblastic leukemia in adults. A phase II trial. | |||||||||||||
Medical condition: Precursor B-acute lymphoblastic leukemia | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Trial now transitioned) BE (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2016-002972-29 | Sponsor Protocol Number: CART19-BE-01 | Start Date*: 2017-05-16 | ||||||||||||||||||||||||||
Sponsor Name:IDIBAPS | ||||||||||||||||||||||||||||
Full Title: Pilot study on the infusion of differentiated autologous T-cells from peripheral blood, expanded and transduced with a lentivirus to express a chimeric antigen receptor with anti-CD19 specificity (... | ||||||||||||||||||||||||||||
Medical condition: Patients with leukemia or lymphoma refractory to therapy | ||||||||||||||||||||||||||||
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Population Age: Children, Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||
Trial protocol: ES (Ongoing) | ||||||||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2022-002190-28 | Sponsor Protocol Number: SHP674-201\CL1-95014-001 | Start Date*: 2022-07-04 | |||||||||||
Sponsor Name:Institut de Recherches Internationales Servier (IRIS) | |||||||||||||
Full Title: A Phase 2 Clinical Study of SHP674 in Patients with Newly Diagnosed, Untreated Acute Lymphoblastic Leukemia | |||||||||||||
Medical condition: Acute Lymphoblastic Leukemia | |||||||||||||
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Population Age: Infants and toddlers, Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: Outside EU/EEA | |||||||||||||
Trial results: View results |
EudraCT Number: 2012-003101-10 | Sponsor Protocol Number: CD-ON-CAT-8015-1036 | Start Date*: 2013-05-03 | ||||||||||||||||
Sponsor Name:MedImmune, LLC | ||||||||||||||||||
Full Title: A Phase 2, Multicenter, Single-arm Study of Moxetumomab Pasudotox in Pediatric Subjects with Relapsed or Refractory Pediatric Acute Lymphoblastic Leukemia (pALL) or Lymphoblastic Lymphoma of B-cel... | ||||||||||||||||||
Medical condition: Rediatric Subjects with Relapsed or Refractory Pediatric Acute Lymphoblastic Leukemia (pALL) or Lymphoblastic Lymphoma of B-cell Origin | ||||||||||||||||||
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Population Age: Infants and toddlers, Children, Adolescents, Under 18 | Gender: Male, Female | |||||||||||||||||
Trial protocol: GB (Completed) DE (Completed) FR (Completed) IT (Completed) ES (Completed) NL (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2014-001673-14 | Sponsor Protocol Number: CCTL019A2205B | Start Date*: 2015-10-06 | ||||||||||||||||
Sponsor Name:Novartis Pharma Services AG | ||||||||||||||||||
Full Title: Long Term Follow-Up of Patients Exposed to Lentiviral-Based CAR T-Cell Therapy | ||||||||||||||||||
Medical condition: All patients who have been treated with chimeric antigen receptor (CAR) T-cell therapy in the context of a prior Novartis sponsored or supported study for any indication. | ||||||||||||||||||
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Population Age: Children, Under 18, Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: AT (Trial now transitioned) DE (Trial now transitioned) ES (Ongoing) NO (Trial now transitioned) BE (Trial now transitioned) NL (Trial now transitioned) FR (Trial now transitioned) DK (Trial now transitioned) GB (GB - no longer in EU/EEA) SE (Trial now transitioned) FI (Trial now transitioned) IT (Trial now transitioned) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2016-004942-27 | Sponsor Protocol Number: P16/11 | Start Date*: 2017-07-17 | |||||||||||
Sponsor Name:Centre Hospitalier de Versailles | |||||||||||||
Full Title: A Phase 2 Study of Inotuzumab Ozogamicin (INO) Combined to Chemotherapy in Older Patients with Philadelphia Chromosome-negative CD22+ B-cell Precursor Acute Lymphoblastic Leukemia | |||||||||||||
Medical condition: Philadelphia chromosome (Ph)-negative CD22+ B-cell Precursor (BCP) Acute Lymphoblastic Leukemia (ALL) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Completed) FI (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2018-004336-30 | Sponsor Protocol Number: CYTB323A12101 | Start Date*: 2020-04-07 |
Sponsor Name:Novartis Pharma AG | ||
Full Title: Phase I/II, open label, multicenter study of rapcabtagene autoleucel in adult patients with CLL/SLL, 3L+ DLBCL, r/r ALL and 1L HR LBCL. | ||
Medical condition: ALL, CLL/SLL and DLBCL and High-Risk LBCL. | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: AT (Trial now transitioned) DE (Trial now transitioned) | ||
Trial results: (No results available) |
EudraCT Number: 2017-004714-25 | Sponsor Protocol Number: REALIB-LLA-2017 | Start Date*: 2018-07-25 | |||||||||||
Sponsor Name:Fundación PETHEMA | |||||||||||||
Full Title: Phase I-II trial, open and nonrandomized, to assess the role of Idelalisib in patients with acute lymphoblastic leukemia (ALL) relapsed or refractory to other treatments, and in elderly patients wi... | |||||||||||||
Medical condition: Acute lymphoblastic leukemia | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2012-002961-36 | Sponsor Protocol Number: EFC11603 | Start Date*: 2013-02-11 | |||||||||||
Sponsor Name:Sanofi-aventis recherche et développement | |||||||||||||
Full Title: Phase II two stage dose finding run-in study of SAR3419, an anti-CD19 antibody-maytansine conjugate,administered as a single agent by intravenous infusion in patients with relapsed or Refractory Ac... | |||||||||||||
Medical condition: Acute lymphoblastic leukemia | |||||||||||||
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Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2020-004894-29 | Sponsor Protocol Number: CL2-95014-002 | Start Date*: 2021-09-17 | |||||||||||
Sponsor Name:Institut de Recherches Internationales Servier | |||||||||||||
Full Title: A multicentre, Phase II Randomized study, Open-label, with 2-arm Parallel Group, comparing the pharmacokinetics of the Liquid and the Lyophilized Formulations of pegaspargase (S95014) in Treatment ... | |||||||||||||
Medical condition: Newly diagnosed paediatric patients with Acute Lymphoblastic Leukemia | |||||||||||||
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Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: Outside EU/EEA | |||||||||||||
Trial results: View results |
EudraCT Number: 2021-004287-98 | Sponsor Protocol Number: TCD17197 | Start Date*: 2022-03-16 | |||||||||||||||||||||
Sponsor Name:Sanofi-Aventis Recherche & Developpement | |||||||||||||||||||||||
Full Title: An open-label, first-in-human, dose-escalation/expansion study of SAR443579 administered as single agent by intravenous infusion in patients with relapsed or refractory acute myeloid leukemia (R/R ... | |||||||||||||||||||||||
Medical condition: Relapsed or refractory acute myeloid leukemia (R/R AML), B-cell acute lymphoblastic leukemia (B-ALL) or high risk-myelodysplasia (HR-MDS) | |||||||||||||||||||||||
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Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: NL (Trial now transitioned) | |||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2017-003377-34 | Sponsor Protocol Number: 54767414ALL2005 | Start Date*: 2018-07-31 | |||||||||||||||||||||
Sponsor Name:Janssen-Cilag International N.V. | |||||||||||||||||||||||
Full Title: An Open-label, Multicenter, Phase 2 Study Evaluating the Efficacy and Safety of Daratumumab in Pediatric and Young Adult Subjects ≥1 and ≤30 Years of Age With Relapsed/Refractory Precursor B-cell o... | |||||||||||||||||||||||
Medical condition: Relapsed/Refractory Precursor B-cell or T-cell Acute Lymphoblastic Leukemia or Lymphoblastic Lymphoma | |||||||||||||||||||||||
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Population Age: Infants and toddlers, Children, Adolescents, Under 18, Adults | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) DE (Completed) BE (Completed) FR (Completed) ES (Completed) SE (Completed) NL (Completed) IT (Completed) Outside EU/EEA | |||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2019-001937-16 | Sponsor Protocol Number: AUTO1-AL1 | Start Date*: 2020-02-17 | |||||||||||
Sponsor Name:Autolus Limited | |||||||||||||
Full Title: An Open-Label, Multi-Centre, Phase Ib/II Study Evaluating The Safety and Efficacy Of AUTO1, A CAR T Cell Treatment Targeting CD19, In Adult Patients With Relapsed Or Refractory B Cell Acute Lymphob... | |||||||||||||
Medical condition: Relapsed or refractory B cell acute lymphoblastic 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) |
EudraCT Number: 2008-005798-36 | Sponsor Protocol Number: HOVON100ALL/EORTC06083 | Start Date*: 2009-08-31 | ||||||||||||||||
Sponsor Name:HOVON Foundation | ||||||||||||||||||
Full Title: Clofarabine added to prephase and consolidation therapy in acute lymphoblastic leukemia in adults. | ||||||||||||||||||
Medical condition: Primary previously untreated B or T-lineage ALL (excluding ALL with mature B-cell phenotype, but including Philadelphia positive or BCR-ABL positive ALL) or previously untreated T-LBL | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: NL (Completed) BE (Prematurely Ended) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2022-001101-52 | Sponsor Protocol Number: CART19-BE-03Ped | Start Date*: 2022-11-07 | |||||||||||
Sponsor Name:Fundació Privada per a la Recerca i la Docència Sant Joan de Déu | |||||||||||||
Full Title: Phase 2 study of the infusion of autologous, differentiated, peripheral blood T-cells expanded and transduced with a lentivirus to express a chimeric antigen receptor with anti-CD19 specificity (A3... | |||||||||||||
Medical condition: CD19+ acute lymphoid leukemia resistant or refractory to treatment | |||||||||||||
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Population Age: Newborns, Infants and toddlers, Children, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2009-012717-22 | Sponsor Protocol Number: UCL/08/0167 | Start Date*: 2010-01-13 | |||||||||||
Sponsor Name:University College London | |||||||||||||
Full Title: UKALL14 - A randomized trial for adults with newly diagnosed acute lymphoblastic leukemia | |||||||||||||
Medical condition: Acute Lymphoblastic Leukemia (ALL) | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) | |||||||||||||
Trial results: (No results available) |
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