- Trials with a EudraCT protocol (414)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
414 result(s) found for: Acute Lymphoblastic Leukemia (ALL).
Displaying page 9 of 21.
EudraCT Number: 2011-003430-13 | Sponsor Protocol Number: AALL0932 | Start Date*: 2014-01-14 | ||||||||||||||||
Sponsor Name:Children's Oncology Group | ||||||||||||||||||
Full Title: Treatment of Patients with Newly Diagnosed Standard Risk B-Lymphoblastic Leukemia (B-ALL) or Localized B-lineage Lymphoblastic Lymphoma (B-LLy) | ||||||||||||||||||
Medical condition: Acute Lymphoblastic Leukemia and Lymphoblastic Lymphoma | ||||||||||||||||||
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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: 2014-001700-21 | Sponsor Protocol Number: 20130320 | Start Date*: 2015-02-19 | |||||||||||||||||||||
Sponsor Name:Amgen Inc. | |||||||||||||||||||||||
Full Title: An Open-Label, Multi-center, Expanded Access Protocol of Blinatumomab for the Treatment of Pediatric and Adolescent Subjects with Relapsed and/or Refractory B-precursor Acute Lymphoblastic Leukemia... | |||||||||||||||||||||||
Medical condition: Pediatric and Adolescent Subjects with Relapsed and/or Refractory B-precursor Acute Lymphoblastic Leukemia (ALL) | |||||||||||||||||||||||
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Population Age: Infants and toddlers, Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: GB (Completed) DE (Completed) IT (Completed) AT (Completed) FR (Completed) | |||||||||||||||||||||||
Trial results: View results |
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: 2019-003117-33 | Sponsor Protocol Number: Pevonedistat-2002 | Start Date*: Information not available in EudraCT | |||||||||||||||||||||
Sponsor Name:Millennium Pharmaceuticals, Inc. | |||||||||||||||||||||||
Full Title: A Randomized, Open-label, Controlled, Phase 2 Study of Pevonedistat, Venetoclax, and Azacitidine Versus Venetoclax Plus Azacitidine in Adults With Newly Diagnosed Acute Myeloid Leukemia Who Are Unf... | |||||||||||||||||||||||
Medical condition: Acute Myeloid Leukemia (AML) | |||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: PL (Trial now transitioned) IT (Trial now transitioned) FR (Completed) | |||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2005-004599-19 | Sponsor Protocol Number: INTERFANT-06 | Start Date*: 2005-11-24 | |||||||||||
Sponsor Name:A.I.E.O.P. - ASSOCIAZIONE ITALIANA EMATOLOGIA ONCOLOGIA PEDIATRICA | |||||||||||||
Full Title: INTERNATIONAL COLLABORATIVE TREATMENT PROTOCOL FOR INFANTS UNDER ONE YEAR WITH ACUTE LYMPHOBLASTIC OR BIPHENOTYPIC LEUKEMIA | |||||||||||||
Medical condition: acute lymphoblastic leukemia (ALL) or biphenotypic leukemia | |||||||||||||
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Population Age: Newborns, Infants and toddlers, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) BE (Completed) FR (Ongoing) DE (Completed) GB (Completed) AT (Completed) PT (Completed) DK (Completed) IE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2020-005019-29 | Sponsor Protocol Number: Rux-cALL-Pol_2020 | Start Date*: Information not available in EudraCT | ||||||||||||||||
Sponsor Name:Medical University of Lodz | ||||||||||||||||||
Full Title: Single-arm interventional study with ruxolitinib and AIOEP-BFM2017 chemotherapy in children with acute lymphoblastic leukemia and confirmed activation of JAK/STAT pathway. | ||||||||||||||||||
Medical condition: Acute Lymphoblastic Leukemia with confirmed activating of JAK/STAT pathway in children and adolescents <18 years of age | ||||||||||||||||||
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Population Age: Infants and toddlers, Children, Adolescents, Under 18 | Gender: Male, Female | |||||||||||||||||
Trial protocol: PL (Trial now transitioned) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2007-004270-43 | Sponsor Protocol Number: AIEOP-BFMALL2009 | Start Date*: Information not available in EudraCT | |||||||||||
Sponsor Name:Universitätsklinikum Schleswig-Holstein, Campus Kiel | |||||||||||||
Full Title: International collaborative treatment protocol for children and adolescents with acute lymphoblastic leukemia | |||||||||||||
Medical condition: acute lymphoblastic leukemia in children and adolescents 1 to <18 years of age | |||||||||||||
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Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) CZ (Completed) AT (Completed) IT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2015-004202-41 | Sponsor Protocol Number: PONALFIL | Start Date*: 2016-03-21 | |||||||||||
Sponsor Name:Fundación PETHEMA | |||||||||||||
Full Title: CONCURRENT PONATINIB WITH CHEMOTHERAPY FOR YOUNG ADULTS WITH NEWLY DIAGNOSED PHILADELPHIA CHROMOSOME-POSITIVE ACUTE LYMPHOBLASTIC LEUKEMIA. | |||||||||||||
Medical condition: NEWLY DIAGNOSED PHILADELPHIA CHROMOSOME-POSITIVE ACUTE LYMPHOBLASTIC LEUKEMIA. | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2004-001853-27 | Sponsor Protocol Number: BIOV-111 | Start Date*: 2005-10-19 | |||||||||||
Sponsor Name:Bioenvision Limited | |||||||||||||
Full Title: A Phase II, Open-Label Study of Clofarabine in Paediatric Patients with Refractory / Relapsed Acute Lymphoblastic Leukaemia | |||||||||||||
Medical condition: Relapsed or refractory acute lymphoblastic leukaemia (ALL) in children | |||||||||||||
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Population Age: Newborns, Infants and toddlers, Children, Adolescents, Under 18, Adults | Gender: Male, Female | ||||||||||||
Trial protocol: AT (Completed) IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2015-004293-15 | Sponsor Protocol Number: UCART19_02(CL1-68587-001) | Start Date*: 2016-05-24 | |||||||||||
Sponsor Name:Institut de Recherches Internationales Servier (I.R.I.S) | |||||||||||||
Full Title: A phase 1, open label, non-comparative, study to evaluate the safety and the ability of UCART19 to induce molecular remission in paediatric patients with relapsed /refractory B-cell acute lymphobla... | |||||||||||||
Medical condition: Paediatric relapsed or refractory CD19-positive B-cell acute lymphoblastic leukemia | |||||||||||||
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Population Age: Infants and toddlers, Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) BE (Completed) FR (Completed) ES (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2008-002219-42 | Sponsor Protocol Number: BCX1777-108 | Start Date*: 2009-01-26 | ||||||||||||||||
Sponsor Name:Mundipharma Research Limited | ||||||||||||||||||
Full Title: A Phase I/II Pharmacokinetic Study of Intravenous and Oral Forodesine in Children with Relapsed or Refractory T-cell or B-cell Precursor Acute Lymphoblastic Leukaemia or T-cell Non- Hodgkin’s Lymphoma | ||||||||||||||||||
Medical condition: T-cell or B-cell precursor (BCP) acute lymphoblastic leukaemia (T-ALL or BCP-ALL) or T-cell Non Hodgkin’s lymphoma (T-NHL) | ||||||||||||||||||
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Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | |||||||||||||||||
Trial protocol: DE (Completed) FR (Completed) AT (Prematurely Ended) GB (Prematurely Ended) NL (Prematurely Ended) IT (Prematurely Ended) CZ (Prematurely Ended) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2021-000761-33 | Sponsor Protocol Number: KB-ENTO-3001 | Start Date*: 2022-01-03 | |||||||||||
Sponsor Name:Kronos Bio, Inc. | |||||||||||||
Full Title: A Phase 3, Randomized, Double-blind, Placebo-controlled Study to Assess the Efficacy and Safety of Entospletinib in Combination With Intensive Induction and Consolidation Chemotherapy in Adults Wit... | |||||||||||||
Medical condition: Acute Myeloid Leukemia | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Prematurely Ended) ES (Prematurely Ended) HU (Prematurely Ended) CZ (Prematurely Ended) IT (Prematurely Ended) FR (Prematurely Ended) PL (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2015-005009-35 | Sponsor Protocol Number: KTE-C19-103 | Start Date*: 2018-09-25 | |||||||||||
Sponsor Name:Kite Pharma Inc. | |||||||||||||
Full Title: A Phase 1/2 Multi-Center Study Evaluating the Safety and Efficacy of KTE-X19 in Adult Subjects with Relapsed/Refractory B-precursor Acute Lymphoblastic Leukemia (r/r ALL) (ZUMA-3) | |||||||||||||
Medical condition: Relapsed/Refractory B-precursor Acute Lymphoblastic Leukemia (r/r ALL) | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) NL (Completed) FR (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2016-003904-29 | Sponsor Protocol Number: RG_16-186 | Start Date*: 2017-07-12 | |||||||||||
Sponsor Name:University of Birmingham | |||||||||||||
Full Title: International phase I/II expansion trial of the MEK inhibitor selumetinib in combination with dexamethasone for the treatment of relapsed/refractory RAS-pathway mutated paediatric and adult Acute L... | |||||||||||||
Medical condition: Relapsed/refractory acute lymphoblatic leukaemia with mutation in the RAS pathway | |||||||||||||
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Population Age: Infants and toddlers, Children, Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) NL (Completed) FR (Prematurely Ended) DK (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2016-004724-34 | Sponsor Protocol Number: PRAN-16-52 | Start Date*: 2017-08-11 | |||||||||||
Sponsor Name:Helsinn Healthcare SA | |||||||||||||
Full Title: A Phase III, Double-Blind, Placebo-Controlled, Multicenter, Randomized Study Of Pracinostat In Combination With Azacitidine In Patients ≥18 Years With Newly Diagnosed Acute Myeloid Leukemia Unfit F... | |||||||||||||
Medical condition: Newly diagnosed Acute Myeloid Leukemia patients | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Prematurely Ended) GB (Prematurely Ended) CZ (Prematurely Ended) AT (Prematurely Ended) HU (Completed) ES (Prematurely Ended) FR (Prematurely Ended) IT (Prematurely Ended) RO (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2020-004768-24 | Sponsor Protocol Number: UCART22_01 | Start Date*: 2021-12-06 | |||||||||||
Sponsor Name:CELLECTIS SA | |||||||||||||
Full Title: Open label dose-escalation and dose-expansion study to evaluate the safety, expansion, persistence and clinical activity of UCART22 (allogeneic engineered T-cells expressing anti-CD22 Chimeric Anti... | |||||||||||||
Medical condition: Acute Lymphoblastic Leukaemia. | |||||||||||||
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Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2009-013093-41 | Sponsor Protocol Number: AC220-002 | Start Date*: 2010-02-05 | |||||||||||
Sponsor Name:Ambit Biosciences Corporation | |||||||||||||
Full Title: A PHASE 2 OPEN-LABEL, AC220 MONOTHERAPY EFFICACY (ACE) STUDY IN PATIENTS WITH ACUTE MYELOID LEUKEMIA (AML) WITH FLT3-ITD ACTIVATING MUTATIONS | |||||||||||||
Medical condition: Acute Myeloid Leukemia | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Completed) DE (Completed) ES (Completed) NL (Completed) PL (Completed) IT (Completed) GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2005-005106-23 | Sponsor Protocol Number: ALLSCT06BFMi | Start Date*: 2007-06-27 | |||||||||||
Sponsor Name:St. Anna Kinderkrebsforschung | |||||||||||||
Full Title: Allogenic stem cell transplantation in children and adolescents with acute lymphoblastic leukaemia | |||||||||||||
Medical condition: very high risk acute lymphoblastic leukaemia in children and adolescents with indicaton for allogenic hematopoetic stem cell transplantation | |||||||||||||
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Population Age: Infants and toddlers, Children, Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: AT (Completed) IT (Ongoing) | |||||||||||||
Trial results: View results |
EudraCT Number: 2010-022855-46 | Sponsor Protocol Number: EWALL-PH-02 | Start Date*: 2011-07-13 |
Sponsor Name:Dekan des Fachbereichs Medizin der Goethe Universität, represented by the Coordinating Investigator | ||
Full Title: AN OPEN LABEL PHASE II STUDY TO EVALUATE THE EFFICACY AND SAFETY OF INDUCTION AND CONSOLIDATION THERAPY WITH NILOTINIB IN COMBINATION WITH CHEMOTHERAPY IN PATIENTS AGED 55 YEARS AND OVER WITH PHIL... | ||
Medical condition: Philadelphia chromosome positive Acute Lymphoblastic Leukemia in elderly Patients (55 years and older) | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: DE (Completed) IT (Prematurely Ended) ES (Completed) | ||
Trial results: View results |
EudraCT Number: 2018-003350-25 | Sponsor Protocol Number: SPON1751-19 | Start Date*: 2019-09-05 | |||||||||||
Sponsor Name:Cardiff University | |||||||||||||
Full Title: An open label, 3-arm, Randomised phase II study to Compare the Safety and Efficacy of Ponatinib in combination with either Chemotherapy or Blinatumomab with Imatinib plus Chemotherapy as front-line... | |||||||||||||
Medical condition: Philadelphia chromosome positive (Ph+ or BCR-ABL+) Acute Lymphoblastic Leukaemia (ALL) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) FR (Trial now transitioned) SE (Trial now transitioned) FI (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
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