- Trials with a EudraCT protocol (306)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
306 result(s) found for: chronic lymphocytic leukemia.
Displaying page 10 of 16.
EudraCT Number: 2017-002848-32 | Sponsor Protocol Number: M-2017-322 | Start Date*: 2018-05-15 | |||||||||||||||||||||||||||||||
Sponsor Name:Miltenyi Biomedicine GmbH | |||||||||||||||||||||||||||||||||
Full Title: A phase I/II safety, dose finding and feasibility trial of MB-CART19.1 in patients with relapsed or refractory CD19 positive B cell malignancies. | |||||||||||||||||||||||||||||||||
Medical condition: Pediatric and adult patients with relapsed/refractory (r/r) CD19-expressing B cell acute lymphoblastic leukemia (ALL) and Non-Hodgkin lymphoma (NHL), including chronic lymphocytic leukemia (CLL). | |||||||||||||||||||||||||||||||||
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Population Age: Infants and toddlers, Children, Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||||||||||||
Trial protocol: DE (Trial now transitioned) | |||||||||||||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2015-002821-20 | Sponsor Protocol Number: CR-AIR-008 | Start Date*: 2015-10-01 | |||||||||||||||||||||||||||||||
Sponsor Name:Kiadis Pharma Netherlands B.V. | |||||||||||||||||||||||||||||||||
Full Title: An exploratory, open-label, multicenter study to evaluate the safety and efficacy of a two-dose regimen of ATIR101, a T-lymphocyte enriched leukocyte preparation depleted ex vivo of host alloreacti... | |||||||||||||||||||||||||||||||||
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) PT (Completed) HR (Completed) | |||||||||||||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2015-005399-12 | Sponsor Protocol Number: DKMS-16-01 | Start Date*: 2017-08-02 | ||||||||||||||||||||||||||
Sponsor Name:DKMS gemeinnützige GmbH | ||||||||||||||||||||||||||||
Full Title: A randomized controlled trial comparing outcome after hematopoietic cell transplantation from a partially matched unrelated versus haploidentical donor | ||||||||||||||||||||||||||||
Medical condition: Patients with high-risk AML, ALL or MDS which have to undergo allogenic transplantaion. | ||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||
Trial protocol: DE (Completed) | ||||||||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2016-004672-21 | Sponsor Protocol Number: CR-AIR-009 | Start Date*: 2017-06-15 | |||||||||||||||||||||||||||||||
Sponsor Name:Kiadis Pharma Netherlands B.V. | |||||||||||||||||||||||||||||||||
Full Title: A Phase III, multicenter, randomized controlled study to compare safety and efficacy of a haploidentical HSCT and adjunctive treatment with ATIR101, a T-lymphocyte enriched leukocyte preparation de... | |||||||||||||||||||||||||||||||||
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, Elderly | Gender: Male, Female | ||||||||||||||||||||||||||||||||
Trial protocol: BE (Completed) GB (GB - no longer in EU/EEA) DE (Prematurely Ended) ES (Completed) PT (Completed) NL (Prematurely Ended) HR (Completed) FR (Prematurely Ended) IT (Prematurely Ended) | |||||||||||||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2005-005384-28 | Sponsor Protocol Number: INT 42/03 | Start Date*: 2004-03-24 | |||||||||||
Sponsor Name:FONDAZIONE MICHELANGELO - AVANZAMENTO DELLO STUDIO E CURA DEI TUMORI | |||||||||||||
Full Title: Randomized study of high-dose chemotherapy plus rituximab (R-HDS) vs conventional chemotherapy with rituximab (R-FC) in chronic lymphocytic leukemia at high risk. | |||||||||||||
Medical condition: Chronic lymphocytic leukemia at high risk | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2011-005790-23 | Sponsor Protocol Number: N/A | Start Date*: 2012-07-17 | ||||||||||||||||||||||||||
Sponsor Name:Birmingham Children's Hospital NHS Foundation Trust | ||||||||||||||||||||||||||||
Full Title: Comparison of adrenal recovery following short and long-term glucocorticoid therapy. | ||||||||||||||||||||||||||||
Medical condition: Adrenal recovery following long and short term steroid treatment. | ||||||||||||||||||||||||||||
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Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | |||||||||||||||||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) | ||||||||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2006-004902-16 | Sponsor Protocol Number: | Start Date*: 2007-10-01 | |||||||||||||||||||||
Sponsor Name:Royal Bournemouth Hospital | |||||||||||||||||||||||
Full Title: A randomized phase II trial to determine whether the application of imiquimod cream to the vaccination site can improve the immune responsiveness to influenza vaccination in patients with untreated... | |||||||||||||||||||||||
Medical condition: Early stage (Binet stage A) Patients with chronic lymphocytic leukaemia and control group of age and sex matched healthy volunteers | |||||||||||||||||||||||
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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: 2020-005843-21 | Sponsor Protocol Number: KT-US-982-5968 | Start Date*: 2022-02-08 | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Sponsor Name:KITE PHARMA INC. | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Full Title: Long-term Follow-up Study for Participants of Kite Sponsored Interventional Studies Treated With Gene-Modified Cells | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Medical condition: B-cell malignancies and Acute Myeloid Leukemia | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Trial protocol: IT (Trial now transitioned) FR (Trial now transitioned) DE (Trial now transitioned) NL (Trial now transitioned) ES (Ongoing) | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Trial results: (No results available) |
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: 2011-005186-20 | Sponsor Protocol Number: 7965-012 | Start Date*: 2012-07-12 | |||||||||||
Sponsor Name:Schering-Plough Research Institute, a Division of Schering Corporation. | |||||||||||||
Full Title: A Phase 3 Study to Evaluate the Efficacy and Safety of Dinaciclib or Ofatumumab in Subjects with Refractory Chronic Lymphocytic Leukemia (CLL) | |||||||||||||
Medical condition: chronic lymphocytic leukemia (CLL) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: NO (Completed) CZ (Completed) SE (Completed) FI (Completed) LT (Prematurely Ended) LV (Completed) ES (Completed) HU (Completed) IT (Completed) PL (Prematurely Ended) BE (Prematurely Ended) GR (Completed) EE (Prematurely Ended) SK (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2016-000704-28 | Sponsor Protocol Number: GCP#05.01.020 | Start Date*: 2016-06-16 | ||||||||||||||||||||||||||
Sponsor Name:Gamida Cell Ltd | ||||||||||||||||||||||||||||
Full Title: A Multicenter, Randomized, Phase III Registration Trial of Transplantation of NiCord®, Ex Vivo Expanded, Umbilical Cord Blood-derived, Stem and Progenitor Cells, versus Unmanipulated Umbilical Cord... | ||||||||||||||||||||||||||||
Medical condition: High risk haematological malignancies | ||||||||||||||||||||||||||||
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Population Age: Adolescents, Under 18, Adults | Gender: Male, Female | |||||||||||||||||||||||||||
Trial protocol: ES (Completed) NL (Completed) GB (GB - no longer in EU/EEA) IT (Prematurely Ended) PT (Completed) FR (Completed) | ||||||||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2013-003604-39 | Sponsor Protocol Number: MC-FludT.17/M | Start Date*: 2014-04-11 | ||||||||||||||||||||||||||
Sponsor Name:medac GmbH | ||||||||||||||||||||||||||||
Full Title: Clinical phase II trial to describe the safety and efficacy of Treosulfan-based conditioning therapy prior to allogeneic haematopoietic stem cell transplantation in paediatric patients with haemato... | ||||||||||||||||||||||||||||
Medical condition: Male and female children with haematologic malignant diseases as acute lymphoblastic leukaemias (ALL), acute myeloid leukaemias (AML), myelodysplastic syndromes (MDS) and juvenile myelomonocytic le... | ||||||||||||||||||||||||||||
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Population Age: Infants and toddlers, Children, Adolescents, Under 18 | Gender: Male, Female | |||||||||||||||||||||||||||
Trial protocol: DE (Completed) PL (Completed) AT (Completed) CZ (Completed) GB (Completed) IT (Completed) | ||||||||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2007-007612-29 | Sponsor Protocol Number: UCL/09/0050 | Start Date*: 2013-02-26 | |||||||||||
Sponsor Name:University College London | |||||||||||||
Full Title: Immunotherapy with CD19ζ chimeric antigen receptor gene-modified EBV-specific CTLs after stem cell transplant in children with high-risk acute lymphoblastic leukaemia | |||||||||||||
Medical condition: The medical condition under investigation is childhood precursor B acute lymphoblastic leukaemia (ALL). | |||||||||||||
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Population Age: Infants and toddlers, Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) GB (Completed) | |||||||||||||
Trial results: View results |
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: 2021-004450-36 | Sponsor Protocol Number: MK-2140-006 | Start Date*: 2022-06-10 | ||||||||||||||||||||||||||
Sponsor Name:Merck Sharp & DohmeLLC | ||||||||||||||||||||||||||||
Full Title: A Multicenter, Open-label, Phase 2 Basket Study to Evaluate the Safety and Efficacy of MK-2140 as a Monotherapy and in Combination in Participants with Aggressive and Indolent B-cell Malignancies (... | ||||||||||||||||||||||||||||
Medical condition: Aggressive and Indolent B-cell Malignancies | ||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||
Trial protocol: SE (Trial now transitioned) DE (Trial now transitioned) EE (Trial now transitioned) ES (Ongoing) PL (Trial now transitioned) CZ (Trial now transitioned) IE (Trial now transitioned) PT (Trial now transitioned) IT (Trial now transitioned) | ||||||||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2014-003124-44 | Sponsor Protocol Number: DKMS-14-01 | Start Date*: 2015-01-15 | ||||||||||||||||
Sponsor Name:DKMS gemeinnützige GmbH | ||||||||||||||||||
Full Title: Evaluation of the impact of remission induction chemotherapy prior to allogeneic stem cell transplantation in relapsed and poor-response patients with AML | ||||||||||||||||||
Medical condition: | ||||||||||||||||||
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Population Age: Adults | Gender: Male, Female | |||||||||||||||||
Trial protocol: DE (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2016-004356-30 | Sponsor Protocol Number: PCYC-1145-LT | Start Date*: 2020-03-11 | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Sponsor Name:Pharmacyclics Switzerland GmbH, an AbbVie company | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Full Title: Extended treatment protocol for subjects continuing to benefit from ibrutinib after completion of ibrutinib clinical trials | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Medical condition: | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) FR (Trial now transitioned) GR (Completed) CZ (Trial now transitioned) DE (Completed) ES (Ongoing) PL (Trial now transitioned) BE (Completed) HU (Trial now transitioned) IT (Trial now transitioned) | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2007-001626-27 | Sponsor Protocol Number: CC-5013-CLL-002 | Start Date*: 2009-04-14 | |||||||||||
Sponsor Name:Celgene Corporation | |||||||||||||
Full Title: A PHASE 3, MULTICENTER, RANDOMIZED, DOUBLE-BLIND, PLACEBO-CONTROLLED, PARALLEL-GROUP STUDY OF THE EFFICACY AND SAFETY OF LENALIDOMIDE (REVLIMID®) AS MAINTENANCE THERAPY FOR PATIENTS WITH B-CELL CHR... | |||||||||||||
Medical condition: Relapsed or refractory B-cell chronic lymphocytic leukemia (CLL) who have achieved at least partial response (PR) to second-line therapy. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) DE (Completed) BE (Completed) ES (Completed) HU (Completed) CZ (Completed) PT (Completed) AT (Completed) IT (Completed) DK (Completed) FR (Completed) SE (Completed) NL (Completed) IE (Completed) BG (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2018-004869-14 | Sponsor Protocol Number: CLL19H1 | Start Date*: 2019-04-15 | |||||||||||
Sponsor Name:Dept. of hematology, Herlev Hospital | |||||||||||||
Full Title: Peptide vaccination with PD-L1 and PD-L2 peptides in untreated chronic lymphatic leukemia. | |||||||||||||
Medical condition: Chronic lymphocytic leukemia with un-mutated IGHV | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2009-017376-25 | Sponsor Protocol Number: MEK111759 | Start Date*: 2011-03-15 | |||||||||||
Sponsor Name:GlaxoSmithKline Research & Development Ltd | |||||||||||||
Full Title: An Open-Label, Dose-Escalation, Phase I/II Study to Investigate the Safety, Pharmacokinetics, Pharmacodynamics and Clinical Activity of the MEK Inhibitor GSK1120212 in Subjects with Relapsed or Ref... | |||||||||||||
Medical condition: Relapsed or refractory leukemias | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Completed) DE (Completed) | |||||||||||||
Trial results: View results |
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