- Trials with a EudraCT protocol (54)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
54 result(s) found for: Lymphomas non-Hodgkin's unspecified histology.
Displaying page 1 of 3.
| EudraCT Number: 2016-003408-29 | Sponsor Protocol Number: 5F9003 | Start Date*: 2019-11-04 | ||||||||||||||||||||||||||||||||||||||||||||||
| Sponsor Name:Gilead Sciences, Inc. | ||||||||||||||||||||||||||||||||||||||||||||||||
| Full Title: A Phase 1b/2 Trial of Hu5F9-G4 in Combination with Rituximab or Rituximab + Chemotherapy in Patients with Relapsed/Refractory B-cell Non-Hodgkin’s Lymphoma | ||||||||||||||||||||||||||||||||||||||||||||||||
| Medical condition: Relapsed/Refractory B-cell Non-Hodgkin's Lymphoma. | ||||||||||||||||||||||||||||||||||||||||||||||||
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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: 2018-000929-32 | Sponsor Protocol Number: JCAR017-BCM-003 | Start Date*: 2018-08-21 | ||||||||||||||||
| Sponsor Name:Celgene Corporation | ||||||||||||||||||
| Full Title: A global randomized multicenter Phase 3 trial to compare the efficacy and safety of JCAR017 to standard of care in adult subjects with high-risk, transplant-eligible relapsed or refractory aggressi... | ||||||||||||||||||
| Medical condition: Transplant-eligible relapsed or refractory (R/R) aggressive B-cell Non Hodgkin Lymphoma (B-NHL) | ||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
| Trial protocol: FR (Completed) BE (Completed) ES (Ongoing) GB (GB - no longer in EU/EEA) SE (Completed) NL (Ongoing) IT (Completed) | ||||||||||||||||||
| Trial results: View results | ||||||||||||||||||
| EudraCT Number: 2010-019248-37 | Sponsor Protocol Number: IILINFL09 | Start Date*: 2010-12-30 | |||||||||||
| Sponsor Name:FONDAZIONE ITALIANA LINFOMI ONLUS | |||||||||||||
| Full Title: A Phase II study of Bendamustine in Combination With Rituximab as Initial Treatment for Patients With Indolent non-follicular Non-Hodgkin’s Lymphoma | |||||||||||||
| Medical condition: Patients with advanced untreated Indolent non Follicular non-Hodgkin Lymphomas | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: IT (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2004-002733-39 | Sponsor Protocol Number: ML18324 | Start Date*: 2005-04-06 | |||||||||||
| Sponsor Name:ROCHE | |||||||||||||
| Full Title: FC + rituximab followed by rituximab maintenance treatment in patients with advanced untreated Indolent B-cell Non follicular Lymphomas: phase II study. | |||||||||||||
| Medical condition: Previously untreated CD20-positive B-cell advanced indolent non follicular non-Hodgkin Lymphoma (NHL). | |||||||||||||
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| Population Age: Adults | Gender: Male, Female | ||||||||||||
| Trial protocol: IT (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2016-004718-90 | Sponsor Protocol Number: UTX-TGR-205 | Start Date*: 2017-10-10 | ||||||||||||||||||||||||||||||||||||||||||||||
| Sponsor Name:TG Therapeutics | ||||||||||||||||||||||||||||||||||||||||||||||||
| Full Title: A Phase 2b Randomized Study to Assess the Efficacy and Safety of the Combination of Ublituximab + TGR-1202 with or without Bendamustine and TGR-1202 alone in Patients with Previously Treated Non-Ho... | ||||||||||||||||||||||||||||||||||||||||||||||||
| Medical condition: Non-Hodgkin lymphoma | ||||||||||||||||||||||||||||||||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||||||||||||||||||||||
| Trial protocol: GB (GB - no longer in EU/EEA) PL (Prematurely Ended) SK (Prematurely Ended) ES (Prematurely Ended) IT (Prematurely Ended) | ||||||||||||||||||||||||||||||||||||||||||||||||
| Trial results: View results | ||||||||||||||||||||||||||||||||||||||||||||||||
| EudraCT Number: 2012-005157-23 | Sponsor Protocol Number: DART | Start Date*: 2013-05-21 | ||||||||||||||||||||||||||
| Sponsor Name:Fondazione IRCCS Istituto Nazionale Tumori | ||||||||||||||||||||||||||||
| Full Title: A Phase I/II Study of Danusertib in Combination with Romidepsin in Adult Patients with Mature Peripheral T Cell Lymphoma (PTCL) | ||||||||||||||||||||||||||||
| Medical condition: (Ph I) Relapsed or refractory Hodgkin (HL) and Non Hodgkin lymphoma (NHL) in patients in the absence, unable ot who have been refused to undergo alternative salvage regimens. (Ph II) Relapsed or r... | ||||||||||||||||||||||||||||
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| Population Age: Adults | Gender: Male, Female | |||||||||||||||||||||||||||
| Trial protocol: IT (Completed) | ||||||||||||||||||||||||||||
| Trial results: View results | ||||||||||||||||||||||||||||
| EudraCT Number: 2004-004082-15 | Sponsor Protocol Number: NILG-DC01-04 | Start Date*: 2004-11-09 | |||||||||||
| Sponsor Name:AZIENDA OSPEDALIERA "OSPEDALI RIUNITI DI BERGAMO" (A.O. DI RILIEVO NAZIONALE) | |||||||||||||
| Full Title: A PHASE II CLINICAL STUDY TO DETERMINE THE EFFICACY AND SAFETY OF DEPOCITE (CITARABINE LIPOSOMIALE INJECTON) FOR THE TREATMENT OF CNS RELAPSE IN ADULT PATIENTS WITH ACUTE LYMPOBLASTIC LEUKEMIA OR V... | |||||||||||||
| Medical condition: CNS RELAPSE IN ADULT PATIENT'S WITH ACUTE LYPHOBLASTIC LEUKEMIA O VERY AGGRESSIVE LYMPHOMA | |||||||||||||
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| Population Age: Adults | Gender: Male, Female | ||||||||||||
| Trial protocol: IT (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2013-003093-27 | Sponsor Protocol Number: PCI-32765FLR3001 | Start Date*: 2013-12-18 | |||||||||||
| Sponsor Name:Janssen-Cilag International NV | |||||||||||||
| Full Title: A Randomized, Double-blind, Placebo-controlled Phase 3 Study of the Bruton's Tyrosine Kinase Inhibitor, PCI-32765 (Ibrutinib), in Combination with Either Bendamustine and Rituximab (BR) or Rituxim... | |||||||||||||
| Medical condition: Indolent Non-Hodgkin Lymphoma (iNHL) | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: SE (Completed) BE (Completed) GB (GB - no longer in EU/EEA) ES (Ongoing) IT (Completed) DE (Completed) PL (Completed) FR (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2014-002226-13 | Sponsor Protocol Number: 2014011723 | Start Date*: 2014-11-26 | ||||||||||||||||||||||||||
| Sponsor Name:Rigshospitalet | ||||||||||||||||||||||||||||
| Full Title: A multimodality imaging approach for early detection and prediction of cardiotoxicity in Doxorubicin-treated patients with malignant lymphom | ||||||||||||||||||||||||||||
| Medical condition: Hodgkin and non-Hodgkin lymphoma | ||||||||||||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||
| Trial protocol: DK (Prematurely Ended) | ||||||||||||||||||||||||||||
| Trial results: (No results available) | ||||||||||||||||||||||||||||
| EudraCT Number: 2017-000106-38 | Sponsor Protocol Number: JCAR017-BCM-001 | Start Date*: 2018-06-14 | ||||||||||||||||
| Sponsor Name:Celgene Corporation | ||||||||||||||||||
| Full Title: A Phase 2, Single-arm, Multi-cohort, Multi-center Trial to Determine the Efficacy and Safety of JCAR017 in Adult Subjects with Aggressive B-Cell Non-Hodgkin Lymphoma (TRANSCEND WORLD) | ||||||||||||||||||
| Medical condition: Aggressive B-cell Non Hodgkin Lymphoma (B-NHL) | ||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
| Trial protocol: BE (Completed) FR (Completed) FI (Completed) ES (Restarted) DE (Completed) AT (Completed) NL (Ongoing) GB (Temporarily Halted) IT (Completed) | ||||||||||||||||||
| Trial results: View results | ||||||||||||||||||
| EudraCT Number: 2008-005859-16 | Sponsor Protocol Number: NHL 7-2008 | Start Date*: 2009-02-27 |
| Sponsor Name:StiL Forschungs-GmbH | ||
| Full Title: Prospective randomized Multicenter study in first-line treatment of Advanced progredIeNT follicular And other IndoleNt and mantle cell lymphomas | ||
| Medical condition: Indolent Non-Hodgkin Lymphomas, in particular follicular lymphomas, as well as marginal zone lymphomas, immunocytomas (Waldenström’s macroglobulinaemia) and mantle cell lymphomas | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: DE (Completed) AT (Completed) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2021-000493-29 | Sponsor Protocol Number: CA224-069 | Start Date*: 2022-05-20 | |||||||||||||||||||||
| Sponsor Name:BRISTOL-MYERS SQUIBB INTERNATIONAL CORPORATION | |||||||||||||||||||||||
| Full Title: A Phase 1/2 Study of the Safety, Tolerability, Pharmacokinetics and Preliminary Efficacy of Relatlimab Plus Nivolumab in Pediatric and Young Adult Participants with Recurrent or Refractory Classica... | |||||||||||||||||||||||
| Medical condition: Recurrent or Refractory Classical Hodgkin Lymphoma and Non-Hodgkin Lymphoma | |||||||||||||||||||||||
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| Population Age: Children, Adolescents, Under 18, Adults | Gender: Male, Female | ||||||||||||||||||||||
| Trial protocol: IT (Trial now transitioned) ES (Ongoing) NL (Trial now transitioned) | |||||||||||||||||||||||
| Trial results: (No results available) | |||||||||||||||||||||||
| EudraCT Number: 2015-004033-28 | Sponsor Protocol Number: IPI-145-22 | Start Date*: 2016-05-04 | |||||||||||
| Sponsor Name:Infinity Pharmaceuticals, Inc. | |||||||||||||
| Full Title: A Phase 3, Randomized, Double-blind Study of Duvelisib Administered in Combination with Rituximab and Bendamustine vs Placebo Administered in Combination with Rituximab and Bendamustine in Subjects... | |||||||||||||
| Medical condition: Indolent Non-Hodgkin Lymphoma | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: HU (Prematurely Ended) FI (Prematurely Ended) DE (Prematurely Ended) PT (Prematurely Ended) AT (Prematurely Ended) PL (Prematurely Ended) ES (Prematurely Ended) FR (Prematurely Ended) EE (Prematurely Ended) IT (Prematurely Ended) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2006-003657-24 | Sponsor Protocol Number: BRIL06 | Start Date*: 2006-09-06 | |||||||||||
| Sponsor Name:GIMURELL | |||||||||||||
| Full Title: A PHASE II MULTICENTER NON-RANDOMIZED STUDY TO ASSESS SAFETY, TOXICITY AND CLINICAL ACTIVITY OF THE ASSOCIATION OF BORTEZOMID VELCADE WITH RITUXIMAB IN RELAPSED/REFRACTORY INDOLENT NON FOLLICULAR... | |||||||||||||
| Medical condition: relapsed non follicular non-Hodgkin s Lymphoma | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: IT (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2004-000243-23 | Sponsor Protocol Number: Hx-CD4-109 | Start Date*: 2004-08-03 | |||||||||||
| Sponsor Name:Genmab A/S | |||||||||||||
| Full Title: An Open-Label Therapeutic Exploratory Clinical Trial of HuMax-CD4, a Fully Human Monoclonal Anti-CD4 Antibody, in Patients with refractory or relapsed Non-Cutaneous CD4+ T-Cell Lymphoma | |||||||||||||
| Medical condition: The mature non-cutaneous T-cell lymphomas expressing the CD4 molecule are the object of this protocol. 1.Peripheral T-cell lymphoma (PTCL) unspecified 2.Angioimmunnoblastic T-cell lymphoma 3.Anapl... | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: SE (Completed) DK (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2014-004544-36 | Sponsor Protocol Number: 1301.6 | Start Date*: 2015-07-13 | |||||||||||
| Sponsor Name:Boehringer Ingelheim International GmbH | |||||||||||||
| Full Title: A Phase III, randomized, double-blind, multi-center, multi-national trial to evaluate efficacy and safety of BI 695500 versus rituximab as a first-line immunotherapy treatment in patients with low ... | |||||||||||||
| Medical condition: Low tumor burden follicular lymphoma | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: BE (Completed) ES (Prematurely Ended) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2013-003561-34 | Sponsor Protocol Number: PCYC-1121-CA | Start Date*: 2014-01-07 | |||||||||||
| Sponsor Name:Pharmacyclics LLC | |||||||||||||
| Full Title: A Multicenter, Open-Label, Phase 2 Study of the Bruton’s Tyrosine Kinase (BTK) Inhibitor, Ibrutinib, in Subjects with Relapsed/Refractory Marginal Zone Lymphoma | |||||||||||||
| Medical condition: Relapsed or refractory marginal zone lymphoma | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: BE (Completed) DE (Completed) GB (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2008-001635-34 | Sponsor Protocol Number: 3129K7-2001-WW | Start Date*: 2009-05-21 | |||||||||||
| Sponsor Name:Wyeth Research Division of Wyeth Pharmaceuticals Inc., Clinical Research & Development | |||||||||||||
| Full Title: A Phase 2 Study of Inotuzumab Ozogamicin (CMC-544) in Subjects With Indolent Non-Hodgkin’s Lymphoma (NHL) That is Refractory to or has Relapsed After Rituximab and Chemotherapy or Radioimmunotherapy | |||||||||||||
| Medical condition: Indolent Non-Hodgkin's Lymphoma | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: HU (Completed) DE (Prematurely Ended) BE (Completed) NL (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2017-000719-17 | Sponsor Protocol Number: PIVeR | Start Date*: 2018-03-05 | |||||||||||
| Sponsor Name:LYSARC | |||||||||||||
| Full Title: A multicentre, phase II, open label, single arm study of pixantrone in patients with CD20-positive relapsed or refractory aggressive non-Hodgkin lymphoma treated with rituximab, ifosfamide and etop... | |||||||||||||
| Medical condition: Patients with CD20-positive relapsed or refractory aggressive non-Hodgkin lymphoma | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: FR (Completed) BE (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2017-001912-13 | Sponsor Protocol Number: KTE-C19-105 | Start Date*: 2018-04-24 | |||||||||||
| Sponsor Name:Kite Pharma, Inc. | |||||||||||||
| Full Title: A Phase 2 Multicenter Study of Axicabtagene Ciloleucel in Subjects with Relapsed/Refractory Indolent Non-Hodgkin Lymphoma (iNHL) (ZUMA-5) | |||||||||||||
| Medical condition: Relapsed or Refractory Indolent Non-Hodgkin Lymphoma (r/r) iNHL. | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: FR (Trial now transitioned) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
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