- Trials with a EudraCT protocol (169)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
169 result(s) found for: Hodgkins Lymphoma.
Displaying page 7 of 9.
EudraCT Number: 2012-002659-41 | Sponsor Protocol Number: MOR208C201 | Start Date*: 2012-12-17 | |||||||||||
Sponsor Name:MorphoSys AG | |||||||||||||
Full Title: A Phase IIa, Open-Label, Multicenter Study of Single-Agent MOR00208, an Fc-Optimized Anti-CD19 Antibody, in Patients with Relapsed or Refractory B-Cell Non-Hodgkin’s Lymphoma | |||||||||||||
Medical condition: Relapsed or Refractory B-Cell Non-Hodgkin’s Lymphoma | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Completed) IT (Completed) HU (Completed) ES (Completed) DE (Completed) PL (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2005-004442-14 | Sponsor Protocol Number: PEG UD0405 | Start Date*: 2005-12-06 | |||||||||||
Sponsor Name:UNIVERSITA' DEGLI STUDI DI UDINE | |||||||||||||
Full Title: A pilot clinical trial to evaluate the ability of pegylate r-metHg-CSF (Pegilgrastim) to accelerate haematology recovery of patients with Non-Hodgkins Lymphoma after High-dose chemiotherapy and aut... | |||||||||||||
Medical condition: Patients with - risk Non-Hodgkin's Lymphoma in complete or partial response who underwent autologous PBPC transplantation after high-dose chemiotherapy. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2007-001657-26 | Sponsor Protocol Number: KCH-BMT-07-1.0 | Start Date*: 2008-02-29 | ||||||||||||||||||||||||||||||||||||||||||||||
Sponsor Name:King's College Hospital NHS Foundation Trust | ||||||||||||||||||||||||||||||||||||||||||||||||
Full Title: Single Centre Phase II Pilot study of Unrelated Cord Blood Transplantation in Patients with Poor Risk Haematological Malignancies. | ||||||||||||||||||||||||||||||||||||||||||||||||
Medical condition: 1. Acute, chronic leukaemia or myelodysplastic syndrome for which allogeneic transplantation is considered as the best treatment option. 2. Acute lymphoblastic leukaemia (ALL) 3. Non-Hodgkin’s l... | ||||||||||||||||||||||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||||||||||||||||||||||
Trial protocol: GB (Completed) | ||||||||||||||||||||||||||||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2006-005159-14 | Sponsor Protocol Number: GC P#02.01.001 | Start Date*: 2008-04-15 | |||||||||||||||||||||||||||||||||||||||||
Sponsor Name:Gamida Cell-Teva Joint Venture Ltd. | |||||||||||||||||||||||||||||||||||||||||||
Full Title: A Multi-Center, Multi-National, Historical Cohort Controlled Study to Evaluate Efficacy and Safety of Transplantation of StemEx, Umbilical Cord Blood Stem and Progenitor Cells Expanded Ex Vivo, in ... | |||||||||||||||||||||||||||||||||||||||||||
Medical condition: High-risk haematological malignancies (including AML, ALL, CML, NHL, HD, and MDS) with an indication for allogeneic haematopoietic stem cell transplantation, to support haematopoietic reconstitutio... | |||||||||||||||||||||||||||||||||||||||||||
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Population Age: Adolescents, Under 18, Adults | Gender: Male, Female | ||||||||||||||||||||||||||||||||||||||||||
Trial protocol: ES (Completed) IT (Completed) HU (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: 2004-000607-17 | Sponsor Protocol Number: SG030-0003 | Start Date*: 2004-09-30 | |||||||||||
Sponsor Name:Seattle Genetics, Inc. | |||||||||||||
Full Title: A Phase II Multi-Dose Study of SGN-30 (anti-CD30 mAb) in Patients with Refractory or Recurrent Hodgkin’s Disease or Anaplastic Large Cell Lymphoma | |||||||||||||
Medical condition: Refractory or Recurrent Hodgkin’s Disease or Anaplastic Large Cell Lymphoma MedDRA version 6.0 PT=Hodgkin's Disease NOS recurrent=10020256 PT=Hodgkin's Disease NOS refractory=10020257 PT=Anaplast... | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: SE (Completed) DK (Completed) BE (Completed) IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2021-004324-14 | Sponsor Protocol Number: WU-CART-007-1001 | Start Date*: 2023-06-26 | ||||||||||||||||
Sponsor Name:Wugen, Inc. | ||||||||||||||||||
Full Title: A Phase 1/2 Dose-Escalation and Dose-Expansion Study of the Safety and Efficacy of Anti-CD7 Allogeneic CAR-T cells (WU-CART-007) in Patients with Relapsed or Refractory T-cell Acute Lymphoblastic L... | ||||||||||||||||||
Medical condition: Relapsed or Refractory T-cell Acute Lymphoblastic Leukemia | ||||||||||||||||||
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Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: FR (Completed) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2018-000356-18 | Sponsor Protocol Number: NL64877.041.18 | Start Date*: 2018-11-19 | |||||||||||||||||||||||||||||||||||||||||
Sponsor Name:University Medical Center utrecht | |||||||||||||||||||||||||||||||||||||||||||
Full Title: Individualized dosing of fludarabine during innate allo SCT: A randomized phase II study (TARGET Study) | |||||||||||||||||||||||||||||||||||||||||||
Medical condition: AML, MDS, ALL, CML, CLL, NHL, HL, or a myeloproliferative disease (MPD) | |||||||||||||||||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||||||||||||||||||||||
Trial protocol: NL (Completed) | |||||||||||||||||||||||||||||||||||||||||||
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: 2019-002419-24 | Sponsor Protocol Number: RG_19-116 | Start Date*: 2020-09-23 | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Sponsor Name:The University of Birmingham | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Full Title: A multi-centre phase II trial of GvHD prophylaxis following unrelated donor stem cell transplantation comparing Thymoglobulin vs. Calcineurin inhibitor or Sirolimus-based post-transplant cyclophosp... | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Medical condition: Acute Myeloid Leukaemia, Acute lymphoblastic leukaemia, Chronic myelomonocytic leukemia, Myelodysplastic syndromes, Non-Hodgkin lymphoma, Hodgkin lymphoma, Multiple myeloma, Chronic lymphocytic leu... | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
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Population Age: Under 18, Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2016-002654-21 | Sponsor Protocol Number: RHMCAN1219 | Start Date*: 2017-11-23 | |||||||||||
Sponsor Name:University Hospital Southampton NHS Foundation Trust | |||||||||||||
Full Title: A PHASE II STUDY OF ATEZOLIZUMAB WITH RITUXIMAB, GEMCITABINE AND OXALIPLATIN IN PATIENTS WITH RELAPSED OR REFRACTORY DIFFUSE LARGE B-CELL LYMPHOMA WHO ARE NOT CANDIDATES FOR HIGH-DOSE THERAPY. | |||||||||||||
Medical condition: Diffuse large B-cell lymphoma (most common type of non-Hodgkins lymphoma) | |||||||||||||
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Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) | |||||||||||||
Trial results: View results |
EudraCT Number: 2015-003213-18 | Sponsor Protocol Number: RHMCAN1129 | Start Date*: 2017-01-13 | |||||||||||
Sponsor Name:University Hospital Southampton NHS Foundation Trust | |||||||||||||
Full Title: A Phase Ib/II combination trial of acalabrutinib with rituximab, cyclophosphamide, doxorubicin,vincristine and prednisolone (R-CHOP) for patients with diffuse large B-cell lymphoma (DLBCL) | |||||||||||||
Medical condition: Diffuse large B-cell lymphomas (most common type of non-Hodgkins lymphoma) | |||||||||||||
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Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2007-004092-19 | Sponsor Protocol Number: EuroNet-PHL-LP1 | Start Date*: 2009-07-22 | |||||||||||
Sponsor Name:Martin Luther University of Halle/Wittenberg | |||||||||||||
Full Title: EuroNet-Paediatric Hodgkin’s Lymphoma Group First international Inter-Group Study for nodular lymphocyte-predominant Hodgkin’s Lymphoma in Children and Adolescents | |||||||||||||
Medical condition: The first line therapy for childhood nodular lymphocyte-predominant Hodgkin’s lymphoma shall be further optimised to avoid over-treatment and decrease long-term complications. | |||||||||||||
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Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) CZ (Completed) AT (Completed) NL (Ongoing) GB (GB - no longer in EU/EEA) FR (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2007-000219-27 | Sponsor Protocol Number: 3129K4-3301-WW | Start Date*: 2008-04-25 | |||||||||||
Sponsor Name:Wyeth Pharmaceuticals Inc. acting through its division Wyeth Research, a Pfizer Company | |||||||||||||
Full Title: An Open-Label, Randomized, Phase 3 Study of Inotuzumab Ozogamicin (CMC-544) Administered in Combination With Rituximab Compared to a Defined Investigator’s Choice Therapy in Subjects With Relapsed ... | |||||||||||||
Medical condition: Relapsed or refractory, CD22-Positive, follicular B-cell Non Hodgkin's Lymphoma | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Completed) ES (Completed) PT (Prematurely Ended) DE (Completed) FR (Completed) GB (Completed) IE (Completed) IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2007-004888-22 | Sponsor Protocol Number: CHCD122A2103 | Start Date*: 2008-03-27 |
Sponsor Name:Novartis Pharma AG | ||
Full Title: A phase IA/II, multi-center, open-label study of HCD122 administered intravenously once weekly for four weeks in adult patients with advanced non-Hodgkin's or Hodgkin's lymphoma who have progressed... | ||
Medical condition: Advanced non Hodgkin's or Hodgkin's lymphoma | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: BE (Completed) DE (Completed) FR (Completed) GB (Completed) | ||
Trial results: View results |
EudraCT Number: 2014-000576-26 | Sponsor Protocol Number: BO29337 | Start Date*: 2014-11-04 | |||||||||||
Sponsor Name:AbbVie Deutschland GmbH & Co. KG | |||||||||||||
Full Title: A PHASE II, OPEN-LABEL STUDY EVALUATING THE SAFETY AND EFFICACY OF GDC-0199 (ABT- 199) PLUS BENDAMUSTINE PLUS RITUXIMAB (BR) IN COMPARISON WITH BR ALONE OR GDC-0199 PLUS RITUXIMAB (R) IN PATIENTS W... | |||||||||||||
Medical condition: Relapsed and refractory follicular non-Hodgkins Lymphoma (R/R FL) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) IT (Completed) DE (Completed) BE (Completed) FR (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2009-012807-25 | Sponsor Protocol Number: IIL-MCL0208 | Start Date*: 2010-01-28 | ||||||||||||||||||||||||||
Sponsor Name:IIL INTERGRUPPO ITALIANO LINFOMI ONLUS | ||||||||||||||||||||||||||||
Full Title: A PHASE III MULTICENTER, RANDOMIZED STUDY WITH LENALIDOMIDE (Revlimid) MAINTENANCE VERSUS OBSERVATION AFTER INTENSIFIED INDUCTION REGIMEN CONTAINING RITUXIMAB FOLLOWED BY HIGH DOSE CHEMOTHERAPY A... | ||||||||||||||||||||||||||||
Medical condition: Mantel cell lymphoma | ||||||||||||||||||||||||||||
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Population Age: Adults | Gender: Male, Female | |||||||||||||||||||||||||||
Trial protocol: IT (Completed) PT (Completed) | ||||||||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2018-002556-32 | Sponsor Protocol Number: ADCT-301-201 | Start Date*: 2019-12-16 | |||||||||||||||||||||||||||||||
Sponsor Name:ADC Therapeutics SA | |||||||||||||||||||||||||||||||||
Full Title: A Phase 2, Open-Label, Single-Arm Study to Evaluate the Efficacy and Safety of Camidanlumab Tesirine (ADCT-301) in Patients with Relapsed or Refractory Hodgkin Lymphoma | |||||||||||||||||||||||||||||||||
Medical condition: Relapsed or Refractory Hodgkin Lymphoma | |||||||||||||||||||||||||||||||||
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Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||||||||||||
Trial protocol: DE (Completed) BE (Completed) PL (Completed) FR (Completed) CZ (Completed) HU (Completed) ES (Ongoing) GB (GB - no longer in EU/EEA) IT (Completed) | |||||||||||||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2019-001073-86 | Sponsor Protocol Number: MT-3724_NHL_001 | Start Date*: 2020-01-14 | ||||||||||||||||
Sponsor Name:Molecular Templates, Inc. | ||||||||||||||||||
Full Title: Safety, Pharmacodynamics and Efficacy of MT-3724 for the Treatment of Patients with Relapsed or Refractory DLBCL | ||||||||||||||||||
Medical condition: relapsed or refractory diffuse large B-cell lymphoma (DLBCL) | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: ES (Prematurely Ended) PL (Prematurely Ended) GB (GB - no longer in EU/EEA) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2014-003171-39 | Sponsor Protocol Number: T-Control | Start Date*: 2016-03-08 | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Sponsor Name:University Hospital Wuerzburg | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Full Title: Transfer of Streptamer-selected multi-antigen specific T cells to prevent infections and relapse and to reduce the risk of Graft-versus-Host Disease after allogeneic stem cell transplantation | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Medical condition: patients with hematological malignancies after T cell depleted allo-SCT | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Trial protocol: DE (Completed) | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Trial results: (No results available) |
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