- Trials with a EudraCT protocol (224)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
224 result(s) found for: Lymphatic Diseases AND Hodgkin Lymphoma.
Displaying page 1 of 12.
EudraCT Number: 2014-002251-26 | Sponsor Protocol Number: CL1-078454-018 | Start Date*: 2014-09-08 | |||||||||||||||||||||
Sponsor Name:Institut de Recherches Internationales Servier | |||||||||||||||||||||||
Full Title: Long-term safety study of abexinostat (S 078454) per os given as single-agent in haematological malignancies – Extension study | |||||||||||||||||||||||
Medical condition: Hodgkin's Disease (HD) , Non-Hodgkin Lymphoma (NHL) and Chronic Lymphocytic Leukaemia (CLL) | |||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: BE (Prematurely Ended) HU (Prematurely Ended) | |||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2015-003128-30 | Sponsor Protocol Number: Uni-Koeln-1776 | Start Date*: 2016-05-19 | |||||||||||
Sponsor Name:University of Cologne | |||||||||||||
Full Title: Phase II trial of the Btk-inhibitor Ibrutinib in patients with relapsed nodular lymphocyte-predominant Hodgkin Lymphoma (NLPHL) | |||||||||||||
Medical condition: relapsed lymphocyte-predominant Hodgkin lymphoma | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2016-002626-37 | Sponsor Protocol Number: Uni-Koeln-2854 | Start Date*: 2017-03-10 | |||||||||||
Sponsor Name:University of Cologne | |||||||||||||
Full Title: Nivolumab and AVD in earlystage unfavorable classical Hodgkin lymphoma - A GHSG randomized, multicenter phase II trial | |||||||||||||
Medical condition: Improvement of first-line treatment for early-stage unfavorable cHL by introduction of the anti-PD-1 antibody Nivolumab in combincation with a truncated standard chemotherapy (AVD). | |||||||||||||
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Population Age: | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2009-013691-47 | Sponsor Protocol Number: CL1-78454-001 | Start Date*: 2009-12-08 | |||||||||||||||||||||
Sponsor Name:Institut de Recherches Internationales Servier | |||||||||||||||||||||||
Full Title: Phase I/II dose-escalation study of oral administration of the Pan-Histone Deacetylase (HDAC) Inhibitor S 78454 in Hodgkin’s Disease, non-Hodgkin Lymphoma and Chronic Lymphocytic Leukaemia | |||||||||||||||||||||||
Medical condition: Hodgkin's disease (HD) , non-Hodgkin lymphoma (NHL) and chronic lymphocytic Leukaemia (CLL) | |||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: FR (Completed) GB (Completed) BE (Completed) HU (Completed) | |||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2013-003990-89 | Sponsor Protocol Number: Uni-Koeln-1707 | Start Date*: 2015-05-12 | |||||||||||
Sponsor Name:University of Cologne | |||||||||||||
Full Title: Brentuximab vedotin or B-CAP in the treatment of older patients with newly diagnosed classical Hodgkin Lymphoma – a GHSG-NLG Intergroup Phase II trial – | |||||||||||||
Medical condition: Treatment of older patients with newly diagnosed classical Hodgkin lymphoma | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) NO (Completed) SE (Completed) DK (Completed) FI (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2017-002444-32 | Sponsor Protocol Number: 17-122 | Start Date*: 2017-12-18 | |||||||||||
Sponsor Name:CHU CAEN | |||||||||||||
Full Title: Maintenance Brentuximab Vedotin (Bv) Following Allogeneic Stem Cell Transplantation for Hodgkin Lymphoma Patient: A Prospective, Multicenter, Phase II Study | |||||||||||||
Medical condition: Hodgkin Lymphoma Patients | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2007-003080-45 | Sponsor Protocol Number: BRD/07/005 | Start Date*: 2008-07-11 | |||||||||||
Sponsor Name:University College London | |||||||||||||
Full Title: Phase ll study evaluating the toxicity and efficacy of a modified German Paediatric Hodgkin's Lymphoma protocol (HD95) in young adults (aged 18-30 years) with Hodgkin's Lymphoma | |||||||||||||
Medical condition: Medical condition under investigation is known as Hodgkin's disease, which is a cancer of the lymphatic system. It is usually treated with either chemotherapy or radiotherapy or a combination of bo... | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2011-002810-35 | Sponsor Protocol Number: LEBEN | Start Date*: 2011-12-09 | |||||||||||
Sponsor Name:ISTITUTO NAZIONALE PER LO STUDIO E LA CURA DEI TUMORI - FONDAZIONE "G. PASCALE" | |||||||||||||
Full Title: A Phase 1/2 Study of Lenalidomide in combination with Bendamustine (LEBEN) in relapsed and primary refractory Hodgkin Lymphoma | |||||||||||||
Medical condition: relapsed and primary refractory Hodgkin Lymphoma | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2012-004246-15 | Sponsor Protocol Number: HIJAK | Start Date*: 2013-07-08 | |||||||||||
Sponsor Name:LYSARC | |||||||||||||
Full Title: A Phase II study of oral JAK1/JAK2 inhibitor INC424 in adult patients with relapsed/refractory classical Hodgkin’s lymphoma | |||||||||||||
Medical condition: Relapsed or refractory classical Hodgkin's lymphoma | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2017-003334-82 | Sponsor Protocol Number: Uni-Koeln-3140 | Start Date*: 2019-03-11 | |||||||||||
Sponsor Name:University of Cologne | |||||||||||||
Full Title: Abscopal Effect of Radiotherapy and Nivolumab in anti-PD1 Pretreated Relapsed or Refractory classical Hodgkin Lymphoma - An international multicenter Phase II trial | |||||||||||||
Medical condition: Improvement of efficacy of nivolumab in patients with relapsed or refractory classical Hodgkin Lymphoma who recently progressed on anti-PD1 therapy. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) NO (Completed) NL (Completed) AT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2010-021086-73 | Sponsor Protocol Number: Uni-Koeln-1443 | Start Date*: 2012-05-11 | |||||||||||
Sponsor Name:University of Cologne | |||||||||||||
Full Title: HD-R3i - A prospective, randomized, placebo-controlled, international, multicenter phase I/II trial of RAD001 (everolimus) in combination with DHAP as induction therapy in patients with relapsed or... | |||||||||||||
Medical condition: relapsed or refractory Hodgkin Lymphoma | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2015-001570-17 | Sponsor Protocol Number: LYMRIT-37-06 | Start Date*: 2015-09-14 | ||||||||||||||||
Sponsor Name:Nordic Nanovector ASA | ||||||||||||||||||
Full Title: A Phase 2 study of the antibody-radionuclide-conjugate 177Lu-DOTA-HH1 (Betalutin™) in patients with CD37-positive relapsed follicular lymphoma | ||||||||||||||||||
Medical condition: Relapsed CD37+ non-Hodgkin B-cell follicular lymphoma | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: HU (Prematurely Ended) ES (Prematurely Ended) AT (Completed) DK (Prematurely Ended) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2012-002012-46 | Sponsor Protocol Number: BV-ABVD | Start Date*: 2012-11-15 | |||||||||||
Sponsor Name:AZIENDA OSPEDALIERA POLICLINICO DI MODENA | |||||||||||||
Full Title: A pilot phase II study to assess the efficacy of Brentuximab Vedotin administered sequentally with ABVD chemotherapy in patients with untreated Hodgkin Lymphoma | |||||||||||||
Medical condition: Previously untreated patients with classical Hodgkin Lymphoma according to the World Health Organisation (WHO) classification | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2014-001509-42 | Sponsor Protocol Number: CA209-205 | Start Date*: 2014-07-11 | |||||||||||
Sponsor Name:Bristol-Myers Squibb International Corporation | |||||||||||||
Full Title: Non-Comparative, Multi-Cohort, Single Arm, Open-Label, Phase 2 Study of Nivolumab (BMS-936558) in classical Hodgkin Lymphoma (cHL) Subjects | |||||||||||||
Medical condition: Hodgkin Disease | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: AT (Completed) BE (Completed) DE (Completed) IT (Completed) NL (Completed) ES (Ongoing) CZ (Completed) GB (GB - no longer in EU/EEA) | |||||||||||||
Trial results: View results |
EudraCT Number: 2007-006064-30 | Sponsor Protocol Number: UCL/07/146 | Start Date*: 2008-04-09 | |||||||||||
Sponsor Name:University College London | |||||||||||||
Full Title: A randomised phase III trial to assess response adapted therapy using FDG-PET imaging in patients with newly diagnosed, advanced Hodgkin Lymphoma | |||||||||||||
Medical condition: Medical condition under investigation is Hodgkin Lymphoma, which is a cancer of the lymphatic system. It is usually treated with either chemotherapy or radiotherapy or a combination of both. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) IT (Ongoing) IE (Completed) SE (Completed) DK (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2016-002347-41 | Sponsor Protocol Number: CA209-744 | Start Date*: Information not available in EudraCT | |||||||||||
Sponsor Name:Bristol-Myers Squibb International Corporation | |||||||||||||
Full Title: Risk-based, response-adapted, Phase II open-label trial of nivolumab + brentuximab vedotin (N + Bv) for children, adolescents, and young adults with relapsed/refractory (R/R) CD30 + classic Hodgkin... | |||||||||||||
Medical condition: Relapsed/refractory (R/R) CD30 + classic Hodgkin lymphoma (cHL) | |||||||||||||
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Population Age: Children, Adolescents, Under 18, Adults | Gender: Male, Female | ||||||||||||
Trial protocol: CZ (Completed) ES (Ongoing) IE (Completed) DE (Completed) GB (GB - no longer in EU/EEA) NL (Completed) PL (Completed) Outside EU/EEA IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2016-002272-27 | Sponsor Protocol Number: DSHNHL2015-1 | Start Date*: 2017-04-06 | |||||||||||
Sponsor Name:Saarland University | |||||||||||||
Full Title: Improvement of Outcome in Elderly Patients or Patients not eligible for high-dose chemotherapy with Aggressive Non-Hodgkin Lymphoma in first Relapse or Progression by adding Nivolumab to Gemcitabin... | |||||||||||||
Medical condition: Patients with first relapse or progression of aggressive Non-Hodgkin’s Lymphoma who are not eligible neither for autologous nor allogeneic stem cell transplantation | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) FR (Completed) BE (Completed) NL (Ongoing) PL (Completed) AT (Completed) PT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2017-000498-35 | Sponsor Protocol Number: 1537 | Start Date*: 2019-03-12 | ||||||||||||||||||||||||||||||||||||
Sponsor Name:European Organisation for Research and Treatment of Cancer (EORTC) | ||||||||||||||||||||||||||||||||||||||
Full Title: Very early FDG-PET-response adapted targeted therapy for advanced Hodgkin lymphoma: a single-arm phase II study | ||||||||||||||||||||||||||||||||||||||
Medical condition: Advanced stage Hodgkin Lymphoma | ||||||||||||||||||||||||||||||||||||||
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Population Age: Adults | Gender: Male, Female | |||||||||||||||||||||||||||||||||||||
Trial protocol: DK (Trial now transitioned) BE (Trial now transitioned) PL (Trial now transitioned) SK (Trial now transitioned) ES (Ongoing) PT (Trial now transitioned) | ||||||||||||||||||||||||||||||||||||||
Trial results: (No results available) |
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: 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) |
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