- Trials with a EudraCT protocol (68)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
68 result(s) found for: Donor lymphocyte infusion.
Displaying page 1 of 4.
EudraCT Number: 2012-002418-38 | Sponsor Protocol Number: LUMC2012-01 | Start Date*: 2012-08-21 | |||||||||||
Sponsor Name:Leiden University Medical Center | |||||||||||||
Full Title: Prophylactic infusion of CD4 positive donor lymphocytes early after T-cell depleted allogeneic stem cell transplantation in patients with an unrelated donor | |||||||||||||
Medical condition: Patients with AML, MDS, ALL, CML in accelerated phase or blastic transformation, CLL, MM or aggressive lymphoma, who underwent a (non) myeloablative allo-SCT with an unrelated donor. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2012-003691-40 | Sponsor Protocol Number: LUMC2010-01 | Start Date*: 2012-09-19 |
Sponsor Name:Leiden University Medical Center | ||
Full Title: Administration of leukemia-reactive donor T cells after allogeneic stem cell transplantation or donor lymphocyte infusion to patients with persistent or relapsed mature B cell neoplasm with blood a... | ||
Medical condition: persistent or relapsed mature B cell neoplasm with blood and/or bone marrow involvement | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: NL (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2016-002077-35 | Sponsor Protocol Number: EC-HEM-HGUGM-2016-01 | Start Date*: 2017-05-05 |
Sponsor Name:José Luís Díez Martín | ||
Full Title: CLINICAL TRIAL PHASE I / II, SINGLE-CENTER, HISTORICAL CONTROL, TO EVALUATE THE EFFECTIVENESS OF DONOR IL-15-STIMULATED NK CELLS POST TRANSPLANT INFUSION, IN ACUTE LEUKEMIA PATIENTS WITH POOR PROGN... | ||
Medical condition: High risk acute myeloid leukemia | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: ES (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2013-004953-26 | Sponsor Protocol Number: BHS-TC13 | Start Date*: 2016-03-11 |
Sponsor Name:Ghent University Hospital | ||
Full Title: CMV specific T cell therapy for the treatment of relapsing or therapy refractory CMV infection after allogeneic stem cell transplantation with a CMV-positive donor. | ||
Medical condition: CMV specific T cell therapy for the treatment of relapsing or therapy refractory CMV infection after allogeneic stem cell transplantation with a CMV-positive donor. | ||
Disease: | ||
Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | |
Trial protocol: BE (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2011-001514-34 | Sponsor Protocol Number: ILNK15-01 | Start Date*: 2012-04-03 | |||||||||||
Sponsor Name:Leiden University Medical Center | |||||||||||||
Full Title: Infusion of IL-15 activated NK cells after allogeneic stem cell transplantation in children transplanted for relapsed/refractory leukemia: a feasibility study | |||||||||||||
Medical condition: Children with high-risk and recurrent acute leukemia are eligible for allogeneic hematopoietic stem cell transplantation (HSCT). However, leukemia relapse and viral infections after HSCT remain mai... | |||||||||||||
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Population Age: Infants and toddlers, Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2017-002314-31 | Sponsor Protocol Number: DLI-TARGET | Start Date*: 2018-08-20 | ||||||||||||||||
Sponsor Name:Klinikum der Universität München | ||||||||||||||||||
Full Title: Phase 2 Study Evaluating the Safety, Tolerability and Efficacy of Allogeneic Donor Lymphocyte Infusions Combined with Blinatumomab in Patients with Treatment-Resistant Mixed Chimerism or Minimal Re... | ||||||||||||||||||
Medical condition: Subjects with treatment-resistant mixed chimerism or MRD of CD19+ B-precursor ALL after allogeneic SCT | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: DE (Prematurely Ended) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2007-000210-36 | Sponsor Protocol Number: Euro-NHB | Start Date*: 2007-10-04 |
Sponsor Name:UMC St Radboud University Hospital Center | ||
Full Title: A prospective, randomized, open, multicenter study to evaluate the efficacy and tolerability of induction therapy with a single high-dose anti-T-lymphocyte globulin (ATG-Fresenius) in renal transpl... | ||
Medical condition: Transplantation of a renal graft from a non-heart-beating donor | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: NL (Prematurely Ended) | ||
Trial results: (No results available) |
EudraCT Number: 2019-002311-26 | Sponsor Protocol Number: INMUNOCELL | Start Date*: 2021-12-09 | |||||||||||||||||||||||||||||||
Sponsor Name:IDIVAL | |||||||||||||||||||||||||||||||||
Full Title: PROPHYLAXIS OF CYTOMEGALOVIRUS INFECTION IN haploidentical PROGENITORS HEMATOPOIETIC TRANSPLANTATIONWITH ADOPTIVE CELL IMMUNOTHERAPY. | |||||||||||||||||||||||||||||||||
Medical condition: Primary prophylaxis of CMV infection in haploidentical transplantation of hematopoietic progenitors. | |||||||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||||||||||||
Trial protocol: ES (Ongoing) | |||||||||||||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2016-002959-17 | Sponsor Protocol Number: CR-BD-001 | Start Date*: 2016-12-02 | |||||||||||
Sponsor Name:Kiadis Pharma Netherlands B.V. | |||||||||||||
Full Title: An exploratory, open-label study to evaluate the safety and feasibility of ATIR201, a T-lymphocyte enriched leukocyte preparation depleted ex vivo of host alloreactive T-cells (using photodynamic t... | |||||||||||||
Medical condition: Patients with beta-thalassemia major who are eligible for a haploidentical HSCT | |||||||||||||
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Population Age: Children, Adolescents, Under 18, Adults | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2020-000419-56 | Sponsor Protocol Number: TCD601B101 | Start Date*: 2021-03-23 | |||||||||||
Sponsor Name:ITB-MED AB | |||||||||||||
Full Title: A 12-month, randomized, controlled, open-label, dose escalation study evaluating safety, tolerability, pharmacokinetics (PK) and pharmacodynamics (PD) of an anti-CD2 monoclonal antibody, TCD601 (si... | |||||||||||||
Medical condition: renal transplantation | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: SE (Ongoing) AT (Trial now transitioned) ES (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2012-002435-28 | Sponsor Protocol Number: mHagDC | Start Date*: 2012-09-21 |
Sponsor Name:University Medical Center Utrecht | ||
Full Title: A phase I/II “minor histocompatibility antigen” (mHag)-based Dendritic cell vaccination trial after allogeneic Stem Cell Transplantation to improve the safety and efficacy of donor Lymphocyte infus... | ||
Medical condition: Low grade, intermediate and high grade non Hodgkin lymphoma (NHL), M.Hodgkin, Chronic Lymphocytic Leukemia (CLL), Chronic Myeloid Leukemia (CML), Acute Lymphoblastic Leukemia (ALL), Myelodysplasia ... | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: NL (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2011-002192-41 | Sponsor Protocol Number: E:531/2011 | Start Date*: 2012-02-09 |
Sponsor Name:University Hospital Tübingen | ||
Full Title: Multicenter phase II study of peritransplantation immunosuppression using ATG, rituximab, sirolimus and mycophenolate mofetil in patient receiving mismatched hematopoietic cell transplantation afte... | ||
Medical condition: Treatment of patient with advanced hematologic malignancies such as patients with leukemia or lymphoma treatable by allogeneic stem cell transplantation but without a suitable matched donor. | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: DE (Completed) | ||
Trial results: View results |
EudraCT Number: 2007-004517-34 | Sponsor Protocol Number: AMLSCT-BFM2007 | Start Date*: 2010-01-13 | ||||||||||||||||
Sponsor Name:Hannover Medical School | ||||||||||||||||||
Full Title: Allogeneic stem cell transplantation for children, adolescents and young adults with relapsed or refractory AML Multi Center Therapy Concept | ||||||||||||||||||
Medical condition: Relapsed or refractory Acute Myeloid Leukemia (AML) | ||||||||||||||||||
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Population Age: Infants and toddlers, Children, Adolescents, Under 18, Adults | Gender: Male, Female | |||||||||||||||||
Trial protocol: DE (Completed) CZ (Completed) AT (Completed) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2012-001188-55 | Sponsor Protocol Number: HOVON115 | Start Date*: 2012-07-10 | |||||||||||
Sponsor Name:HOVON Foundation | |||||||||||||
Full Title: Double umbilical cord blood transplantation in high-risk hematological patients. A phase II study focussing on the mechanism of graft predominance | |||||||||||||
Medical condition: Patients with high-risk hematological diseases, who need a allogeneic stem cell transplantation but who lack a matched unrelated donor | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Ongoing) BE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2021-000417-16 | Sponsor Protocol Number: Uni-Köln-4480 | Start Date*: 2021-10-20 | |||||||||||
Sponsor Name:University of Cologne | |||||||||||||
Full Title: A Phase I / randomized Phase II trial to analyse safety and efficacy of human SARS-CoV 2 specific T lymphocyte transfer in patients with COVID-19 in need of treatment or at risk of severe COVID-19 | |||||||||||||
Medical condition: Patients who are tested positive for SARS-CoV-2 by PCR from upper or lower respiratory sites and are at increased risk for developing critical disease presenting with moderate disease -WHO ordinal ... | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2014-004849-26 | Sponsor Protocol Number: Parachute04 | Start Date*: 2015-02-05 | ||||||||||||||||
Sponsor Name:UMC Utrecht | ||||||||||||||||||
Full Title: PARACHUTE-trial Prospective Analysis of an individualized dosing Regimen of ATG (Thymoglobulin) in Children Undergoing HCT: redUcing Toxicity and improving Efficacy – a single arm phase II study | ||||||||||||||||||
Medical condition: Leukemia and immunedeficiency syndromes | ||||||||||||||||||
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Population Age: Adolescents, Under 18 | Gender: Male, Female | |||||||||||||||||
Trial protocol: NL (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2008-004955-31 | Sponsor Protocol Number: UCL/08/0122 | Start Date*: 2009-08-14 | |||||||||||
Sponsor Name:University College London | |||||||||||||
Full Title: Phase II Study of Reduced Intensity Sibling Allogeneic Transplantation for Relapsed, Chemosensitive, PET Positive Hodgkin Lymphoma. Key words: Reduced intensity conditioning, Transplantation, Hodg... | |||||||||||||
Medical condition: Relapsed Hodgkin Lymphoma | |||||||||||||
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Population Age: Adolescents, Under 18, Adults | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2005-000279-16 | Sponsor Protocol Number: TRALG 1/02 | Start Date*: 2007-06-07 |
Sponsor Name:Sahlgrenska University Hospital | ||
Full Title: Phase III Clinical Study of Allogeneic Stem Cell Transplantation with Reduced Conditioning (RICT) versus Best Standard of Care in Acute Myeloid Leukemia (AML) in First Complete Remission | ||
Medical condition: Acute myeloid leukemia in first complete remission | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: FI (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2019-003723-37 | Sponsor Protocol Number: INHIBIT2019 | Start Date*: 2020-01-08 |
Sponsor Name:Institut klinické a experimentální medicíny (IKEM) | ||
Full Title: rATG versus rATG combined with IVIG induction immunosuppression in HLA incompatible transplantation | ||
Medical condition: Trial participants will be end-stage renal disease (ESRD) patients listed for deceased donor / living donor kidney transplantation with anti HLA antibody screening performed within 12 months before... | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: CZ (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2021-000853-17 | Sponsor Protocol Number: DKMS-21-01 | Start Date*: 2021-11-11 |
Sponsor Name:DKMS Group gGmbH | ||
Full Title: Graft vs Host Disease Prophylaxis in unrelated donor transplantation: a randomized clinical trial comparing PTCY vs ATG | ||
Medical condition: AML, t-MN, MDS, MDS/MPN, CMML-1/CMML-2 | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: DE (Ongoing) | ||
Trial results: (No results available) |
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