- Trials with a EudraCT protocol (246)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
246 result(s) found for: Hematopoietic stem cells.
Displaying page 1 of 13.
EudraCT Number: 2016-002383-13 | Sponsor Protocol Number: Cord_Blood_Expansion_(SR-1) | Start Date*: 2016-10-18 | |||||||||||
Sponsor Name:Erasmus MC | |||||||||||||
Full Title: Umbilical cord blood transplantation in high-risk hematological patients using stemregenin-1 expanded hematopoietic stem cells. A feasibility study focussing on engraftment and hematopoietic recov... | |||||||||||||
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) | |||||||||||||
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: 2009-011817-26 | Sponsor Protocol Number: BHS-UCB2009 | Start Date*: 2010-10-21 |
Sponsor Name:UZ Brussel VUB | ||
Full Title: A pilot study to assess the feasibility of unrelated umbilical cord blood transplantation with coinfusion of third-party mesenchymal stem cells after myeloablative or nonmyeloablative conditioning ... | ||
Medical condition: Adult patients with hematological malignancies | ||
Disease: | ||
Population Age: Adolescents, Under 18, Adults | Gender: Male, Female | |
Trial protocol: BE (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2009-013798-16 | Sponsor Protocol Number: | Start Date*: 2010-02-01 | |||||||||||||||||||||||||||||||
Sponsor Name:Royal Liverpool and Broadgreen University Hospitals NHS Trust | |||||||||||||||||||||||||||||||||
Full Title: A comparison of plerixafor/G-CSF with chemotherapy/G-CSF for stem cell transplantation | |||||||||||||||||||||||||||||||||
Medical condition: Patients with lymphoma or myeloma, who require high dose chemotherapy with autologous stem cell rescue (known colloquially as an autograft). Plerixafor is used to mobilise the autologous stem cells... | |||||||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||||||||||||
Trial protocol: GB (Completed) | |||||||||||||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2021-006367-26 | Sponsor Protocol Number: IGTRegs | Start Date*: 2023-01-03 |
Sponsor Name:Πανεπιστήμιο Πατρών | ||
Full Title: Phase I / II study of HLA-G + induced T-regulatory cells (iG-Tregs) in patients after allogeneic hematopoietic stem cell transplantation from HLA compatible sibling / donor. | ||
Medical condition: Adopt immunotherapy in adult patients undergoing hematopoietic stem cell (HSCT) transplantation from a fully compatible donor sibling for the prevention and treatment of GvHD. | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GR (Trial now transitioned) | ||
Trial results: (No results available) |
EudraCT Number: 2013-003626-88 | Sponsor Protocol Number: HOO-MSC01 | Start Date*: 2014-01-17 |
Sponsor Name:Fakultní nemocnice Plzeň | ||
Full Title: The utilization of mesenchymal stem cells (MSC) for the treatment of graft versus host disease (GVHD) after allogeneic stem cell transplantation. | ||
Medical condition: The study is intended for patients after allogeneic hematopoietic stem cell transplantation (from related and unrelated donors) with steroid-refractory or steroid-dependent GVHD of any type: - Ste... | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: CZ (Completed) | ||
Trial results: View results |
EudraCT Number: 2006-004101-26 | Sponsor Protocol Number: TJB0601P1 | Start Date*: 2006-12-13 | |||||||||||
Sponsor Name:CHU Sart-Tilman | |||||||||||||
Full Title: Mesenchymal stem cell infusion as prevention for graft rejection and graft-versus-host disease after allogeneic hematopoietic cell transplantation with nonmyeloablative conditioning: a pilot study | |||||||||||||
Medical condition: Patients with hematological malignancies not candidate for conventional allogeneic transplantation because of age or comorbidities. | |||||||||||||
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Population Age: Infants and toddlers, Children, Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2012-001335-31 | Sponsor Protocol Number: virus-specific_CD8_T-cells_001 | Start Date*: 2013-11-08 |
Sponsor Name:Univerzita Karlova v Praze, 2. lékařská fakulta | ||
Full Title: Adoptive transfer of CMV specific CD8+ T-cells to treat CMV infection after transplantation | ||
Medical condition: chronic CMV infection after allogeneic hematopoietic stem cell transplantation in children, refractory to conventional antiviral treatment | ||
Disease: | ||
Population Age: Infants and toddlers, Children, Adolescents, Under 18 | Gender: Male, Female | |
Trial protocol: CZ (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2008-003185-26 | Sponsor Protocol Number: CIK 2 | Start Date*: 2009-04-14 | |||||||||||
Sponsor Name:AZIENDA OSPEDALIERA "OSPEDALI RIUNITI DI BERGAMO" (A.O. DI RILIEVO NAZIONALE) | |||||||||||||
Full Title: Sequential Infusion of Unmanipulated Donor Lymphocytes and Cytokine Induced Killer (CIK) cells after allogeneic stem cell transplantation | |||||||||||||
Medical condition: Patients with haematologic malignancies (excluding CML) | |||||||||||||
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Population Age: Children, Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2013-003403-19 | Sponsor Protocol Number: HCK1 | Start Date*: 2013-09-25 |
Sponsor Name:Karolinska University Hospital | ||
Full Title: Study of T- and B-cell immunity after vaccination with a virosomebased influenza vaccine (Inflexal V) in patients who have undergone hematopoietic allogeneic stem cell transplantation. | ||
Medical condition: Allogeneic stem cell transplantation | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: SE (Completed) | ||
Trial results: View results |
EudraCT Number: 2011-002434-40 | Sponsor Protocol Number: AST-MOMA | Start Date*: 2012-03-23 | |||||||||||
Sponsor Name:University Hospital Tuebingen | |||||||||||||
Full Title: Highdose Chemotherapy and transplantation of 34+ selected stem cell for progressive systemic sclerosis Modification according to manifestation | |||||||||||||
Medical condition: Systemic sclerosis | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2004-004545-18 | Sponsor Protocol Number: NA | Start Date*: 2005-04-26 |
Sponsor Name:CHU Sart Tilman | ||
Full Title: Cell therapy for cardiac repair through mobilization of hematopoietic stem cells and endothelial progenitors in patients with chronic ischemic cardiomyopathy. | ||
Medical condition: Chronic ischemic cardiac disease | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: BE (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2014-000659-10 | Sponsor Protocol Number: LMW-DS-103 | Start Date*: 2014-05-21 | |||||||||||
Sponsor Name:TikoMed AB | |||||||||||||
Full Title: A randomised, open-label, placebo-controlled, single centre study in healthy male volunteers to explore efficacy, safety and tolerability of single doses of low molecular weight dextran sulfate (LM... | |||||||||||||
Medical condition: Healthy volunteers (mobilization of haematopoietic stem cells) | |||||||||||||
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Population Age: Adults | Gender: Male | ||||||||||||
Trial protocol: SE (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2017-003523-30 | Sponsor Protocol Number: 38RC17.191 | Start Date*: 2017-12-18 | |||||||||||
Sponsor Name:University Hospital Grenoble | |||||||||||||
Full Title: Vaccination after hematopoietic stem cell transplantation : a randomized study estimating the interest of an additional injection for patients not reponding at M3. | |||||||||||||
Medical condition: Our aim is to determine whether an additional dose of inactivated vaccine can increase the rate of responders among patients who have not responded adequately after 3 injections | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2005-005913-40 | Sponsor Protocol Number: Treo TM | Start Date*: 2006-01-17 | |||||||||||
Sponsor Name:OSPEDALE POLICLINICO S. MATTEO | |||||||||||||
Full Title: A phase II, multicentre, clinical study evaluating the safety and efficacy of Treosulfan-based conditioning of allogenic transplantation of haemopoietic stem-cells in patients affected by Thalassem... | |||||||||||||
Medical condition: Thalassemia Major | |||||||||||||
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Population Age: Infants and toddlers, Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2016-004122-41 | Sponsor Protocol Number: 1 | Start Date*: 2017-04-10 |
Sponsor Name:Medical University Vienna, Dept. f. Transfusion Medicine | ||
Full Title: Plerixafor for stem cell mobilization in patients with multiple myeloma who mobilize moderate to optimize collection results - a randomized, placebo-controlled, double-blind study | ||
Medical condition: Stem cell mobilization with mozobil (plerixafor) in patients with multiple myeloma. | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: AT (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2005-000640-91 | Sponsor Protocol Number: CMA-RC-03 | Start Date*: 2005-06-10 |
Sponsor Name:Institut de Recerca Hospital Sta. Creu i St. Pau | ||
Full Title: Treatment for acute myeloid leukemia (AML) during its first complete remision with the monoclonal antibody Mylotarg ® (anti-CD33/calicheamicina) pre- and post- autologous transplant of hematopoieti... | ||
Medical condition: Acute myeloid leukemia (AML) during its first complete remision and with high relapse risk, pre- and post- autologous hematopoiteic transplant | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: ES (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2010-023436-16 | Sponsor Protocol Number: HOVON 107 | Start Date*: 2011-05-31 | |||||||||||||||||||||
Sponsor Name:HOVON Foundation | |||||||||||||||||||||||
Full Title: The feasibility and efficacy of subcutaneous and intravenous Plerixafor for mobilization of peripheral blood stem cells in allogeneic HLA–identical sibling donors: a randomized phase II study. | |||||||||||||||||||||||
Medical condition: stem cell mobilization | |||||||||||||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: NL (Ongoing) DE (Restarted) | |||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2012-002879-34 | Sponsor Protocol Number: PSCT16 | Start Date*: 2013-03-05 |
Sponsor Name:Radboud University Nijmegen Medical Centre | ||
Full Title: Vaccination with minor histocompatibility antigen-loaded donor DC vaccines to boost graft-versus-tumor immunity after allogeneic stem cell transplantation | ||
Medical condition: Patients with aggressive hematological malignancies treated with allogeneic stem cell transplantation | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: NL (Completed) | ||
Trial results: View results |
EudraCT Number: 2019-002343-14 | Sponsor Protocol Number: RAG1-2019-01 | Start Date*: 2020-09-25 |
Sponsor Name:Leiden University Medical Center | ||
Full Title: PHASE I/II CLINICAL TRIAL OF AUTOLOGOUS HEMATOPOIETIC STEM CELL GENE THERAPY FOR RAG1-DEFICIENT SEVERE COMBINED IMMUNODEFICIENCY | ||
Medical condition: Patients with severe combined immunodeficiency (SCID) based on a genetic defect in the Recombinase Activating Gene 1 (RAG1) | ||
Disease: | ||
Population Age: Infants and toddlers, Under 18 | Gender: Male, Female | |
Trial protocol: NL (Trial now transitioned) ES (Ongoing) PL (Trial now transitioned) IT (Trial now transitioned) | ||
Trial results: (No results available) |
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