- Trials with a EudraCT protocol (101)
 - Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
 
		
	   		
	   		    
                    
                   	
                   	    101 result(s) found for: Autologous hematopoietic stem cell transplantation.
                    
                
			
   			
		
		Displaying page 1 of 6.
	
	
	| 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: 2014-003573-42 | Sponsor Protocol Number: 232100-0131 | Start Date*: 2014-11-11 | 
| Sponsor Name:Västra Götalandsregionen | ||
| Full Title: Antibody-mediated immune response after immunization with FSME-Immun(R) against Tick Borne Encephalitis(TBE) after hematopoietic autologous and allogeneic stem cell transplantation. | ||
| Medical condition: Patients have undergone allogeneic or autologous stem cell transplantation for hematological malignancies. | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: SE (Completed) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2005-003026-26 | Sponsor Protocol Number: ARL - GT 2005 | Start Date*: 2008-09-15 | |||||||||||
| Sponsor Name:University Medical Center Hamburg-Eppendorf | |||||||||||||
| Full Title: High-dose chemotherapy with transplantation of gene-modified haematopoietic stem cells for HIV-positive patients with malignant diseases indicating an HSCT | |||||||||||||
| Medical condition: HIV-positive patients with any malignant disease of the haematopoietic system indicating haematopoietic stem cell transplantation (autologous or allogeneic) | |||||||||||||
					
						
							
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| Population Age: Adults | Gender: Male, Female | ||||||||||||
| Trial protocol: DE (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| 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: 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: 2005-003337-40 | Sponsor Protocol Number: final version 2.0 | Start Date*: 2006-02-13 | 
| Sponsor Name:European Group for Blood and Marrow Transplantation (EMBT) | ||
| Full Title: Autologous Stem Cell Transplantation for Crohn's Disease ('ASTIC'-Trial: Autologous Stem Cell Transplantation International Crohn's Disease Trial) | ||
| Medical condition: Patients with Crohn's disease who have not responded to immunosupressant medication | ||
| Disease: | ||
| Population Age: Adults | Gender: Male, Female | |
| Trial protocol: GB (GB - no longer in EU/EEA) IT (Ongoing) BE (Completed) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2006-001269-40 | Sponsor Protocol Number: CT-1306 | Start Date*: 2008-10-29 | 
| Sponsor Name:Charité University Medicine | ||
| Full Title: Induction of Tolerance with Immunoablation and Autologous Hematopoietic Stem Cell Transplantation (ASCT) for Severe Systemic Lupus Erythematosus (SLE) Refractory to Standard Immunosuppressive Th... | ||
| Medical condition: Patients with systemic lupus erythematosus (SLE) will be under investigation who show high disease activity despite treatment with standard immunosuppressive therapies: high-dose corticosteroids an... | ||
| Disease: | ||
| Population Age: Adults | Gender: Male, Female | |
| Trial protocol: DE (Ongoing) | ||
| Trial results: View results | ||
| EudraCT Number: 2008-003537-25 | Sponsor Protocol Number: 04032008 | Start Date*: 2008-08-28 | 
| Sponsor Name:University Medical Center Groningen | ||
| Full Title: Can the steady-state hematopoiesis be improved post-ASCT by infusion of the autologous stem cell transplant directly in the bone marrow compartment. | ||
| Medical condition: Study population - patient age 18-65 years - eligible for an ASCT for lymphoma or MM - at least ≥ 10 x 106 CD34+ cells/kg have been collected during the previous performed leucofereses procedure | ||
| Disease: | ||
| Population Age: Adults | Gender: Male, Female | |
| Trial protocol: NL (Completed) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2021-001005-67 | Sponsor Protocol Number: AlloRelapseMMStudy | Start Date*: 2022-05-11 | |||||||||||
| Sponsor Name:University Medical Center Hamburg-Eppendorf | |||||||||||||
| Full Title: Allogeneic stem cell transplantation vs. conventional therapy as salvage therapy for relapsed / progressed patients with multiple myeloma after first-line therapy (AlloRelapseMMStudy) | |||||||||||||
| Medical condition: Multiple myeloma | |||||||||||||
					
						
							
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DE (Trial now transitioned) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2004-002944-90 | Sponsor Protocol Number: EORTC 65041 | Start Date*: 2005-07-26 | |||||||||||
| Sponsor Name:European Organisation for Research and Treatment of Cancer | |||||||||||||
| Full Title: A Multicenter, Open, Phase II Study to Estimate the activity and safety of Caspofungin (CASP) in the First-line Treatment of probable and proven Invasive Aspergillosis 'IA) in Patients with Hematol... | |||||||||||||
| Medical condition: Invasive aspergillosis in patients with haematological malignancies (HM)/autologous Hematopoietic Stem Cell Transplantation (HSCT) – group A- and patients with allogeneic HSCT transplantation – gro... | |||||||||||||
					
						
							
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DE (Completed) GB (Completed) BE (Completed) ES (Completed) IT (Completed) SK (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2018-001715-79 | Sponsor Protocol Number: BL-8040.SCM.301 | Start Date*: 2019-05-14 | |||||||||||
| Sponsor Name:BioLineRx Ltd. | |||||||||||||
| Full Title: A Phase III, Randomized, Double-Blinded, Placebo-Controlled, Multi-Centre Study Evaluating the Safety, Tolerability and Efficacy of Combination Treatment of BL-8040 and G-CSF as compared to Placebo... | |||||||||||||
| Medical condition: Hematopoietic Stem Cell mobilization in Multiple Myeloma | |||||||||||||
					
						
							
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: HU (Trial now transitioned) CZ (Prematurely Ended) ES (Ongoing) DE (Trial now transitioned) IT (Trial now transitioned) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2005-005210-20 | Sponsor Protocol Number: 2005-005210-20 | Start Date*: 2006-04-10 | 
| Sponsor Name:CHU Sart-Tilman | ||
| Full Title: Phase II trial of caspofungin as secondary prophylaxis for invasive fungal infections in patients with high-risk hematological malignancies undergoing intensive chemotherapy or hematopoietic stem ... | ||
| Medical condition: Acute leukemia during induction or consolidation therapy. Autologous HSCT for a hematological malignancy. Standard allogeneic HSCT with a myeloablative conditioning regimen. | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: BE (Completed) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2014-000130-37 | Sponsor Protocol Number: MM-SDX-105-01 | Start Date*: 2014-09-12 | 
| Sponsor Name:FONDAZIONE NEOPLASIE SANGUE ONLUS (FO.NE.SA. Onlus) | ||
| Full Title: Prospective, phase II study to evaluate the efficacy and the safety of a combination of bendamustine-melphalan as preparative regimen to autologous transplantation of hematopoietic cells for multi... | ||
| Medical condition: Multiple myeloma | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: IT (Completed) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2009-013856-61 | Sponsor Protocol Number: ReLApsE_RV-MM-GMMG-340 | Start Date*: 2010-07-14 | |||||||||||
| Sponsor Name:University Hospital Heidelberg | |||||||||||||
| Full Title: A phase III national, multicentre, randomized open-label study with Lenalidomide/Dexamethasone versus Lenalidomide/Dexamethasone and autologous stem cell transplantation followed by Lenalidomide m... | |||||||||||||
| Medical condition: Multiple Myeloma (1.-3. Progression/Relapse) | |||||||||||||
					
						
							
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DE (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2018-005046-10 | Sponsor Protocol Number: HEMSC42 | Start Date*: 2019-07-23 | ||||||||||||||||
| Sponsor Name:Radboud university medical center | ||||||||||||||||||
| Full Title: Anakinra: Efficacy of interleukin-1 pathway inhibitor anakinra for the management of fever during neutropenia and mucositis in patients with multiple myeloma receiving an autologous hematopoietic s... | ||||||||||||||||||
| Medical condition: Febrile neutropenia and mucositis | ||||||||||||||||||
					
						
							
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| Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
| Trial protocol: NL (Completed) | ||||||||||||||||||
| Trial results: (No results available) | ||||||||||||||||||
| EudraCT Number: 2021-000354-25 | Sponsor Protocol Number: 2.1 | Start Date*: 2021-11-11 | |||||||||||||||||||||
| Sponsor Name:FINBA | |||||||||||||||||||||||
| Full Title: A multicenter randomized trial of fosfomycin versus ciprofloxacin for febrile neutropenia in hematologic patients: efficacy and microbiologic safety. | |||||||||||||||||||||||
| Medical condition: Post-chemotherapy neutropenia with high risk of developing infection in patients with acute leukemia undergoing induction, autologous or allogeneic hematopoietic stem cell transplantation. | |||||||||||||||||||||||
					
						
							
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
| Trial protocol: ES (Ongoing) | |||||||||||||||||||||||
| Trial results: (No results available) | |||||||||||||||||||||||
| EudraCT Number: 2007-003657-87 | Sponsor Protocol Number: BCNHL | Start Date*: 2007-09-14 | |||||||||||
| Sponsor Name:ISTITUTO NAZIONALE PER LA CURA TUMORI | |||||||||||||
| Full Title: Reduced intensity conditioning with high-dose rituximab followed by allogeneic transplantation of hematopoietic cells for the treatment of relapsed/refractory B-cell non Hodgkins lymphomas | |||||||||||||
| Medical condition: B-cell non-Hodgkin lymphomas | |||||||||||||
					
						
							
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| Population Age: Adults | Gender: Male, Female | ||||||||||||
| Trial protocol: IT (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2008-001669-27 | Sponsor Protocol Number: CLLX2 | Start Date*: 2011-06-28 | |||||||||||
| Sponsor Name:Universitätsklinikum Heidelberg | |||||||||||||
| Full Title: A phase-III study on the value of allogeneic stem cell transplantation in poor-risk chronic lymphocytic leukemia by the German CLL Study Group (GCLLSG) and the German Cooperative Transplant Study G... | |||||||||||||
| Medical condition: High-risk and very high-risk chronic lymphocytic leukemia (CLL) | |||||||||||||
					
						
							
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| Population Age: Adults | Gender: Male, Female | ||||||||||||
| Trial protocol: DE (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2014-003572-23 | Sponsor Protocol Number: GCP#01.01.030 | Start Date*: 2017-12-27 | ||||||||||||||||
| Sponsor Name:Gamida Cell Ltd | ||||||||||||||||||
| Full Title: Allogeneic Stem Cell Transplantation of CordIn™, Umbilical Cord Blood-Derived Ex Vivo Expanded Stem and Progenitor Cells, in Patients with Hemoglobinopathies | ||||||||||||||||||
| Medical condition: Hemoglobinopathies | ||||||||||||||||||
					
						
							
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| Population Age: Children, Adolescents, Under 18, Adults | Gender: Male, Female | |||||||||||||||||
| Trial protocol: FR (Completed) | ||||||||||||||||||
| Trial results: View results | ||||||||||||||||||
| EudraCT Number: 2004-001117-34 | Sponsor Protocol Number: APL-B-013-02 | Start Date*: 2004-10-13 | 
| Sponsor Name:Pharma Mar S.A. | ||
| Full Title: A Phase II Multicenter,Open-Label, Clinical And Pharmacokinetic Study Of Aplidin® As A 1-Hour Weekly IV Infusion, In Patients With Relapsed Or Refractory aggressive non-Hodgkin’s Lymphoma. | ||
| Medical condition: Aggressive non-Hodgkin’s Lymphoma.For aggressive NHL patient cure is still the target of therapy and a CR is a prerequisite to achieve this goal. Salvage therapy needs more aggressive experimental ... | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: ES (Completed) IT (Completed) | ||
| Trial results: View results | ||
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