- Trials with a EudraCT protocol (1,149)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
1,149 result(s) found for: Plasma cells.
Displaying page 1 of 58.
EudraCT Number: 2014-005174-11 | Sponsor Protocol Number: U1111-1166-6923 | Start Date*: 2015-10-01 |
Sponsor Name:Uppsala University Hospital | ||
Full Title: A randomized, double-blinded placebo-controlled, paralleled designed, investigator sponsored study of the effect of the GLP-1 receptor agonist liraglutide on beta-cell function in C-peptide positiv... | ||
Medical condition: Beta-cell function in C-peptide positive type 1 diabetes | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: SE (Prematurely Ended) | ||
Trial results: View results |
EudraCT Number: 2023-000061-14 | Sponsor Protocol Number: BCN04-DASA | Start Date*: 2023-05-26 | |||||||||||
Sponsor Name:Institut de Recerca Germans Trias i Pujol | |||||||||||||
Full Title: Safety and Impact of Dasatinib on Viral Persistence and Inflammation in People with HIV under Antiretroviral Treatment | |||||||||||||
Medical condition: Human immunodeficiency virus (HIV) | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2011-004783-30 | Sponsor Protocol Number: ARD12858-MOZ23510 | Start Date*: 2013-01-21 | |||||||||||
Sponsor Name:Sanofi aventis recherche et développement | |||||||||||||
Full Title: A pilot, exploratory, randomized, phase 2 safety study evaluating tumor cell (plasma cell) mobilization and apheresis product contamination in plerixafor plus non-pegylated G-CSF mobilized patients... | |||||||||||||
Medical condition: Multiple Myeloma | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Completed) LT (Completed) SE (Completed) EE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2011-004651-40 | Sponsor Protocol Number: SNOXA12C301 | Start Date*: 2012-03-05 | |||||||||||
Sponsor Name:NOXXON Pharma AG | |||||||||||||
Full Title: A multi-center, open label, uncontrolled, Phase IIa clinical trial evaluating the safety and efficacy of NOX-A12 in combination with a background therapy of bortezomib and dexamethasone (VD) in pre... | |||||||||||||
Medical condition: Relapsed multiple myeloma | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) AT (Completed) IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2005-003599-39 | Sponsor Protocol Number: AMD3100-3102-DE | Start Date*: 2005-12-02 | |||||||||||
Sponsor Name:AnorMED Corp. | |||||||||||||
Full Title: A randomized, double-blind, placebo-controlled, comparative trial of AMD3100 (240 mcg/kg) plus G-CSF (10 mcg/kg) versus G-CSF (10 mcg/kg) plus placebo to mobilize and collect greater than or equal ... | |||||||||||||
Medical condition: Mobilization of stem cells prior to autologous stem cell transplantation in patients with multiple myeloma | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2012-004884-29 | Sponsor Protocol Number: 12-BI-505-02 | Start Date*: 2013-01-16 | |||||||||||
Sponsor Name:BioInvent International AB | |||||||||||||
Full Title: A single-arm, Open-label, Phase 2 Clinical Trial Evaluating Disease Response Following Treatment With BI-505, a Human Anti–Intercellular Adhesion Molecule 1 Monoclonal Antibody, In Patients With Sm... | |||||||||||||
Medical condition: Smoldering (asymptomatic) multiple myeloma | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: SE (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2008-005046-23 | Sponsor Protocol Number: POL 2 | Start Date*: 2009-03-23 | |||||||||||
Sponsor Name:Polyphor AG | |||||||||||||
Full Title: A Phase IIa, Proof of Concept Study to Determine the Degree of Mobilisation of CD34+ Cells Following Administration of POL6326 in Patients with Multiple Myeloma | |||||||||||||
Medical condition: Multiple Myeloma | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Restarted) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2017-002129-39 | Sponsor Protocol Number: XC.ROD.2017 | Start Date*: 2017-08-02 | |||||||||||
Sponsor Name:XCELL Medical Solutions | |||||||||||||
Full Title: Phase II Clinical Trial to Know the effectiviness and safety with a a treatment based in a therapy with serical autologous white cells versus the use of Platelet Rich Plasma in patients with rotu... | |||||||||||||
Medical condition: Patients with Rotulian Tendinopathy | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2010-023029-39 | Sponsor Protocol Number: Plerixafor-MM02 | Start Date*: 2012-02-21 | |||||||||||
Sponsor Name:AZIENDA OSPEDALIERA DI BOLOGNA POLICLINICO S. ORSOLA M. MALPIGHI | |||||||||||||
Full Title: Plerixafor MM02 - Plerixafor plus G-CSF after chemotherapy for the mobilization of Peripheral Blood Stem Cells (PBSCs) in Multiple Myeloma (MM) patients undergoing Autologous Stem Cell Transplanta... | |||||||||||||
Medical condition: multiple myeloma | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2008-004489-23 | Sponsor Protocol Number: NVI-248 | Start Date*: 2008-10-20 |
Sponsor Name:Netherlands Vaccine Institute | ||
Full Title: Development of cellular immune response after infant pneumococcal conjugate vaccinations | ||
Medical condition: Cellular immune response(long term memory) after following the infant immunisation programme with a pneumococcal conjugate vaccine (Prevenar). | ||
Disease: | ||
Population Age: Infants and toddlers, Children, Under 18 | Gender: Male, Female | |
Trial protocol: NL (Completed) | ||
Trial results: View results |
EudraCT Number: 2019-004604-35 | Sponsor Protocol Number: ICONMM | Start Date*: 2020-06-17 | |||||||||||
Sponsor Name:VU University Medical Center | |||||||||||||
Full Title: A phase 2 study of CC220 (iberdomide) combined with low-dose cyclophosphamide and dexamethasone in relapsed/refractory multiple myeloma (IberCd): ICON study | |||||||||||||
Medical condition: Relapsed/refractory multiple myeloma | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2021-000987-31 | Sponsor Protocol Number: 35RC17_8825_IMMUNO-MYELO | Start Date*: 2021-04-23 | |||||||||||
Sponsor Name:CHU Rennes | |||||||||||||
Full Title: Immunomonitoring and multiple myeloma: impact of lenalidomide on immune checkpoint expression | |||||||||||||
Medical condition: Multiple Myeloma | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2015-003862-10 | Sponsor Protocol Number: Dara-Atra | Start Date*: 2016-04-01 | |||||||||||
Sponsor Name:VU University Medical Center | |||||||||||||
Full Title: A phase 1 and phase 2 study of daratumumab in combination with all-trans retinoic acid in relapsed/refractory multiple myeloma | |||||||||||||
Medical condition: relapsed/refractory multiple myeloma | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2006-006480-23 | Sponsor Protocol Number: 10,176 | Start Date*: 2007-10-12 |
Sponsor Name:University Hospitals of Leicester | ||
Full Title: Autologous Bone Marrow-Derived Cells for Cardioprotection During Heart Surgery | ||
Medical condition: Improvement of cardioprotection during elective coronary artery bypass graft surgery using the patients own bone marrow cells. | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (Completed) | ||
Trial results: View results |
EudraCT Number: 2005-004885-18 | Sponsor Protocol Number: 1805/2004 | Start Date*: 2004-12-30 | |||||||||||
Sponsor Name:AZIENDA OSPEDALIERA PISANA | |||||||||||||
Full Title: Evaluation of febrile event during emopoietic progenitor cells aferesi post chemotherapy treatment in patients affected by multiple myeloma. | |||||||||||||
Medical condition: Multiple myeloma | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2007-005563-10 | Sponsor Protocol Number: TLI-001-2007 | Start Date*: 2007-11-30 | |||||||||||
Sponsor Name:FONDAZIONE NEOPLASIE SANGUE ONLUS | |||||||||||||
Full Title: Allogeneic Hematopoietic Cell Transplantation Using a Non-myeloablative Preparative Regimen of Total Lymphoid Irradiation and Anti-Thymocyte Globulin for Patients with Hematologic Malignancies | |||||||||||||
Medical condition: Preparative Regimen of Total Lymphoid Irradiation and Anti-Thymocyte Globulin for Patients with Hematologic Malignancies | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2014-005634-59 | Sponsor Protocol Number: TEA-001 | Start Date*: 2015-04-29 | |||||||||||
Sponsor Name:Aarhus University Hospital | |||||||||||||
Full Title: Toll-like receptor 9 enhancement of antiviral immunity in chronic HIV-1 infection: a phase 1b/2a trial (TEACH) | |||||||||||||
Medical condition: HIV | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2022-000358-26 | Sponsor Protocol Number: BETAF-RED | Start Date*: 2022-05-11 | |||||||||||
Sponsor Name:Institut d’Investigacions Biomèdiques August Pi i Sunyer | |||||||||||||
Full Title: Safety, tolerability, and efficacy of a dose reduction strategy based on bictegravir/emtricitabine/tenofovir alafenamide in virologically suppressed HIV-infected adults. | |||||||||||||
Medical condition: HIV infection | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2018-000813-19 | Sponsor Protocol Number: EURE-CART-1 | Start Date*: 2019-09-04 | ||||||||||||||||
Sponsor Name:MolMed S.p.A. | ||||||||||||||||||
Full Title: A Phase I-IIa trial to assess the safety and antitumor activity of autologous CD44v6 CAR T-cells in acute myeloid leukemia and multiple myeloma expressing CD44v6. | ||||||||||||||||||
Medical condition: Acute myeloid leukemia and Multiple myeloma | ||||||||||||||||||
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Population Age: Infants and toddlers, Children, Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: CZ (Prematurely Ended) IT (Prematurely Ended) | ||||||||||||||||||
Trial results: View results |
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) |
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