- Trials with a EudraCT protocol (732)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (11)
732 result(s) found for: Lymphocyte.
Displaying page 8 of 37.
EudraCT Number: 2017-001619-35 | Sponsor Protocol Number: P1200_41 | Start Date*: 2017-06-01 | |||||||||||
Sponsor Name:Cliniques Universitaires Saint-lus, Université catholique de Louvain | |||||||||||||
Full Title: Exploratory pathophysiological study in five patients suffering from new-onset lupus nephritis and treated with rituximab as first-line treatment | |||||||||||||
Medical condition: Lupus Nephritis | |||||||||||||
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Population Age: Adolescents, Under 18, Adults | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2020-001266-11 | Sponsor Protocol Number: BALMYS-19 | Start Date*: 2020-04-16 |
Sponsor Name:Fundación Instituto de Investigación Sanitaria Fundación Jiménez Diaz | ||
Full Title: Two-center, randomized, controlled clinical trial with two treatment arms to evaluate the safety and efficacy of intravenous administration of expanded allogeneic adipose tissue adult mesenchymal c... | ||
Medical condition: Respiratory distress secondary to SARS-Cov-2 infection | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: ES (Prematurely Ended) | ||
Trial results: (No results available) |
EudraCT Number: 2006-005007-34 | Sponsor Protocol Number: 2006-0101 | Start Date*: 2007-04-10 | |||||||||||
Sponsor Name:UMCU | |||||||||||||
Full Title: Bortezomib re-induction therapy combined with donor lymphocyte infusion in patients with relapsed Multiple Myeloma following allogeneic stem cell transplantation | |||||||||||||
Medical condition: multiple myeloma patients with relapse or progression of their disease after receiving an allogeneic stem cell transplantation | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2011-002656-14 | Sponsor Protocol Number: 1733 | Start Date*: 2012-06-11 |
Sponsor Name:Imperial College | ||
Full Title: A randomised, prospective study, assessing changes in cerebral function in treatment naive HIV-1 infected subjects commencing either boosted atazanavir with Truvada or boosted darunavir with maravi... | ||
Medical condition: HIV infection and cognitive function | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (Completed) | ||
Trial results: View results |
EudraCT Number: 2020-001160-28 | Sponsor Protocol Number: MedOPP376 | Start Date*: 2020-04-09 | |||||||||||
Sponsor Name:Medica Scientia Innovation Research S.L. (MEDSIR) | |||||||||||||
Full Title: A Randomized, Controlled, Open-Label, Phase II Trial to Evaluate the Efficacy and Safety of Tocilizumab Combined with Pembrolizumab (MK-3475) in Patients with Coronavirus Disease 2019 (COVID-19)-Pn... | |||||||||||||
Medical condition: Coronavirus Disease 2019 (COVID-19)-Pneumonia | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2010-021786-78 | Sponsor Protocol Number: V1_30.4.2010 | Start Date*: 2010-11-11 | |||||||||||
Sponsor Name:Medizinische Universität Wien | |||||||||||||
Full Title: Treatment of chronic lymphocytic leukemia with the use of an antiviral compound - a proof of principle study | |||||||||||||
Medical condition: Chronic lymphocytic leukemia | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: AT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2014-005093-11 | Sponsor Protocol Number: IVVAC-3S/P2 | Start Date*: 2015-01-14 | |||||||||||
Sponsor Name:InnaVirVax | |||||||||||||
Full Title: Multicentre, open-label, phase I/IIa clinical study of an immunoprotective therapeutic vaccine candidate (VAC-3S) in Human Immunodeficiency Virus type 1 (HIV-1) chronically infected patients virol... | |||||||||||||
Medical condition: Chronically infected HIV-1 patients under viral control on Anti-Retroviral therapy. | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2007-007587-21 | Sponsor Protocol Number: CLL10 | Start Date*: 2008-09-05 | |||||||||||
Sponsor Name:University of Cologne | |||||||||||||
Full Title: Phase III trial of combined immunochemotherapy with Fludarabine, Cyclophosphamide and Rituximab (FCR) versus Bendamustine and Rituximab (BR) in patients with previously untreated chronic lymphocyti... | |||||||||||||
Medical condition: patients (age 18 years or older) with chronic lymphocytic leukemia: Stage Binet C or stage Binet B and A requiring treatment | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) AT (Completed) DK (Completed) CZ (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2011-003201-14 | Sponsor Protocol Number: ERTUSO | Start Date*: 2012-03-02 | |||||||||||
Sponsor Name: Krankenhaus Nordwest GmbH | |||||||||||||
Full Title: Phase I/II, Open Label, Dose Escalating Study To Investigate Safety, Tolerability, And Preliminary Efficacy Of The Trifunctional Anti-HER-2/neu x Anti-CD3 Antibody Ertumaxomab In Patients With HER-... | |||||||||||||
Medical condition: Patients with HER2/neu (1+/SISH positive, 2+ and 3+) expressing solid tumors that are progressing after standard therapy | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2011-004822-85 | Sponsor Protocol Number: ABCSG-34 | Start Date*: 2012-01-05 |
Sponsor Name:ABCSG (Austrian Breast & Colorectal Cancer Study Group) | ||
Full Title: A prospective, open, randomized, phase-II study of a therapeutic cancer vaccine (L-BLP25, Stimuvax®) in the pre-operative treatment of women with primary breast cancer | ||
Medical condition: primary breast cancer | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Female | |
Trial protocol: AT (Completed) | ||
Trial results: View results |
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: 2015-001382-10 | Sponsor Protocol Number: CS/2015/4775 | Start Date*: 2019-01-21 | |||||||||||
Sponsor Name:University Hospitals Bristol NHS Foundation Trust | |||||||||||||
Full Title: Treatment of Barth Syndrome by CARDIOlipin MANipulation (CARDIOMAN): A randomised placebo controlled pilot trial conducted by the nationally commissioned Barth Syndrome Service | |||||||||||||
Medical condition: Barth Syndrome is a rare, life threatening, genetic disease which affects young males. It is caused by abnormal fats (lipids) in the powerhouses of cells (mitochondria) and those who suffer with it... | |||||||||||||
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Population Age: Children, Adolescents, Under 18, Adults | Gender: Male | ||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) | |||||||||||||
Trial results: View results |
EudraCT Number: 2021-001535-99 | Sponsor Protocol Number: CCTL019BUS03 | Start Date*: 2022-03-14 | |||||||||||
Sponsor Name:Novartis Pharmaceuticals Corporation | |||||||||||||
Full Title: A phase II, open label, multi-center trial to determine the efficacy and safety of tisagenlecleucel re-infusion in Pediatric and Adolescent Young Adult (AYA) patients with acute lymphoblastic leuke... | |||||||||||||
Medical condition: Paediatric patients with B-cell acute lymphoblastic leukaemia | |||||||||||||
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Population Age: Infants and toddlers, Children, Adolescents, Under 18, Adults | Gender: Male, Female | ||||||||||||
Trial protocol: Outside EU/EEA | |||||||||||||
Trial results: View results |
EudraCT Number: 2022-004112-28 | Sponsor Protocol Number: URO-EMDA-2022-1 | Start Date*: 2023-03-27 | |||||||||||
Sponsor Name:Guillem Abad Carratalà | |||||||||||||
Full Title: Randomized prospective study of the impact of preoperative instillation of mitomycin-C by electromotive drug administration (EMDA) in patients with non-muscle-infiltrating urothelial carcinoma | |||||||||||||
Medical condition: Non muscle invasive bladder tumor | |||||||||||||
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Population Age: Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Ongoing) | |||||||||||||
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) |
EudraCT Number: 2020-001321-31 | Sponsor Protocol Number: 24032020 | Start Date*: 2020-04-11 |
Sponsor Name:Hospital Universitario de Fuenlabrada | ||
Full Title: Prospective, phase II, randomized, open-label, parallel group study to evaluate the efficacy of hydroxychloroquine together with baricitinib, imatinib or early lopinavir / ritonavir in patients wit... | ||
Medical condition: Pneumonia due to SARS Cov2 (COVID-19) | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: ES (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2018-002476-40 | Sponsor Protocol Number: 17-APN-01 | Start Date*: 2019-05-07 | |||||||||||
Sponsor Name:CHU de Nice | |||||||||||||
Full Title: Personalized Medicine for Membranous Nephropathy PMMN | |||||||||||||
Medical condition: Idiopathic Membranous Nephropathy | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2019-002733-10 | Sponsor Protocol Number: Dual-Triple-ART | Start Date*: 2019-08-13 | |||||||||||
Sponsor Name:FUNDACIÓ LLUITA CONTRA LA SIDA | |||||||||||||
Full Title: Exploratory, open-label, randomized clinical trial to assess the efficacy of first-line dual vs. triple antiretroviral therapy (art) in hiv-1 reservoir and in peripheral compartments in hiv-infecte... | |||||||||||||
Medical condition: HIV infection | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2018-002886-21 | Sponsor Protocol Number: UC-0110/1809 | Start Date*: 2018-12-11 |
Sponsor Name:UNICANCER | ||
Full Title: A Phase III randomized study evaluating gemcitabine and paclitaxel versus gemcitabine alone after FOLFIRINOX failure or intolerance in Metastatic Pancreatic Ductal Adenocarcinoma. | ||
Medical condition: Metastatic Pancreatic Ductal Adenocarcinoma | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: FR (Completed) | ||
Trial results: View results |
EudraCT Number: 2016-001923-30 | Sponsor Protocol Number: TN-20 | Start Date*: 2016-09-26 | |||||||||||
Sponsor Name:TRIALNET COORDINATING CENTER AT THE UNIVERSITY OF SOUTH FLORIDA | |||||||||||||
Full Title: Exploring Immune Effects of Oral Insulin in Relatives at Risk for Type 1 Diabetes Mellitus | |||||||||||||
Medical condition: Type 1 Diabetes | |||||||||||||
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Population Age: Children, Adolescents, Under 18, Adults | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: (No results available) |
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