- Trials with a EudraCT protocol (680)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
680 result(s) found for: Cellular.
Displaying page 2 of 34.
| EudraCT Number: 2019-002541-37 | Sponsor Protocol Number: O2019-1 | Start Date*: 2019-10-09 |
| Sponsor Name:Region Örebro län | ||
| Full Title: Primary TBE vaccination for the elderly | ||
| Medical condition: Immune response to TBE vaccination | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: SE (Ongoing) | ||
| Trial results: View results | ||
| EudraCT Number: 2014-000570-19 | Sponsor Protocol Number: TBE_obesity_1.1 | Start Date*: 2014-07-11 |
| Sponsor Name:Institute of Specific Prophylaxis and Tropical Medicine | ||
| Full Title: Applikation of FSME-IMMUN® in obese persons | ||
| Medical condition: Studies have shown that obesity has a direct effect on the immune system and leads to immunosuppression, which leads to a susceptibility to infection. The aim of this study is to clarify if a modif... | ||
| Disease: | ||
| Population Age: Adults | Gender: Male, Female | |
| Trial protocol: AT (Completed) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2008-006772-30 | Sponsor Protocol Number: 20-026 | Start Date*: 2009-03-10 | ||||||||||||||||
| Sponsor Name:Medical University of Graz | ||||||||||||||||||
| Full Title: Evaluation of HCV clearance by hemodialysis | ||||||||||||||||||
| Medical condition: Chronic hepatitis C in patients with chronic renal failure | ||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
| Trial protocol: AT (Completed) | ||||||||||||||||||
| Trial results: View results | ||||||||||||||||||
| EudraCT Number: 2022-003041-35 | Sponsor Protocol Number: TJB2224 | Start Date*: 2022-10-20 |
| Sponsor Name:CHU de Liège | ||
| Full Title: Impact of the immune system on response to inactivated influenza vaccine (IIV) in allogeneic stem cell recipients | ||
| Medical condition: Allogeneic hematopoietic stem cell recipients | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: BE (Completed) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2021-000300-38 | Sponsor Protocol Number: 001610 | Start Date*: 2021-02-05 |
| Sponsor Name:Antwerp University Hospital | ||
| Full Title: Vaccination against cOvid-19 In CancER patients under active treatment (Belgium, B-VOICE) | ||
| Medical condition: Onco-hematological patients | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: BE (Completed) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2017-004385-94 | Sponsor Protocol Number: CCTL019E2202 | Start Date*: 2018-07-30 | ||||||||||||||||
| Sponsor Name:Novartis Pharma AG | ||||||||||||||||||
| Full Title: A Phase II, single arm, multicenter open label trial to determine the efficacy and safety of tisagenlecleucel (CTL019) in adult patients with refractory or relapsed follicular lymphoma | ||||||||||||||||||
| Medical condition: Adult patients with refractory or relapsed follicular lymphoma | ||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
| Trial protocol: BE (Trial now transitioned) GB (GB - no longer in EU/EEA) AT (Completed) ES (Ongoing) DE (Trial now transitioned) FR (Trial now transitioned) NL (Trial now transitioned) IT (Trial now transitioned) | ||||||||||||||||||
| Trial results: (No results available) | ||||||||||||||||||
| EudraCT Number: 2016-002894-36 | Sponsor Protocol Number: IXIARO-booster-senescence | Start Date*: 2017-12-22 |
| Sponsor Name:Medical University of Vienna (MUW) | ||
| Full Title: "An open, monocentric, uncontrolled phase 4 trial to characterise cellular and humoral immune responses following the first booster immunisation with the inactivated, purified Japanese Encephalitis... | ||
| Medical condition: The condition under investigation is the naturally aging immune system. The aim of this study is to investigate the immune responses following a booster immunisation with the Japanese Encephalitis ... | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: AT (Completed) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2021-002363-22 | Sponsor Protocol Number: IIV-482 | Start Date*: 2021-05-27 |
| Sponsor Name:National Institute for Public Health and the Environment | ||
| Full Title: Vaccination of older persons against Sars-Cov-2 and cellular immunogenicity for long term protection (participating in the Doetinchem Cohort Study) | ||
| Medical condition: SARS-CoV-19, frailty | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: NL (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2004-004983-56 | Sponsor Protocol Number: 3010410 | Start Date*: 2005-02-28 |
| Sponsor Name:Hull and East Yorkshire Hospitals NHS Trust [...] | ||
| Full Title: A randomised placebo controlled trial of pre-operative statin use in elective abdominal aortic aneurysm repair to determine the effect on systemic and cellular responses of ischaemia reperfusion in... | ||
| Medical condition: Ischaemia reperfusion injury following elective abdominal aortic aneurysm repair. This occurs when muscle or organ is subjected to an ischaemic insult with associated damage followed by reperfusio... | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: GB (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2012-005450-30 | Sponsor Protocol Number: ABI-MS-P01 | Start Date*: 2014-01-08 |
| Sponsor Name:Medizinische Universität Innsbruck | ||
| Full Title: Anti-Biopharmaceutical Immunization: Prediction and analysis of clinical relevance to minimize the risk of immunization in multiple sclerosis patients on interferon-beta treatment | ||
| Medical condition: Development of neutralising antibodies against Interferon-beta in the treatment of multiple sclerosis | ||
| Disease: | ||
| Population Age: Adults | Gender: Male, Female | |
| Trial protocol: AT (Completed) SE (Ongoing) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2021-006754-31 | Sponsor Protocol Number: 80101 | Start Date*: 2022-03-22 |
| Sponsor Name:Leiden University Medical Center | ||
| Full Title: Establishing immunogenicity and safety of needle-free intradermal delivery by nanoporous ceramic skin patch of mRNA SARS-CoV-2 vaccine as a revaccination strategy in healthy volunteers | ||
| Medical condition: Safety and immunogenicity after revaccination with Spikevax in healthy adults who have received Comirnaty as a primary vaccine | ||
| Disease: | ||
| Population Age: Adults | Gender: Male, Female | |
| Trial protocol: NL (Ongoing) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2022-000905-29 | Sponsor Protocol Number: RENOIR | Start Date*: 2022-04-12 | |||||||||||
| Sponsor Name:ISTITUTO NAZIONALE PER LE MALATTIE INFETTIVE "LAZZARO SPALLANZANI" | |||||||||||||
| Full Title: Temporal kinetics of antibody and cellular response markers and relative impact of revaccination in patients recovered from COVID-19 after treatment with monoclonal antibodies | |||||||||||||
| Medical condition: Covid-19 infection | |||||||||||||
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| Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: IT (Trial now transitioned) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2017-002116-14 | Sponsor Protocol Number: CCTL019G2201J | Start Date*: 2018-10-22 | ||||||||||||||||
| Sponsor Name:Novartis Pharma AG | ||||||||||||||||||
| Full Title: A phase II trial of tisagenlecleucel in first-line high-risk (HR) pediatric and young adult patients with B-cell acute lymphoblastic leukemia (B-ALL) who are minimal residual disease (MRD) positive... | ||||||||||||||||||
| Medical condition: Pediatric and young adult patients aged 1 to 25 years with first-line NCI high-risk (HR) B-cell acute lymphoblastic leukemia (B-ALL) who are in CR1 with minimal residual disease (MRD) positive (MR... | ||||||||||||||||||
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| Population Age: Infants and toddlers, Children, Adolescents, Under 18, Adults | Gender: Male, Female | |||||||||||||||||
| Trial protocol: BE (Trial now transitioned) ES (Temporarily Halted) DK (Trial now transitioned) FR (Trial now transitioned) IT (Trial now transitioned) GB (GB - no longer in EU/EEA) DE (Completed) FI (Completed) NL (Trial now transitioned) NO (Trial now transitioned) SE (Trial now transitioned) | ||||||||||||||||||
| Trial results: (No results available) | ||||||||||||||||||
| EudraCT Number: 2013-003809-26 | Sponsor Protocol Number: SP010 | Start Date*: 2013-12-04 | |||||||||||
| Sponsor Name:SOTIO a.s. | |||||||||||||
| Full Title: Open-label, one-arm, multi-centre phase II clinical trial with second cycle of active cellular immunotherapy DCVAC/PCa in patients with localized prostate cancer after primary radical prostatectomy... | |||||||||||||
| Medical condition: Localized prostate cancer | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male | ||||||||||||
| Trial protocol: CZ (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2021-001512-28 | Sponsor Protocol Number: COVIM | Start Date*: 2021-05-11 | |||||||||||
| Sponsor Name:Charité - Universitätsmedizin Berlin | |||||||||||||
| Full Title: Immunogenicity of COVID-19 vaccines in medical staff and special risk populations | |||||||||||||
| Medical condition: SARS-CoV-2 immunogenicity | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DE (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2016-001718-31 | Sponsor Protocol Number: VAC063 | Start Date*: 2016-08-24 |
| Sponsor Name:University of Oxford, CTRG | ||
| Full Title: A Phase I/IIa clinical trial to assess the safety, immunogenicity and efficacy of the blood-stage Plasmodium falciparum malaria vaccine candidate RH5.1/AS01 | ||
| Medical condition: Plasmodium falciparum malaria | ||
| Disease: | ||
| Population Age: Adults | Gender: Male, Female | |
| Trial protocol: GB (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2011-000765-12 | Sponsor Protocol Number: MICORYX | Start Date*: 2011-08-22 | |||||||||||
| Sponsor Name:Oryx GmbH & Co. KG | |||||||||||||
| Full Title: Phase I/IIa study of immunization with frameshift peptides administered with Montanide ISA-51 VG in patients with advanced MSI-H colorectal cancer | |||||||||||||
| Medical condition: advanced MSI-H colorectal cancer | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DE (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2007-002104-18 | Sponsor Protocol Number: GID25 | Start Date*: 2007-08-27 |
| Sponsor Name:Sanofi Pasteur SA | ||
| Full Title: Evaluation of the Cellular, Humoral and Mucosal Immune Response in Adults and Elderly Subjects Vaccinated either with an Inactivated Influenza Vaccine Administered via the Intradermal Route or an I... | ||
| Medical condition: Vaccination of adult subjects aged 18 to 40 years and elderly subjects aged 60 to 85 years with an inactivated, split-virion influenza vaccine administered via the intradermal route using Vaxigrip®... | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: FR (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2015-001932-38 | Sponsor Protocol Number: FLU-v003 | Start Date*: 2016-07-22 | |||||||||||
| Sponsor Name:PepTcell Limited (trading as SEEK) | |||||||||||||
| Full Title: A randomised, double-blind, placebo-controlled, single-centre phase IIb trial as part of the EU-funded UNISEC project to assess the immunogenicity and safety of different formulations and dosing re... | |||||||||||||
| Medical condition: Influenza A and/or B | |||||||||||||
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| Population Age: Adults | Gender: Male, Female | ||||||||||||
| Trial protocol: NL (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2017-004610-26 | Sponsor Protocol Number: OVG2017/10 | Start Date*: 2018-11-28 | |||||||||||
| Sponsor Name:Clinical Trials and Research Governance (CTRG), University of Oxford | |||||||||||||
| Full Title: Evaluating the Long Term Immunogenicity of adenoviral and MVA vectored Ebola vaccine schedules and response to late boosting with AD26.ZEBOV vaccine: an open-label clinical trial | |||||||||||||
| Medical condition: Ebola Virus Disease | |||||||||||||
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| Population Age: Adults | Gender: Male, Female | ||||||||||||
| Trial protocol: GB (GB - no longer in EU/EEA) | |||||||||||||
| Trial results: View results | |||||||||||||
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