- Trials with a EudraCT protocol (356)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (4)
356 result(s) found for: Immunity.
Displaying page 1 of 18.
EudraCT Number: 2015-004406-42 | Sponsor Protocol Number: FCO-TIM-2015-01 | Start Date*: 2016-03-10 |
Sponsor Name:FIBICO | ||
Full Title: CLINICAL TRIAL TO ASSEES THE NON-INFERIORITY OF THE SUSPENSION OF PROPHYLACTIC TREATMENT WITH VALGANCICLOVIR IN KIDNEY TRANSPLANT CMV-seropositive PATIENTS, WHO MANTEIN CD8+ CMV- CELLULAR IMMUNI... | ||
Medical condition: Kidney transplant cytomegalovirus-seropositive | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: ES (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2019-004541-33 | Sponsor Protocol Number: immvzmpr1 | Start Date*: Information not available in EudraCT |
Sponsor Name:Västra Götalandsregionen | ||
Full Title: A clinical study to examine cellular and humoral immunity against measles and chickenpox in children and adolescents 0-18 years in childhood cancer. | ||
Medical condition: This study will be conducted as a longitudinal study. Former studies have shown that immunity is affected after treatment against childhood cancer. We want to investigate humoral and cell-mediated ... | ||
Disease: | ||
Population Age: Adolescents, Under 18 | Gender: Male, Female | |
Trial protocol: SE (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2020-002456-21 | Sponsor Protocol Number: 74082 | Start Date*: 2020-05-28 |
Sponsor Name:Radboudumc | ||
Full Title: Enhancing the BCG-induced trained immunity response by addition of bisphosphonate or MMR vaccine: a possible preventive approach against COVID-19 (BCG-PLUS) | ||
Medical condition: Trained immunity COVID-19 This study will investigate whether oral bisphosphonate supplementation or the MMR vaccine can be used as immune potentiators when simultaneously administered with BCG, t... | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: NL (Completed) | ||
Trial results: View results |
EudraCT Number: 2016-001901-18 | Sponsor Protocol Number: LGS.MMR.01.2016.2022 | Start Date*: 2017-02-14 | |||||||||||
Sponsor Name:The Danish National University Hospital "Rigshospitalet" | |||||||||||||
Full Title: Measles-mumps-rubella vaccine at 6 months of age, immunology, and childhood morbidity in a high-income setting | |||||||||||||
Medical condition: Infection with measles, mumps or rubella | |||||||||||||
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Population Age: Preterm newborn infants, Infants and toddlers, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2011-002928-41 | Sponsor Protocol Number: Immunity_TBE | Start Date*: 2013-01-14 |
Sponsor Name:Med. Uni. Wien, Klinik für Innere I | ||
Full Title: Characterization of humoral and cellular immunity for tick-borne encephalitis (TBE) vaccination in allogeneic blood and marrow graft recipients: a pilot study | ||
Medical condition: Characterization of humoral and cellular immunity for tick-borne encephalitis (TBE) vaccination in allogeneic blood and marrow graft recipients: a pilot study Study group consists of patients 11... | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: AT (Completed) | ||
Trial results: View results |
EudraCT Number: 2008-002378-37 | Sponsor Protocol Number: LIS/IMM138 | Start Date*: 2008-12-23 |
Sponsor Name:National Institute of Health and the Environment (RIVM) | ||
Full Title: The longitudinal kinetics of long term cellular memory immunity against Bordetella pertussis in Dutch 8-9 years old children after ACV booster vaccination. | ||
Medical condition: Whooping cough is a respiratory disease caused by Bordetella pertussis. Young infants are mostly at risk, but older children are the main source of infection. Since the incidence of whooping cough... | ||
Disease: | ||
Population Age: Children, Under 18 | Gender: Male, Female | |
Trial protocol: NL (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2010-022703-22 | Sponsor Protocol Number: MItrial | Start Date*: 2011-01-03 |
Sponsor Name:NKI-AVL | ||
Full Title: Local immunotherapy by the synergism of monobenzone and imiquimod cream (MI) for cutanous metastases in stage III-IV melanoma patients. | ||
Medical condition: patients with cutanous melanoma (stage III-IV) | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: NL (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2021-002088-23 | Sponsor Protocol Number: DemiVac2021 | Start Date*: 2021-05-05 |
Sponsor Name:Sciensano | ||
Full Title: Covid-19: Safety and Immunogenicity of a Reduced Dose of the BioNTech/Pfizer BNT162b2 Vaccine in a Healthy Population (REDU-VAC) | ||
Medical condition: Healthy persons from age 18 till age 56 | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: BE (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2015-004099-31 | Sponsor Protocol Number: 116811 | Start Date*: 2016-07-26 | |||||||||||
Sponsor Name:Glaxosmithkline Biologicals | |||||||||||||
Full Title: Long-term persistence of immunity to hepatitis B in adults vaccinated 20 to 30 years ago with Engerix™-B. | |||||||||||||
Medical condition: Healthy volunteers (immunisation against infection caused by all known subtypes of hepatitis B virus). | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2013-003303-18 | Sponsor Protocol Number: rl.01.2013 | Start Date*: Information not available in EudraCT |
Sponsor Name:Gedeon Richter Polska Sp. z o. o. | ||
Full Title: Clinical phase IV study assessing the efficacy and safety of the medicinal product Groprinosin in treatment of recurrent airway inflammation in children with impaired cellular immunity and diagnose... | ||
Medical condition: Recurrent airway inflammation in children with impaired cellular immunity. | ||
Disease: | ||
Population Age: Children, Under 18 | Gender: Male, Female | |
Trial protocol: PL (Prematurely Ended) | ||
Trial results: (No results available) |
EudraCT Number: 2012-004231-24 | Sponsor Protocol Number: TBEB13 | Start Date*: 2013-03-05 |
Sponsor Name:Department für Virologie, Medizinische Universität Wien | ||
Full Title: Long-term immunity after primary vaccination against tick-borne encephalitis in the elderly | ||
Medical condition: long-term B-cell immunity against tick-borne encephalitis (TBE) in healthy volunteers who have received 3-dose primary vaccination at an age between 18 and 31 years or older than 60 years. | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: AT (Completed) | ||
Trial results: View results |
EudraCT Number: 2007-000684-16 | Sponsor Protocol Number: 03MI10 | Start Date*: 2010-01-21 | |||||||||||
Sponsor Name:Great Ormond Street Hospital NHS Trust / University College London - Institute of Child Health | |||||||||||||
Full Title: Gene therapy for SCID-X1 using a self-inactivating (SIN) gammaretroviral vector. | |||||||||||||
Medical condition: X-Linked severe combined Immunodeficiency (SCID-X1) | |||||||||||||
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Population Age: Newborns, Infants and toddlers, Children, Adolescents, Under 18 | Gender: Male | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2020-001678-31 | Sponsor Protocol Number: APHP200462 | Start Date*: 2020-04-28 |
Sponsor Name:Assistance Publique Hopitaux de Paris | ||
Full Title: Randomized controlled trial evaluating the efficacy of vaccination with Bacillus Calmette and Guérin (BCG) in the Prevention of COVID-19 via the strengthening of innate immunity in Health Care Work... | ||
Medical condition: COVID 19 Health care workers (medical or non-medical) in French hospitals in direct contact with COVID-19 patients, including nurses, medical doctors and other personnel working in wards in charge... | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: FR (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2012-001709-26 | Sponsor Protocol Number: IMS012012 | Start Date*: 2012-06-28 | |||||||||||
Sponsor Name:Sevapharma,a.s. | |||||||||||||
Full Title: Randomized, double-blind, placebo-controlled clinical trial of Immodin immunological efficacy in healthy adult volunteers. | |||||||||||||
Medical condition: Immunological efficacy, in healthy volunteers | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: CZ (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2021-004419-14 | Sponsor Protocol Number: T125/2020 | Start Date*: 2021-10-18 |
Sponsor Name:Turku University Hospital | ||
Full Title: COVID-19 infections in hospital personnel | ||
Medical condition: COVID-19 | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: FI (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2021-004891-33 | Sponsor Protocol Number: T33/2021 | Start Date*: 2022-04-13 |
Sponsor Name:Turku University Hospital | ||
Full Title: COVID-19 vaccine induced immune response in patients with primary antibody deficiency | ||
Medical condition: COVID-19 | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: FI (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2010-020450-33 | Sponsor Protocol Number: IX-senesc2.0 | Start Date*: 2010-06-23 | |||||||||||
Sponsor Name:Institute of Specific Prophylaxis and Tropical Medicine | |||||||||||||
Full Title: Characterization of cellular and humoral immunity in the elderly upon vaccination with the purified inactivated Japanese Encephalitis Vaccine IXIARO® | |||||||||||||
Medical condition: The aim of this project is to investigate humoral and cellular immune responses before and after immunisation with the Japanese encephalitis vaccine IXIARO in subjects above 65 years of age in comp... | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: AT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2008-005800-24 | Sponsor Protocol Number: version1.0 | Start Date*: 2008-10-22 | |||||||||||
Sponsor Name:Medizinische Universität Wien, Institut für Spezifische Prophylaxe und Tropenmedizin | |||||||||||||
Full Title: Characterisation of humoral and cellular immunity of low- and high-responder after TBE vaccination | |||||||||||||
Medical condition: The aim of this project is to investigate the humoral and cellular immune responses of low-responders after TBE vaccination in order to find parameters regarding immunoregulation against TBE. It is... | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: AT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2007-004978-16 | Sponsor Protocol Number: V59P5E1 | Start Date*: 2007-12-07 |
Sponsor Name:Novartis Vaccines and Diagnostics S.r.l. | ||
Full Title: A Phase 2, Open-label, Controlled, Multi-center Study to Evaluate Meningococcal ACWY Antibody Response in Children Aged 40 and 60 Months who Have Previously Received Novartis MenACWY Conjugate Vacc... | ||
Medical condition: Novartis Meningococcal ACWY Conjugate Vaccine is intended for prevention of meningitidis and septicemia caused by Neisseria meningitidis serogroups A, C, W-135 and Y. | ||
Disease: | ||
Population Age: Infants and toddlers, Children, Under 18 | Gender: Male, Female | |
Trial protocol: GB (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 (Ongoing) | ||
Trial results: (No results available) |
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