- Trials with a EudraCT protocol (55)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
55 result(s) found for: Cell mediated immunity.
Displaying page 1 of 3.
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 (Prematurely Ended) | ||
Trial results: (No results available) |
EudraCT Number: 2012-004240-30 | Sponsor Protocol Number: AIT-MULTIVIR-01 | Start Date*: 2014-06-18 | |||||||||||
Sponsor Name:Universitätsklinikum Erlangen | |||||||||||||
Full Title: Prospective, open-label, randomised, two-arm, controlled, multicentre clinical trial, phase I/IIa, for the evaluation of safety and efficacy of an adoptive immunotherapy with allogeneic CMV-/EBV-sp... | |||||||||||||
Medical condition: Immune deficiency after allogeneic stem cell transplantation | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Prematurely Ended) | |||||||||||||
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: 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: 2017-001819-36 | Sponsor Protocol Number: Sci-B-Vac–001 | Start Date*: 2018-02-02 | |||||||||||
Sponsor Name:VBI Vaccines Inc. | |||||||||||||
Full Title: A Phase 3 Double-Blind Randomized Controlled Trial to Compare the Immunogenicity and Safety of a Three-dose Regimen of Sci-B-Vac™ to a Three-dose Regimen of Engerix-B® in Adults (PROTECT) | |||||||||||||
Medical condition: Hepatitis B vaccination in healthy adults | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FI (Completed) BE (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: 2009-011152-22 | Sponsor Protocol Number: GTG003.08 | Start Date*: Information not available in EudraCT |
Sponsor Name:GENETHON | ||
Full Title: Phase 1/2 clinical trial of haematopoietic stem cell gene therapy for the Wiskott-Aldrich Syndrome | ||
Medical condition: Phase 1/2 clinical trial of haematopoietic stem cell gene therapy for the Wiskott-Aldrich Syndrome. An open labelled, non-randomised, phase I/II, cohort study involving a single infusion of autolo... | ||
Disease: | ||
Population Age: Children, Adolescents, Under 18 | Gender: Male | |
Trial protocol: FR (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: 2010-023791-63 | Sponsor Protocol Number: V70_34 | Start Date*: 2011-03-24 | |||||||||||
Sponsor Name:Novartis Vaccines and Diagnostics S.r.l. | |||||||||||||
Full Title: A Phase II, Randomized, Controlled, Observer-Blind, Clinical Study to Evaluate the Humoral and Cell Mediated Immunity and Safety of Two Intramuscular Doses of Fluad® or Agrippal® in Previously Unva... | |||||||||||||
Medical condition: influenza | |||||||||||||
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Population Age: Infants and toddlers, Children, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) BE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2019-001815-21 | Sponsor Protocol Number: 212340 | Start Date*: 2019-10-23 |
Sponsor Name:GlaxoSmithKline Biologicals | ||
Full Title: A phase IIIB, open label, long term follow-up study to assess persistence of immune responses to GSK’s HZ/su vaccine 4-7 years after primary vaccination; and immunogenicity and safety assessment of... | ||
Medical condition: Herpes Zoster | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: BE (Completed) FI (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2009-017141-58 | Sponsor Protocol Number: V111_06TP_OPERA | Start Date*: 2009-11-19 | |||||||||||
Sponsor Name:OPERA SRL | |||||||||||||
Full Title: An Open-Label Exploratory Clinical Study to Evaluate the Antibody and Cell Mediated Immunity of One Intramuscular Dose of MF59-Adjuvanted Egg-Derived, Inactivated Novel Swine Origin A/H1N1 Monovale... | |||||||||||||
Medical condition: Prophylaxis of A/H1N1sw influenza | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2015-000592-27 | Sponsor Protocol Number: 13102014 | Start Date*: 2015-06-18 |
Sponsor Name:Helsinki University Central Hospital | ||
Full Title: Immunodeficiency in cartilage-hair hypoplasia: sub-project on safety of vaccination against chickenpox | ||
Medical condition: Cartilage-hair hypoplasia patients. | ||
Disease: | ||
Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | |
Trial protocol: FI (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2019-003261-18 | Sponsor Protocol Number: VITAL | Start Date*: 2019-11-22 |
Sponsor Name: | ||
Full Title: The effects of allergen immunotherapy on anti-viral immunity in patients with allergic asthma | ||
Medical condition: Allergic asthma | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: DK (Completed) | ||
Trial results: View results |
EudraCT Number: 2007-002712-25 | Sponsor Protocol Number: V101P1 | Start Date*: 2007-10-29 |
Sponsor Name:Novartis Vaccines and Diagnostics GmbH & Co. KG | ||
Full Title: A Phase II, Randomized, Placebo-controlled, Observer-blind, Multi Center Study on the Safety and Immunogenicity of Novartis Tetravalent Influenza Vaccine (containing both interpandemic strains and ... | ||
Medical condition: Avian Influenza | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: DE (Completed) | ||
Trial results: View results |
EudraCT Number: 2013-004726-28 | Sponsor Protocol Number: ILIT2Linköping-Jönköping | Start Date*: 2014-01-10 |
Sponsor Name:Allergy Centre | ||
Full Title: Double-blind randomised controlled study to down regulate allergic responses in adults with allergic rhinoconjunctivitis by using three intralymphatic injections of grass and/or birch allergen one ... | ||
Medical condition: Allergic rhinoconjunctivitis | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: SE (Prematurely Ended) | ||
Trial results: (No results available) |
EudraCT Number: 2006-005203-33 | Sponsor Protocol Number: V87P3 | Start Date*: 2006-11-16 |
Sponsor Name:Novartis Vaccines and Diagnostics GmbH & Co. KG | ||
Full Title: A Phase II, Multicenter, Exploratory Study to Evaluate Safety and Immunogenicity of Two Doses of FLUAD-H5N1 Influenza Vaccine in Adults Unprimed and Primed with MF59-adjuvanted or Non-adjuvanted H5... | ||
Medical condition: avian influenza | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: GB (Completed) | ||
Trial results: View results |
EudraCT Number: 2016-003369-24 | Sponsor Protocol Number: ILIT-3L | Start Date*: 2017-01-03 |
Sponsor Name:Allergy Centre | ||
Full Title: Double-blind randomised controlled study to down regulate allergic responses in adults with allergic rhinoconjunctivitis by using three intralymphatic injections of grass and birch allergen or plac... | ||
Medical condition: Allergic rhinoconjunctivitis | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: SE (Prematurely Ended) | ||
Trial results: (No results available) |
EudraCT Number: 2021-006495-16 | Sponsor Protocol Number: PrEPSo | Start Date*: 2022-02-25 | |||||||||||
Sponsor Name:ISTITUTO NAZIONALE PER LE MALATTIE INFETTIVE "LAZZARO SPALLANZANI" | |||||||||||||
Full Title: Immunogenicity and safety of Sotrovimab (Vir 7831) IV as primary prophylaxis in anti-SARS-CoV-2 vaccine non responders | |||||||||||||
Medical condition: Covid 19 Infection | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2011-001943-60 | Sponsor Protocol Number: SJF0001 | Start Date*: 2011-06-20 | ||||||||||||||||
Sponsor Name:Lars Jørgen Østergaard | ||||||||||||||||||
Full Title: Cellular immunity in adult Hepatitis B-vaccinated serologic non-responders | ||||||||||||||||||
Medical condition: Healthy individuals | ||||||||||||||||||
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Population Age: Adults | Gender: Male, Female | |||||||||||||||||
Trial protocol: DK (Completed) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2020-001228-32 | Sponsor Protocol Number: COV002 | Start Date*: 2020-05-04 | |||||||||||
Sponsor Name:CTRG | |||||||||||||
Full Title: A phase 2/3 study to determine the efficacy, safety and immunogenicity of the candidate Coronavirus Disease (COVID-19) vaccine ChAdOx1 nCoV-19 | |||||||||||||
Medical condition: SARS-CoV-2 | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) | |||||||||||||
Trial results: (No results available) |
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