- Trials with a EudraCT protocol (366)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
366 result(s) found for: Vaccine therapy.
Displaying page 7 of 19.
EudraCT Number: 2017-000109-19 | Sponsor Protocol Number: V502-001 | Start Date*: 2017-01-27 | |||||||||||
Sponsor Name:Merck & Co., Inc. | |||||||||||||
Full Title: A Randomized, International, Double-Blinded (With In-House Blinding), Controlled With GARDASIL™, Dose-Ranging Study of Octavalent Human Papillomavirus (HPV) (Types 6, 11, 16, 18, 31, 45, 52, and 58... | |||||||||||||
Medical condition: vaccination against HPV infection/related disease | |||||||||||||
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Population Age: Adolescents, Under 18, Adults | Gender: Female | ||||||||||||
Trial protocol: Outside EU/EEA | |||||||||||||
Trial results: View results |
EudraCT Number: 2019-000793-27 | Sponsor Protocol Number: IRST100.42 | Start Date*: 2019-10-23 | |||||||||||||||||||||
Sponsor Name:ISTITUTO SCIENTIFICO ROMAGNOLO PER LO STUDIO E LA CURA DEI TUMORI (IRST) S.R.L. IRCCS | |||||||||||||||||||||||
Full Title: A phase II study on adjuvant Vaccination with dendritic cells loaded with autologous tumor homogenate in resected stage IV rare cancers: Head&Neck (H&N), neuroendocrine Tumors (NET) and soft tissue... | |||||||||||||||||||||||
Medical condition: Resected stage IV rare cancers: Head&Neck (H&N), neuroendocrine tumors (NET) and soft tissue sarcoma (STS). | |||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: IT (Trial now transitioned) | |||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2019-001868-30 | Sponsor Protocol Number: LP0160-1396 | Start Date*: 2020-08-04 | |||||||||||
Sponsor Name:LEO Pharma A/S | |||||||||||||
Full Title: A phase 3, randomised, double-blind, multi-centre trial to evaluate the efficacy, safety, and tolerability of brodalumab treatment compared to placebo (blinded) and ustekinumab (open-label) in adol... | |||||||||||||
Medical condition: Moderate-to-severe plaque psoriasis in adolescents from 12 to 17 years of age | |||||||||||||
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Population Age: Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Completed) DE (Prematurely Ended) GB (GB - no longer in EU/EEA) NL (Completed) BE (Completed) IT (Prematurely Ended) HU (Prematurely Ended) PL (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2006-006962-41 | Sponsor Protocol Number: CSTI571ADE60 | Start Date*: 2008-03-27 |
Sponsor Name:Charité Universitätsmedizin Berlin | ||
Full Title: Dendritic cells as autologous vaccine in patients with chronic myeloid leukemia | ||
Medical condition: Chronic myeloid leukemia is a malignant disease of the blood. Without therapy it has an unfavourable prognosis. Under first-line therapy with newer inhibitors of the thymidinkinase some few patien... | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: DE (Prematurely Ended) | ||
Trial results: View results |
EudraCT Number: 2013-004489-32 | Sponsor Protocol Number: CV-9104-007 | Start Date*: 2014-03-05 | |||||||||||
Sponsor Name:CureVac AG | |||||||||||||
Full Title: An open label Randomised Phase II Trial of RNActive® Cancer Vaccine (CV9104) in high risk and intermediate risk patients with prostate cancer | |||||||||||||
Medical condition: prostate carcinoma (intermediate and high risk) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male | ||||||||||||
Trial protocol: DE (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2017-003081-27 | Sponsor Protocol Number: EHVAT01/ANRSVRI05 | Start Date*: 2018-02-19 | |||||||||||
Sponsor Name:Inserm-ANRS | |||||||||||||
Full Title: EHVA T01(European HIV Vaccine Alliance Therapeutic Trial 01)/ANRS VRI05: A Phase I/II randomised therapeutic HIV vaccine trial in individuals who started antiretrovirals during primary or chronic i... | |||||||||||||
Medical condition: Human Immunodeficiency Virus (HIV) infection | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Prematurely Ended) FR (Prematurely Ended) ES (Prematurely Ended) IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2010-021356-26 | Sponsor Protocol Number: 111679 | Start Date*: 2011-01-03 | |||||||||||
Sponsor Name:GlaxoSmithKline Biologicals | |||||||||||||
Full Title: A Phase IIb, randomized, observer-blind, placebo controlled, multicenter primary/booster therapeutic vaccination study to determine efficacy and safety of F4co/ AS01B vaccine, administered intramus... | |||||||||||||
Medical condition: ART-naïve HIV-infected adults (ART: anti-retroviral therapy) | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) ES (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2011-001643-79 | Sponsor Protocol Number: SAS115358 | Start Date*: 2012-01-24 | |||||||||||
Sponsor Name:GlaxoSmithKline Research & Development Limited | |||||||||||||
Full Title: A 6-month safety and benefit study of inhaled fluticasone propionate/ salmeterol combination versus inhaled fluticasone propionate in the treatment of 6,200 pediatric subjects 4-11 years old with p... | |||||||||||||
Medical condition: Asthma | |||||||||||||
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Population Age: Children, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: HU (Completed) GB (Completed) LV (Completed) CZ (Completed) LT (Completed) ES (Completed) AT (Completed) SE (Not Authorised) BE (Completed) DK (Completed) NL (Completed) BG (Completed) IT (Completed) FI (Prematurely Ended) SK (Completed) DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2016-002724-83 | Sponsor Protocol Number: iHIVARNA-01 | Start Date*: 2017-02-22 | |||||||||||
Sponsor Name:Erasmus MC | |||||||||||||
Full Title: A phase IIa randomized, placebo controlled, double blinded study to evaluate the safety and immunogenicity of iHIVARNA-01 in chronically HIV-infected patients under stable combined antiretroviral t... | |||||||||||||
Medical condition: Chronic HIV-1 infection | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Completed) ES (Prematurely Ended) NL (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2021-003567-10 | Sponsor Protocol Number: 217023 | Start Date*: 2021-12-23 | |||||||||||
Sponsor Name:GLAXOSMITHKLINE BIOLOGICALS | |||||||||||||
Full Title: A phase 2, single-blinded, randomised, controlled multi-country study to evaluate the safety, reactogenicity, efficacy and immune response following sequential treatment with an anti-sense oligonuc... | |||||||||||||
Medical condition: Hepatitis B virus (HBV) infection | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Trial now transitioned) BE (Trial now transitioned) FR (Trial now transitioned) DE (Trial now transitioned) ES (Ongoing) RO (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2016-000121-40 | Sponsor Protocol Number: CNTO1275PSO3013 | Start Date*: 2016-05-02 | |||||||||||
Sponsor Name:Janssen-Cilag International N.V. | |||||||||||||
Full Title: A Phase 3 Open-label Study to Assess the Efficacy, Safety, and Pharmacokinetics of Subcutaneously Administered Ustekinumab in the Treatment of Moderate to Severe Chronic Plaque Psoriasis in Pedia... | |||||||||||||
Medical condition: Moderate to Severe Chronic Plaque Psoriasis | |||||||||||||
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Population Age: Children, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Completed) HU (Completed) DE (Completed) PL (Completed) FR (Completed) NL (Completed) Outside EU/EEA | |||||||||||||
Trial results: View results |
EudraCT Number: 2016-001557-41 | Sponsor Protocol Number: Adim-QIS-01 | Start Date*: 2016-09-09 | |||||||||||
Sponsor Name:Adimmune Corporation | |||||||||||||
Full Title: A Phase III, Multi-center, Single-dose, Randomized, Double-blind, Non-inferiority and Lot-to-lot Consistency Study of Immunogenicity and Safety Evaluation of AdimFlu-S Quadrivalent Inactivated Infl... | |||||||||||||
Medical condition: healthy volunteers | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2020-005915-39 | Sponsor Protocol Number: RT-CoV-2_01 | Start Date*: 2021-02-19 |
Sponsor Name:REITHERA SRL | ||
Full Title: COVID-19 A Phase II/III, Randomized, Stratified, Observer-Blind, Placebo-Controlled Study to Evaluate the Efficacy, Safety, and Immunogenicity of GRAd-COV2 Vaccine in Adults Aged 18 Years and Older | ||
Medical condition: Subjects exposed to SARS-COV-2 risk of infectious | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: IT (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2007-007200-16 | Sponsor Protocol Number: ISS T-002 | Start Date*: 2008-06-13 | |||||||||||
Sponsor Name:ISTITUTO SUPERIORE DI SANITA' | |||||||||||||
Full Title: A Phase II randomized, open label, immunogenicity and safety trial of the vaccine based on the recombinant biologically active HIV-1 Tat protein in anti-Tat negative HIV-1 infected HAART-treated ad... | |||||||||||||
Medical condition: HIV-1 infected subjects | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2019-001986-34 | Sponsor Protocol Number: T151/2019 | Start Date*: 2019-11-19 | |||||||||||
Sponsor Name:Turku University Hospital | |||||||||||||
Full Title: Exploring the impact of pertussis immunization during pregnancy on the differences in immune response of infants after primary immunization with an acellular pertussis containing vaccine: an open l... | |||||||||||||
Medical condition: Pertussis Infection | |||||||||||||
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Population Age: In utero, Newborns, Infants and toddlers, Children, Under 18, Adults | Gender: Male, Female | ||||||||||||
Trial protocol: FI (Completed) | |||||||||||||
Trial results: (No results available) |
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: 2007-002326-29 | Sponsor Protocol Number: 6115A1-3008 | Start Date*: 2007-10-11 | |||||||||||
Sponsor Name:Wyeth Research Division of Wyeth Pharmaceuticals Inc. | |||||||||||||
Full Title: A Phase 3, Randomized, Double-blind Trial to Evaluate the Safety, Tolerability, and Immunogenicity of a 13-Valent Pneumococcal Conjugate Vaccine When Administered Concomitantly With Trivalent Inact... | |||||||||||||
Medical condition: Pneumococcal infection | |||||||||||||
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Population Age: Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) BE (Completed) HU (Completed) NL (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2014-001299-79 | Sponsor Protocol Number: IMVX2014 | Start Date*: 2014-10-06 | |||||||||||
Sponsor Name:Department of Infectious Diseases, Odense University Hospital | |||||||||||||
Full Title: Pneumococcal vaccination of rheumatoid arthritis patients in immunomodulatory therapy | |||||||||||||
Medical condition: Immunoresponse on pneumococcal vaccination of rheumatoid arthritis patients in immunomodulatory therapy | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2011-000092-13 | Sponsor Protocol Number: INF-001 | Start Date*: 2011-05-16 |
Sponsor Name: | ||
Full Title: A trial aimed at enhancing immunity to Influenza in elderly individuals through reversal of immune senescence mediated by herpes virus infection. | ||
Medical condition: The trial is aimed to improve the efficiency of the seasonal influenza vaccine. Healthy volunteers who are positive for cytomegalovirus (CMV) will be recruited and given anti-viral treatment. We h... | ||
Disease: | ||
Population Age: Elderly | Gender: Male, Female | |
Trial protocol: GB (Completed) | ||
Trial results: View results |
EudraCT Number: 2014-004015-36 | Sponsor Protocol Number: IN-IT-236-1320 | Start Date*: 2015-02-16 |
Sponsor Name:AZIENDA OSPEDALIERA SAN PAOLO | ||
Full Title: Role of a switch strategy to elvitegravir, cobicistat, emtricitabine, tenofovir disoproxil fumarate (QUAD) on HIV reservoir and immune activation. | ||
Medical condition: Human Immunodeficiency Virus (HIV-1) Infection | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: IT (Completed) | ||
Trial results: (No results available) |
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