- Trials with a EudraCT protocol (42)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
42 result(s) found for: Influenza-like illness.
Displaying page 1 of 3.
EudraCT Number: 2014-001863-11 | Sponsor Protocol Number: EWO-ISO-2014/1 | Start Date*: 2014-09-24 | |||||||||||
Sponsor Name:Ewopharma AG. | |||||||||||||
Full Title: A Phase 4, Randomised, Placebo-Controlled, Double-Blind, Multicenter Study to Evaluate Efficacy of Isoprinosine® in Comparison With Placebo in Subjects With Confirmed Acute Respiratory Viral Infect... | |||||||||||||
Medical condition: Acute Respiratory Viral Infections due to influenza A or B virus, RSV, adenovirus, or parainfluenza virus 1 or 3 | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: CZ (Completed) SK (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2017-001103-77 | Sponsor Protocol Number: FLU007INVICTUS | Start Date*: 2017-09-05 | ||||||||||||||||
Sponsor Name:Vaccitech Limited | ||||||||||||||||||
Full Title: A phase IIb study to determine the safety and efficacy of candidate INfluenza Vaccine MVA-NP+M1 in combination with licensed InaCTivated inflUenza vaccine in adultS aged 65 years and above | ||||||||||||||||||
Medical condition: Influenza | ||||||||||||||||||
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Population Age: Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: GB (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2010-022682-98 | Sponsor Protocol Number: NL33774.000.10 | Start Date*: 2010-10-14 |
Sponsor Name:Julius Center for Health Sciences and Primary Care, UMC Utrecht | ||
Full Title: Monitoring of influenza-like symptoms among elderly, an observational study | ||
Medical condition: influenza-like illness (ILI) lower respiratory tract infection (LRTI) | ||
Disease: | ||
Population Age: Elderly | Gender: Male, Female | |
Trial protocol: NL (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2014-004471-23 | Sponsor Protocol Number: CB/ALICE/0010 | Start Date*: 2015-08-12 | |||||||||||
Sponsor Name:University of Oxford | |||||||||||||
Full Title: Antivirals for influenza Like Illness? An rCt of Clinical and Cost effectiveness in primary CarE | |||||||||||||
Medical condition: Influenza-like illness | |||||||||||||
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Population Age: Infants and toddlers, Children, Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: HU (Completed) BE (Completed) IE (Completed) GB (Completed) SE (Completed) CZ (Completed) LT (Completed) DK (Completed) NL (Completed) PL (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2013-001051-12 | Sponsor Protocol Number: 11RM013 | Start Date*: Information not available in EudraCT | |||||||||||
Sponsor Name:Nottingham University Hospitals NHS Trust | |||||||||||||
Full Title: Early low dose steroids for adults admitted to hospital with influenza-like illness during a pandemic: a randomised placebo controlled trial | |||||||||||||
Medical condition: Influenza-like illness | |||||||||||||
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Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2021-000401-24 | Sponsor Protocol Number: B4062020000134 | Start Date*: 2021-02-10 |
Sponsor Name:Sciensano | ||
Full Title: Influence of Prior Infection With COVID-19 on Occurrence of Influenza-like Illness or Acute Respiratory Infection (PICOV) A Non-commercial multicentre academic prospective cohort study in nursing ... | ||
Medical condition: Healthy persons from age 18 till age 100 | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: BE (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2013-001869-16 | Sponsor Protocol Number: BRN-C-2013-02 | Start Date*: 2013-09-24 | |||||||||||
Sponsor Name:Boiron Laboratoires | |||||||||||||
Full Title: A randomised, multi-centre, parallel group, double-blind, placebo-controlled study to assess the efficacy and safety of Oscillococcinum® in the treatment of symptoms of Influenza-like illness (ILI) | |||||||||||||
Medical condition: Systemic and respiratory symptoms of Influenza-like-illness (ILI) | |||||||||||||
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Population Age: Adolescents, Under 18, Adults | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2015-001514-97 | Sponsor Protocol Number: 114541 | Start Date*: 2015-05-27 |
Sponsor Name:GlaxoSmithKline Biologicals | ||
Full Title: A Phase 3, observer blind, randomized, non-influenza vaccine comparator-controlled, multi-country and multi-centre study of the efficacy of GSK Biologicals’ quadrivalent, inactivated, split virion,... | ||
Medical condition: Healthy volunteers (Immunization against influenza in male and female subjects 3 to 8 years of age inclusive) | ||
Disease: | ||
Population Age: Children, Under 18 | Gender: Male, Female | |
Trial protocol: Outside EU/EEA | ||
Trial results: View results |
EudraCT Number: 2020-002972-11 | Sponsor Protocol Number: BRN-C-2019-02 | Start Date*: 2020-09-21 |
Sponsor Name:BOIRON | ||
Full Title: Efficacy of Oscillococcinum® in the treatment of Influenza-like-illness symptoms: a national, multicentre, randomized, controlled trial | ||
Medical condition: Influenza-like illness (ILI) symptoms | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: FR (Completed) BE (Completed) | ||
Trial results: View results |
EudraCT Number: 2011-005929-49 | Sponsor Protocol Number: VX11-787-101 | Start Date*: 2012-02-20 | |||||||||||
Sponsor Name:Vertex Pharmaceuticals Incorporated | |||||||||||||
Full Title: A Phase 2a, Randomized, Double Blind, Placebo Controlled Study to Investigate the Effects of VX 787 Administered to Adult Volunteers Experimentally Inoculated with Live Influenza Virus | |||||||||||||
Medical condition: Influenza A | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2012-001515-22 | Sponsor Protocol Number: S54226 | Start Date*: 2012-05-16 |
Sponsor Name:Katholieke Universiteit Leuven | ||
Full Title: Cytomegalovirus infection and the influenza vaccination response in older persons | ||
Medical condition: Humoral and cellular immune response after vaccination in older people | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: BE (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2013-002822-21 | Sponsor Protocol Number: ARCHIE001 | Start Date*: 2013-10-10 | |||||||||||
Sponsor Name:University of Oxford | |||||||||||||
Full Title: The early use of Antibiotics for at Risk CHildren with InfluEnza in primary care (ARCHIE): a double-blind randomised placebo-controlled trial | |||||||||||||
Medical condition: Influenza or influenza-like illness | |||||||||||||
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Population Age: Infants and toddlers, Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2018-000468-27 | Sponsor Protocol Number: BVX-010 | Start Date*: 2018-07-04 | |||||||||||
Sponsor Name:BiondVax Pharmaceuticals Ltd. | |||||||||||||
Full Title: A pivotal, multicentre, randomized, modified double-blind, placebo-controlled phase 3 trial to assess the safety and clinical efficacy of M-001, an influenza vaccine administered intramuscularly tw... | |||||||||||||
Medical condition: Flu vaccination | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: HU (Completed) PL (Completed) LV (Completed) BG (Completed) HR (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2015-003250-41 | Sponsor Protocol Number: 1 | Start Date*: 2015-09-15 | |||||||||||
Sponsor Name:Public Health England | |||||||||||||
Full Title: Protection induced by Live Attenuated Influenza Vaccine (LAIV or Fluenz Tetra) - applied epidemiological study | |||||||||||||
Medical condition: There is no medical condition associated with this trial. The trial involves vaccination of healthy children with a licensed product according to the SmPC. The vaccination is Fluenz Tetra, a live... | |||||||||||||
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Population Age: Children, Adolescents, Under 18, Adults | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2006-002839-24 | Sponsor Protocol Number: 108134 | Start Date*: 2006-08-18 |
Sponsor Name:GlaxoSmithKline Biologicals | ||
Full Title: A randomized, double-blind, placebo-controlled, multi-country and multi-center, phase IV study to demonstrate the efficacy of GSK Biologicals’ influenza vaccine (Fluarix™) administered intramuscula... | ||
Medical condition: Immunization against influenza in male and female subjects aged 18 to 64 years | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: CZ (Completed) FI (Completed) | ||
Trial results: View results |
EudraCT Number: 2006-003284-31 | Sponsor Protocol Number: NV20236 | Start Date*: 2006-12-18 | |||||||||||
Sponsor Name:F.Hoffmann-La Roche Ltd. | |||||||||||||
Full Title: An open label multi-center trial of oseltamivir for the seasonal prophylaxis of influenza in children | |||||||||||||
Medical condition: Seasonal prophylaxis of influenza in immunocompromised subjects | |||||||||||||
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Population Age: Infants and toddlers, Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Prematurely Ended) DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2006-002468-24 | Sponsor Protocol Number: NV20234 | Start Date*: 2008-02-13 | |||||||||||
Sponsor Name:F.Hoffmann-La Roche Ltd. | |||||||||||||
Full Title: A double-blind, randomized, stratified, multi-center trial evaluating conventional and high dose oseltamivir in the treatment of immunocompromised patients with influenza | |||||||||||||
Medical condition: To investigate the optimal therapy for influenza in immunocompromised transplant recipients. | |||||||||||||
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Population Age: Infants and toddlers, Children, Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) ES (Completed) FR (Completed) BE (Completed) HU (Completed) LT (Completed) CZ (Completed) EE (Completed) IT (Completed) GR (Prematurely Ended) BG (Completed) LV (Completed) DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2016-001008-49 | Sponsor Protocol Number: NV22155 | Start Date*: 2016-09-30 | |||||||||||
Sponsor Name:F. Hoffmann-La Roche AG | |||||||||||||
Full Title: A randomized, multicenter trial of oseltamivir doses of 75 mg for 5 or 10 days versus 150 mg for 5 or 10 days in influenza patients with pandemic (H1N1) 2009 | |||||||||||||
Medical condition: Influenza | |||||||||||||
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Population Age: Infants and toddlers, Children, Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: Outside EU/EEA | |||||||||||||
Trial results: View results |
EudraCT Number: 2018-004015-49 | Sponsor Protocol Number: FLU010 | Start Date*: 2019-03-14 | |||||||||||
Sponsor Name:Vaccitech Ltd | |||||||||||||
Full Title: Efficacy of MVA-NP+M1 in the influenza H3N2 Human Challenge model | |||||||||||||
Medical condition: influenza disease | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2006-006263-23 | Sponsor Protocol Number: ML20910 | Start Date*: 2006-12-05 | |||||||||||
Sponsor Name:ROCHE | |||||||||||||
Full Title: Efficacy of Oseltamivir treatment in laboratory- confirmed influenza: evaluation of effect on viral shedding and on serum and cytoplasmatic inflammatory cytokine concentration. | |||||||||||||
Medical condition: Influenza type A and B virus infection | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Prematurely Ended) | |||||||||||||
Trial results: View results |
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