- Trials with a EudraCT protocol (61)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (6)
61 result(s) found for: Hemisphere.
Displaying page 1 of 4.
EudraCT Number: 2007-000752-14 | Sponsor Protocol Number: GRT82 | Start Date*: 2011-04-19 |
Sponsor Name:Sanofi Pasteur SA | ||
Full Title: Immunogenicity and Safety of the Inactivated, Split-Virion Influenza Vaccine, Northern Hemisphere 2007-2008 Formulation (Intramuscular Route) | ||
Medical condition: Vaccination of healthy subjects aged 18 to 60 years (i.e. to the day before the 61st birthday) or 61 years or above (from the day of the 61st birthday) on the day of inclusion with one dose of the ... | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (Completed) | ||
Trial results: View results |
EudraCT Number: 2006-000671-15 | Sponsor Protocol Number: GRT63 | Start Date*: 2006-05-04 |
Sponsor Name:Sanofi Pasteur SA | ||
Full Title: Immunogenicity and Safety of the Inactivated, Split-Virion Influenza Vaccine, Northern Hemisphere 2006-2007 Formulation (Intramuscular Route) | ||
Medical condition: Vaccination of healthy subjects aged 18 to 60 years (60 subjects) and over the 60 years (60 subjects) with one dose of the new formulation of the influenza vaccine for the 2006-2007 Northern Hemisp... | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (Completed) | ||
Trial results: View results |
EudraCT Number: 2008-000943-33 | Sponsor Protocol Number: GRT83 | Start Date*: 2008-04-23 |
Sponsor Name:Sanofi Pasteur SA | ||
Full Title: Immunogenicity and Safety of the Inactivated, Split-Virion Influenza Vaccine, Northern Hemisphere 2008-2009 Formulation (Intramuscular Route) | ||
Medical condition: Vaccination of healthy subjects aged 18 to 60 years (i.e. to the day before the 61st birthday) or 61 years or above (from the day of the 61st birthday) on the day of inclusion with one dose of the ... | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (Completed) | ||
Trial results: View results |
EudraCT Number: 2009-010761-22 | Sponsor Protocol Number: 82/09 | Start Date*: 2009-04-25 | |||||||||||
Sponsor Name:POLICLINICO UNIVERSITARIO AGOSTINO GEMELLI | |||||||||||||
Full Title: ECG changes and C-protein level variations during and after treatment with atorvastatin at different dosages in the secondary prevention of stroke. | |||||||||||||
Medical condition: Stroke | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2018-001279-19 | Sponsor Protocol Number: SONAS2018 | Start Date*: 2019-08-19 | |||||||||||
Sponsor Name:BURL Concepts, Inc. | |||||||||||||
Full Title: Evaluation of the SONAS® ultrasound device for the assessment of bilateral cerebral perfusion in subjects with acute stroke | |||||||||||||
Medical condition: Acute large vessel occlusion (LVO) stroke (NIHSS score: ≥ 10) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) AT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2013-000881-12 | Sponsor Protocol Number: M13-998 | Start Date*: 2013-07-11 | |||||||||||
Sponsor Name:Abbott Biologicals B.V | |||||||||||||
Full Title: Immunogenicity, Reactogenicity and Safety of the Trivalent Influenza Subunit Vaccine Influvac® for the Northern Hemisphere Season 2013/2014. An Open-Label, Baseline- Controlled Study in Two Age Gro... | |||||||||||||
Medical condition: Prophylaxis of Influenza | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) BE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2012-005243-25 | Sponsor Protocol Number: GID37 | Start Date*: 2013-04-16 | |||||||||||
Sponsor Name:Sanofi Pasteur | |||||||||||||
Full Title: Immunogenicity and Safety of the Trivalent Influenza Vaccine (Split-Virion, Inactivated), Northern Hemisphere 2013-2014 Formulation (Intradermal Route) | |||||||||||||
Medical condition: Prophylaxis of influenza (2013-2014 Northern Hemisphere Season) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2009-009977-85 | Sponsor Protocol Number: GID29 | Start Date*: 2009-05-19 |
Sponsor Name:Sanofi Pasteur SA | ||
Full Title: Immunogenicity and Safety of the Influenza Vaccine (Split Virion, Inactivated), Northern Hemisphere 2009-2010 Formulation (Intradermal Route) | ||
Medical condition: Vaccination of adults up to 59 years of age and elderly of 60 years of age and over with inactivated split-virion influenza vaccine administered by the intradermal route | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: FR (Completed) | ||
Trial results: View results |
EudraCT Number: 2014-000629-19 | Sponsor Protocol Number: GID47 | Start Date*: 2014-08-21 | |||||||||||
Sponsor Name:Sanofi Pasteur | |||||||||||||
Full Title: Safety assessment of the Trivalent Influenza Vaccine (Split-Virion, Inactivated), Northern Hemisphere 2014-2015 Formulation (Intradermal Route) | |||||||||||||
Medical condition: Prophylaxis of influenza (2014-2015 Northern Hemisphere Season) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2012-001032-57 | Sponsor Protocol Number: M13-567 | Start Date*: 2012-06-26 | |||||||||||
Sponsor Name:Abbott Biologicals B.V. | |||||||||||||
Full Title: Immunogenicity, Reactogenicity and Safety of the Trivalent Influenza Subunit Vaccine Influvac® for the Northern Hemisphere Season 2012/2013. An Open-Label, Baseline- Controlled Study in Two Age ... | |||||||||||||
Medical condition: Prophylaxis of Influenza | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) BE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2015-000175-27 | Sponsor Protocol Number: CSLCT-USF-10-69 | Start Date*: 2015-03-23 |
Sponsor Name:bioCSL Pty Ltd | ||
Full Title: A Phase IV, Multicenter, Randomized, Observer-blind, Parallel-arm Study to Evaluate the Safety and Tolerability of CSL’s Trivalent Influenza Virus Vaccine (CSL TIV) in Children 5 to Less Than 9 Yea... | ||
Medical condition: Influenza, human | ||
Disease: | ||
Population Age: Children, Under 18 | Gender: Male, Female | |
Trial protocol: Outside EU/EEA | ||
Trial results: View results |
EudraCT Number: 2017-001044-35 | Sponsor Protocol Number: GQM00016 | Start Date*: 2019-02-08 |
Sponsor Name:Sanofi Pasteur SA | ||
Full Title: Immunogenicity and Safety of a Multi-Dose Quadrivalent Influenza Vaccine in Children Aged 6 months to 17 Years | ||
Medical condition: Prophylaxis of influenza (Northern Hemisphere 2017-2018 season) in children aged 6 months to 17 years | ||
Disease: | ||
Population Age: Infants and toddlers, Children, Adolescents, Under 18 | Gender: Male, Female | |
Trial protocol: Outside EU/EEA | ||
Trial results: View results |
EudraCT Number: 2006-006949-13 | Sponsor Protocol Number: BRD/06/162 | Start Date*: 2007-10-16 | |||||||||||
Sponsor Name:University College London | |||||||||||||
Full Title: A multi-centre exploratory study to evaluate the efficacy of the dopamine receptor agonist rotigotine in the treatment of hemispatial neglect and motor deficits following stroke. | |||||||||||||
Medical condition: Hemispatial neglect and motor deficits following right-hemisphere stroke. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2017-000755-97 | Sponsor Protocol Number: EPFL-CNBI-2017-01 | Start Date*: 2017-03-16 |
Sponsor Name:Defitech Chair in Brain-Machine Interface, EPFL | ||
Full Title: Brain-computer interface and neuromuscular stimulation for rehabilitation following chronic stroke | ||
Medical condition: I61 - Intracerebral haemorrhage I63 - Cerebral infarction Chronic condition (at least 10 months after occurrence of cerebrovascular accident) | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: Outside EU/EEA | ||
Trial results: (No results available) |
EudraCT Number: 2007-001465-14 | Sponsor Protocol Number: CSLCT-NHF-06-30 | Start Date*: 2007-05-17 |
Sponsor Name:CSL Limited | ||
Full Title: A Single Centre, Open-Label Study to Evaluate the Immunogenicity and Safety of Enzira Vaccine in Healthy Adults aged ≥ 18 to < 60 years and in Healthy Older Adults aged ≥ 60 years for the 2007/2008... | ||
Medical condition: Prophylaxis of Influenza | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (Completed) | ||
Trial results: View results |
EudraCT Number: 2005-000651-14 | Sponsor Protocol Number: CSLCT-NHF-04-99 | Start Date*: 2005-05-27 |
Sponsor Name:CSL Limited | ||
Full Title: A Single Site, Open-Label Study to Evaluate the Immunogenicity and Safety of Influenza Vaccine, CSL Limited in Healthy 'Adults' aged >18 to <60 years and in Healthy 'Older Adults' aged >60 years fo... | ||
Medical condition: The vaccine is indicated for the prophylaxis of influenza | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (Completed) | ||
Trial results: View results |
EudraCT Number: 2008-001422-14 | Sponsor Protocol Number: CSLCT-NHF-07-49 | Start Date*: 2008-04-29 |
Sponsor Name:CSL Limited | ||
Full Title: A Single Centre, Open-Label Study to Evaluate the Immunogenicity and Safety of Enzira® vaccine in Healthy ‘Adults’ aged ≥ 18 to < 60 years and in Healthy ‘Older Adults’ aged ≥ 60 years for the 2008... | ||
Medical condition: Prophylaxis of influenza | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (Completed) | ||
Trial results: View results |
EudraCT Number: 2006-002068-25 | Sponsor Protocol Number: CSLCT-NHF-05-13 | Start Date*: 2006-05-23 |
Sponsor Name:CSL Limited | ||
Full Title: A Single Site, Open-Label Study to Evaluate the Immunogenicity and Safety of Enzira in Healthy 'Adults' aged >18 to <60 years and in Healthy 'Older Adults' aged >60 years for the 2006/2007 Northern... | ||
Medical condition: Prophylaxis of influenza | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (Completed) | ||
Trial results: View results |
EudraCT Number: 2006-002680-18 | Sponsor Protocol Number: 107975 | Start Date*: 2006-08-03 |
Sponsor Name:GlaxoSmithKline Biologicals | ||
Full Title: A phase II, controlled, randomized, single blind study to evaluate the immunogenicity, safety and reactogenicity of the low dose influenza vaccine adjuvanted with AS03 compared to Fluarix™ (GlaxoSm... | ||
Medical condition: Immunization against influenza in male and female subjects aged 60 years and older. | ||
Disease: | ||
Population Age: Elderly | Gender: Male, Female | |
Trial protocol: BE (Completed) | ||
Trial results: View results |
EudraCT Number: 2010-023105-35 | Sponsor Protocol Number: IC/VG/P01-2010 | Start Date*: 2010-10-14 |
Sponsor Name:Cantacuzino National Institute of Research and Development for Microbiology and Immunology | ||
Full Title: The Study of the Immunogenity and Reactogenity of Trivalent, Purified, Inactivated Influenza Vaccine for Parenteral Administration in Adults, for the 2010-2011 Season, Produced by Cantacuzino Natio... | ||
Medical condition: Healthy adult volunteers (2 age-groups: 18-60 years and >60 years old) are vaccinated in order to achieve protection against influenza virus infection with the vaccine containing the influenza viru... | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: RO (Ongoing) | ||
Trial results: (No results available) |
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