All clinical trials on the European Union Clinical Trials Register (EUCTR) must report their results in the registry within a year of completion. This site tracks who's doing this and who isn't. Learn more »
These trials completed more than 12 months ago and should have reported results.
These trials are not yet due to report results: some are ongoing, some completed within the past 12 months.
These trials have problematic data on the registry. Details why »
Status | Trial ID | Title | Completion date | Category |
---|---|---|---|---|
Reported results | 2004-001600-12 | Fluval AB Vaccine Serologic Clinical Trial | 2004-10-15 | due-trials |
Reported results | 2005-002705-23 | FluvalAB Influenza Vaccine Serologic Clinical Trial for 2005-2006 Influenza Season | 2005-10-20 | due-trials |
Reported results | 2006-002789-20 | FluvalAB Influenza Vaccine Serologic Clinical Trial for 2006-2007 Influenza Season | 2006-10-14 | due-trials |
Reported results | 2007-002614-19 | FluvalAB Seasonal Influenza Vaccine Serologic Clinical Trial for 2007-2008 Influenza Season | 2007-10-06 | due-trials |
Reported results | 2008-003655-74 | FluvalAB Seasonal Influenza Vaccine Serologic Clinical Trial for 2008-2009 Influenza Season | 2008-09-29 | due-trials |
Completed, but no date, and reported results | 2009-012555-22 | Serologic Study of FluvalAB Influenza Vaccine (Trivalent, Seasonal) intended to Use in the 2009-2010 Vaccination Season | bad-data | |
Reported results | 2009-014765-74 | Tolerability and Safety Study of Fluval P Monovalent Influenza Vaccine in Children | 2010-06-03 | due-trials |
Reported results | 2009-014807-30 | Tolerability and Immunogenicity Study of Fluval P Monovalent Influenza Vaccine in Children and Adolescents | 2010-06-03 | due-trials |
Reported results | 2010-021071-83 | Tolerability and Immunogenicity Study of FluvalAB Influenza Vaccine (trivalent, seasonal, active ingredient content: 15 μg HA/strain/0.5 mL) in Adults and Elderly Person | 2010-10-26 | due-trials |
Reported results | 2011-002158-30 | Tolerability and Immunogenicity Study of Fluval AB Influenza Vaccine (trivalent, seasonal, active ingredient content: 15 μg HA/strain/0.5 mL) in Adults and Elderly Persons | 2011-08-24 | due-trials |
Reported results | 2011-003166-32 | A Randomized, Double-blind, Multi-Center Study to Evaluate Safety and Immunogenicity of One Dose of Four FLUVAL AB-like (Trivalent, Whole Virus, Aluminium Phosphate Gel Adjuvanted) Influenza Vaccines ... | 2011-10-17 | due-trials |
Reported results | 2011-003314-16 | A Randomized, Active Controlled, Double-blind, Multi-Centre Study to Evaluate Safety and Immunogenicity of One Dose of FLUVAL AB-like (Trivalent, Whole Virus, Aluminium Phosphate Gel Adjuvanted) Influ... | 2012-03-21 | due-trials |
Reported results | 2012-002379-32 | Tolerability and Immunogenicity Study of FLUVAL AB Influenza Vaccine (trivalent, seasonal, active ingredient content: 15 μgHA/strain/0.5 mL) in Adults and Elderly Persons | 2012-09-19 | due-trials |
Reported results | 2013-002153-30 | Tolerability and Immunogenicity Study of FLUVAL AB Influenza Vaccine (trivalent, seasonal, active ingredient content: 15 μgHA/strain/0.5 mL) for the Use in the Season 2013/2014 in Adults and Elderly S... | 2013-09-17 | due-trials |
Reported results | 2013-003449-40 | Immunogenicity and Tolerability Study of FLUVAL AB Novo Suspension for Injection (trivalent, seasonal influenza vaccine, active ingredient content: 6 μg HA/strain/0.5 ml) for Children and Adolescents | 2014-12-09 | due-trials |