WHO ICTRP trial

A phase II, controlled, single centre, open study to evaluate the safety…

EUCTR2007-002783-10-BE · EU Clinical Trials Register · Not Recruiting

Key facts

Trial ID EUCTR2007-002783-10-BE
Public title A phase II, controlled, single centre, open study to evaluate the safety, reactogenicity and immunogenicity of a second vaccination with the low dose influenza vaccine adjuvanted with a reduced dose of AS03, compared to a second dose of Fluarix™ (GlaxoSmithKline Biologicals) administered intramuscularly in subjects 18-60 years previously vaccinated in FLU-LD-004 clinical trial. - FLU-LD-010 EXT: 004 Y1
Scientific title A phase II, controlled, single centre, open study to evaluate the safety, reactogenicity and immunogenicity of a second vaccination with the low dose influenza vaccine adjuvanted with a reduced dose of AS03, compared to a second dose of Fluarix™ (GlaxoSmithKline Biologicals) administered…
Primary sponsor GlaxoSmithKline Biologicals
Registry EU Clinical Trials Register
Recruitment status Not Recruiting
Study type Interventional clinical trial of medicinal product
Countries Belgium
Conditions Re-vaccination against influenza in male and female subjects aged 18-60 years old.
Interventions Product Name: GlaxoSmihKline Biologicals low dose influenza vaccine adjuvanted with AS03 (half dose of AS03) Product Code: Flu-LD Pharmaceutical Form: Emulsion for injection INN or Proposed INN: Haemagglutinin from A/Solomon Islands/3/2006…
Registration date Aug 20, 2007
Target size 300
Secondary IDs 110674
Registry page clinicaltrialsregister.eu

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Source: World Health Organization (WHO), International Clinical Trials Registry Platform (ICTRP) · Source date:

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