GlaxoSmithKline (GSK) has provided results from its first clinical trial assessing use of its pandemic (H1N1) adjuvanted vaccine. The results demonstrate that after one dose the candidate vaccine can provide a strong immune response which exceeds the immunogenicity criteria as defined by international licensing authorities for a pandemic influenza vaccine.
Reportedly, the trial involves 130 healthy volunteers aged 18 to 60 years old, and has been designed to evaluate the tolerability and immunogenicity of GSK’s split-virus pandemic (H1N1) adjuvanted vaccine in comparison with an unadjuvanted test study formulation.
In the trial, the antigen content of the adjuvanted vaccine is 5.25ug and in the unadjuvanted vaccine is 21ug. The antigen content of the adjuvanted vaccine is comparable to the expected final formulation of the adjuvanted vaccine of 3.75ug.
Results of the adjuvanted vaccine demonstrated that hemagglutination-inhibition titres exceeded the regulatory threshold, with a 1:40 seroconversion in more than 98% of subjects receiving the first dose. In the unadjuvanted group, 95% of the subjects reached the same threshold. These results were obtained 3 weeks following vaccination.
The company said that it is conducting a further 15 studies in over 9000 subjects including healthy adults, the elderly and children (including infants) across Europe, Canada and the US to evaluate its pandemic (H1N1) adjuvanted vaccine.
Jean Stephenne, president of GlaxoSmithKline Biologicals, said: “This trial provides encouraging data on the potential use of a single dose of our pandemic vaccine. We have shared these data with both regulatory authorities and governments who are making key decisions on urgent global public healthcare at this time. Our next step is to complete this trial, as well as 15 other studies in our clinical development programme for the vaccine.”