Immunogenicity and safety of orally administered killed whole cell non-typeable Haemophilus influenzae (Study HI-H003)
A single centre, double blind, placebo controlled, prospective study to assess the immunogenicity and safety of orally administered killed whole cell non-typeable Haemophilus influenzae (NTHi) HI-1-164 in smokers at risk of recurrent bronchitis (Study HI-H003)
The University of Newcastle Research Associates (TUNRA) Ltd
64 participants
Jul 25, 2005
Interventional
Conditions
Summary
This study monitored safety and measured specific and non-specific immunological parameters in smokers, who are a group at risk of recurrent bronchitis. This group was chosen rather than healthy non-smoking volunteers for this safety/pharmacokinetic study as it was thought possible that the immune parameters may differ in smokers to that in healthy non-smokers. This safety and immunogenicity study has been completed. It was not registered prior to initiation due to our unawareness of the registration system at that time. As it is a Phase I study and is not required to be registered it is being registered for the purpose of public information as we are now aware that post-initiation registration is possible
Eligibility
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Interventions
The test product was formalin-inactivated whole cell non-typeable Haemophilus influenzae formulated in enteric-coated tablets to be taken orally. Each tablet contained 45mg of active ingredient plus excipients. Three courses of tablets were taken by each participant at monthly intervals. Each course consisted of 2 tablets per day for three consecutive days. Thus treatment took place over a period of 60 days. Participants attended visits at 2-week intervals for 3 months.
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ACTRN12607000271404