A Two-arm, Non-randomised, Open-label Experimental Medicine Study to Compare Immune Responses Between Healthy Volunteers Aged 18-40years Receiving Either an Intranasal Live-attenuated Influenza Vaccine or Viral Challenge With GMP Influenza A/Belgium/4217/2015 (H3N2)

Status: Recruiting
Location: See location...
Intervention Type: Biological
Study Type: Interventional
Study Phase: Not Applicable
SUMMARY

This experimental medicine study aims to compare immune responses in healthy adult volunteers aged 18-40 years against influenza vaccination and infection in the upper and lower respiratory tract, following administration of a live-attenuated influenza vaccine delivered by nasal spray versus influenza A (H3N2) viral challenge.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Maximum Age: 40
Healthy Volunteers: t
View:

• Adults aged between 18-40 years inclusive

• Sero-suitable as defined by a serum micro-neutralisation titre \<1:20

• Female participant who is not of child-bearing potential as assessed by an investigator OR is willing and able to use contraception as described in the protocol

• Male participants who are willing to use one of the contraception methods described in the protocol

• In good health with no clinically significant medical conditions

Locations
Other Locations
United Kingdom
Imperial Clinical Research Facility, Imperial College Healthcare NHS Trust
RECRUITING
London
Contact Information
Primary
Polly Fox, MSc
polly.fox@imperial.ac.uk
0208383 3231
Time Frame
Start Date: 2025-04-16
Estimated Completion Date: 2026-01-06
Participants
Target number of participants: 36
Treatments
Experimental: LAIV
Experimental: IAV Challenge
Related Therapeutic Areas
Sponsors
Collaborators: Imperial College Healthcare NHS Trust
Leads: Imperial College London

This content was sourced from clinicaltrials.gov

Similar Clinical Trials