Study of Immune Responses to Influenza Vaccination

Trial statusRecruiting
Trial phasePhase 4
Trial typeInterventional
Biological sexAll
Age18+
SponsorUniversity of Pennsylvania

About this trial

Better understanding of the immune responses to influenza vaccination is needed in order to understand situations of poor vaccine response. Adults will receive influenza vaccination and then have peripheral blood drawn at pre-defined intervals in order to study the lymphocyte responses.

Eligibility criteria

This trial accepts healthy volunteers

Qualifiers

Community-dwelling adults able to provide consent who need influenza vaccination for standard of care

Disqualifiers

febrile illness at time of vaccination

active malignancy

use of immunosuppressing medications

blood donation in the past 60 days

Trial design

Design model

Single group

Treatments tested in this trial

  • Influenza vaccination

    Biological/Vaccine

    Adults will receive one intramuscular dose of seasonal quadrivalent inactivated influenza vaccine, as indicated for standard of care.

Treatment groups

75 Participants
are divided into 1 treatment group
Group A: Influenza vaccination cohortExperimental treatment 1 intervention

Trial outcomes

Primary outcomes

1

Influenza neutralizing antibody titers

Time frame
21-42 days

Secondary outcomes

Other outcomes

Sponsors and contacts

Click on the lead sponsor to view all of their trials.