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Study of Immune Responses to Influenza Vaccination

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University of Pennsylvania

Status and phase

Enrolling
Phase 4

Conditions

Influenza Vaccination

Treatments

Biological: Influenza vaccination

Study type

Interventional

Funder types

Other

Identifiers

Details and patient eligibility

About

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.

Enrollment

75 estimated patients

Sex

All

Ages

18+ years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

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

Exclusion criteria

  • febrile illness at time of vaccination
  • active malignancy
  • use of immunosuppressing medications
  • blood donation in the past 60 days
  • influenza vaccinated during the preceding 6 months
  • allergic reactions to influenza vaccination

Trial design

Primary purpose

Basic Science

Allocation

N/A

Interventional model

Single Group Assignment

Masking

None (Open label)

75 participants in 1 patient group

Influenza vaccination cohort
Experimental group
Description:
Adults will receive one intramuscular dose of seasonal quadrivalent inactivated influenza vaccine, as indicated for standard of care.
Treatment:
Biological: Influenza vaccination

Trial contacts and locations

1

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Central trial contact

E.John Wherry, PhD; Sokratis Apostolidis, MD

Data sourced from clinicaltrials.gov

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