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Effectiveness of BNT162b2 Formulations Using State Vaccine Registry and Insurance Claims Data

Pfizer logo

Pfizer

Status

Completed

Conditions

COVID-19 Vaccines
SARS-CoV-2

Treatments

Biological: Vaccination

Study type

Observational

Funder types

Industry

Identifiers

NCT06199934
RAVEN
C4591065

Details and patient eligibility

About

The primary purpose of this study is to learn about how well different versions of the Pfizer-BioNTech COVID-19 vaccine (called BNT162b2) work at preventing death, severe COVID-19 that requires a trip to the hospital, and overall use of healthcare resources, such as needing to go the doctor or urgent care due to illness. Pfizer is not enrolling any participants for this study. Instead, existing data from different health data sources will be used to help answer the scientific questions Pfizer is interested in learning more about.

Enrollment

1 patient

Sex

All

Volunteers

No Healthy Volunteers

Inclusion criteria

  • People with at least one year of pharmacy and medical enrollment in HealthVerity prior to vaccine availability
  • State of California or Louisiana resident for at least one year

Exclusion criteria

  • People currently pregnant,
  • Individuals with discrepancies in sex and/or year of birth between HealthVerity claims and California/Louisiana immunization registry datasets
  • A diagnosis of COVID-19 in any setting ≤ 90 days prior to start of study or receipt COVID-19 vaccine ≤ 90 days prior to start of study.

Trial design

1 participants in 2 patient groups

Vaccinated
Description:
BNT162b2 recipients
Treatment:
Biological: Vaccination
Unvaccinated
Description:
BNT162b2 eligible but did not receive

Trial contacts and locations

1

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Central trial contact

Pfizer CT.gov Call Center

Data sourced from clinicaltrials.gov

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