Official Title
Effectiveness of BNT162b2 Formulations Using State Vaccine Registry and Insurance Claims Data
Brief Summary

The primary purpose of this study is to learn about how well different versions of thePfizer-BioNTech COVID-19 vaccine (called BNT162b2) work at preventing death, severeCOVID-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 enrollingany participants for this study. Instead, existing data from different health datasources will be used to help answer the scientific questions Pfizer is interested inlearning more about.

Detailed Description

Not Provided

Completed
SARS-CoV-2
COVID-19 Vaccines

Biological: Vaccination

BNT162b2 vaccination

Eligibility Criteria

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.

Eligibility Gender
All
Eligibility Age
Minimum: N/A ~ Maximum: N/A
Countries
United States
Locations

Pfizer Global Headquarters
New York 5128581, New York 5128638, United States

Pfizer CT.gov Call Center, Study Director
Pfizer

NCT Number
Keywords
Covid-19
XBB vaccine effectiveness
MeSH Terms
COVID-19
Vaccination