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Clinical Trials in the USA / NCT06782282
Active, not recruiting Observational

A Study to Learn About How Well the Prevnar 20 Vaccine Works for Pneumonia in People Who Are 65 Years and Older

NCT06782282 · tracked via the Priya Life Science USA tracker
Sponsor
Pfizer
Phase
Observational
Started
2025-01-20
Last updated
2026-04-22

Condition(s) studied

Community-Acquired Pneumonia (CAP)

Study summary

The purpose of this study is to learn about how well the Prevnar 20 vaccine (PCV20) stops invasive pneumococcal disease (a group of severe infections caused by a bacteria called Streptococcus pneumoniae), pneumococcal pneumonia (a bacterial lung disease caused by the germ Streptococcus pneumoniae), all-cause pneumonia (pneumonia caused by any germ including bacteria, a virus, or a fungus), and lower respiratory tract infection (infection of the lower airways in the lung) in people 65 years and older.

This study will use a database of people who have Medicare insurance with names and other identifying information removed. This study will include people who:

* are 65 years and older,
* live in one of the 50 United States or Washington DC, and
* are enrolled in Medicare Fee-for-Service Parts A and B for at least 1 year.

The study uses data that is already being collected and no treatment or vaccine will be given in the study.

People that fit the description above will be followed in the Medicare database for about two years. Their information will be reviewed to see if they had vaccines for pneumonia or had certain health events, such as pneumonia or lower respiratory tract infection.

The experiences of people that received Prevnar 20 will be compared to the experiences of people that did not receive the vaccine. This will help to show how well Prevnar 20 works at stopping invasive pneumococcal disease, pneumococcal pneumonia, all-cause pneumonia, and lower respiratory tract infection.

Eligibility

Sex
ALL
Min age
65 Years
Max age
—
Healthy volunteers
No
Patients from the Medicare database to be included in the analysis must be: * aged 65 or older as of 28Jan22 (date of 20-valent pneumococcal conjugate vaccine (PCV20) * residing in one of the 50 US states or Washington DC * be continuously enrolled in Medicare Fee for Service Parts A and B for 365 days prior to the index date allowing for gaps of up to 45 days (baseline period) Patients from the Medicare database will be excluded from the analysis if: * there is a record of death prior to the index date * the patient was enrolled in Medicare Part C at any point between 28Jan22 and the index date * the patient received PCV20 before 01Jul22 * the patient received PCV15 prior to the index date * sex information is missing If the patient received the pneumococcal polysaccharide vaccine (PPSV23) within 2 years prior to index date, the corresponding time segment (ie 2 years prior to index date) will be excluded. If the patient received PCV13 within the past 5 years prior to the index date, the corresponding time segment (ie 5 years prior to index date) will be excluded. However, those who received PCV13 more than 5 years prior to index date will still have all data included in primary analyses. For PCV20 period, exclude those when IPD, PP, ACP or LRTI outcome incurred between PCV20 vaccination date and prior to the index date (a 30-day blackout period).

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
Pfizer United States New York New York

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Other trials for the same condition

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT06782282 on ClinicalTrials.gov ↗ ← All trials in the USA