Special Investigation for Booster Dose of Comirnaty in Children Ages 6 Months Though 4 Years

NCT06130410 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 25

Last updated 2025-07-14

Study results available
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Summary

The purpose of this post-marketing study is to assess the safety of Comirnaty monovalent XBB.1.5. for booster vaccination children ages 6 months though 4 years under actual use medical practice.

Conditions

Interventions

BIOLOGICAL

COMIRNATY intramuscular injection

Booster injection in the muscle, 1 dose

Sponsors & Collaborators

Principal Investigators

  • Pfizer CT.gov Call Center · Pfizer

Eligibility

Min Age
6 Months
Max Age
4 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2024-03-06
Primary Completion
2024-07-26
Completion
2024-07-26

Countries

  • Japan

Study Locations

More Related Trials

Entities

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT06130410 on ClinicalTrials.gov