SPECIAL INVESTIGATION FOR ABRYSVO IN PREGNANT WOMEN AND INFANTS

NCT06482099 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 497

Last updated 2026-04-09

No results posted yet for this study

Summary

This post-marketing study is a multicenter cohort study in pregnant women vaccinated with Abrysvo (RSV vaccine)designed to confirm the safety in pregnant women and their infants under actual clinical practice in Japan.

Conditions

  • Respiratory Tract Infection

Interventions

BIOLOGICAL

RSVpreF vaccine

Injection in the muscle, 1 dose 0.5mL

Sponsors & Collaborators

Principal Investigators

  • Pfizer CT.gov Call Center · Pfizer

Eligibility

Min Age
0 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2024-10-01
Primary Completion
2026-02-27
Completion
2026-02-27

Countries

  • Japan

Study Locations

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Entities

Companies

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 NCT06482099 on ClinicalTrials.gov