Evusheld Japan PMS_Japan Post-Marketing Surveillance (PMS)

NCT05687877 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 366

Last updated 2026-01-08

No results posted yet for this study

Summary

To investigate intends to evaluate the incidence of adverse drug reactions (ADRs) in individuals who receive Evusheld in clinical practice to determine its post-marketing safety profile in Japanese.

Conditions

Sponsors & Collaborators

Principal Investigators

  • Toshimitsu Tokimoto · AstraZeneca KK

Eligibility

Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2023-01-06
Primary Completion
2025-01-20
Completion
2025-01-20

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 NCT05687877 on ClinicalTrials.gov