Evusheld Japan PMS_Japan Post-Marketing Surveillance (PMS)
NCT05687877 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 366
Last updated 2026-01-08
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
- lead INDUSTRY
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
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