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BREZTRI REGULATORY POST MARKETING SURVEILLANCE IN KOREA
Sponsor: AstraZeneca
Summary
As part of a post-approval commitment requested by the Ministry of Food and Drug Safety (MFDS), this open-label, single-arm, multicentre, observational Post-Marketing Surveillance (PMS) study aims to characterize the safety profile of Breztri in real-world clinical practice settings, either confirming known safety outcomes or identifying previously unsuspected adverse drug reactions. The study will also evaluate effectiveness of Breztri in real-world clinical practice settings, generating essential clinical evidence from a broader and more diverse Korean patient population representative of daily medical practice.
Key Details
Gender
All
Age Range
Any - Any
Study Type
OBSERVATIONAL
Enrollment
600
Start Date
2026-09-17
Completion Date
2027-07-31
Last Updated
2026-09-23
Healthy Volunteers
No
Locations (10)
Research Site
Chuncheon, South Korea
Research Site
Daegu, South Korea
Research Site
Goyang-si, South Korea
Research Site
Gwangmyeong, South Korea
Research Site
Jinju, South Korea
Research Site
Seongnam-si, South Korea
Research Site
Seongnam-si, South Korea
Research Site
Seoul, South Korea
Research Site
Seoul, South Korea
Research Site
Wŏnju, South Korea