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RECRUITING
NCT07570394

BREZTRI REGULATORY POST MARKETING SURVEILLANCE IN KOREA

Sponsor: AstraZeneca

View on ClinicalTrials.gov

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