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RECRUITING
NCT04592523

A Study of Usage of Brigatinib in the Treatment of Adult Participants for Approved Indications In South Korea

Sponsor: Takeda

View on ClinicalTrials.gov

Summary

The purpose of this study is to estimate the proportion of all adverse events (AEs) including serious adverse events (SAEs) occurring with the use of brigatinib among adult participants who have been administered brigatinib as per the approved indications.

Official title: Post-Marketing Surveillance (Usage Results Study) of Brigatinib in the Treatment of Adult Patients for Approved Indications in South Korea

Key Details

Gender

All

Age Range

19 Years - Any

Study Type

OBSERVATIONAL

Enrollment

257

Start Date

2019-09-05

Completion Date

2026-08-26

Last Updated

2025-12-24

Healthy Volunteers

No

Interventions

OTHER

No Intervention

This is a non-interventional study.

Locations (1)

Pusan National University Hospital

Busan, South Korea