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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