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NOT YET RECRUITING
NCT07599007

Repotrectinib Post-Marketing Surveillance in Korean Patients With ROS1-Positive Non-Small Cell Lung Cancer (NSCLC) or Solid Tumors Harboring a Neurotrophic Tyrosine Receptor Kinase (NTRK) Gene Fusion

Sponsor: Bristol-Myers Squibb

View on ClinicalTrials.gov

Summary

This observational study evaluates the real-world safety and effectiveness of repotrectinib in Korean participants with locally advanced or metastatic ROS1-positive non-small cell lung cancer or solid tumors harboring neurotrophic tyrosine receptor kinase (NTRK) gene fusions. Participants receiving repotrectinib in routine clinical practice will be followed for up to 12 months or until the end of the 2-year surveillance period, whichever occurs first.

Official title: AUGTYRO™ (Repotrectinib) Post-Marketing Surveillance in Korean Patients With Locally Advanced or Metastatic Ros1-Positive NSCLC or Solid Tumors Harboring a NTRK Gene Fusion

Key Details

Gender

All

Age Range

12 Years - Any

Study Type

OBSERVATIONAL

Enrollment

10

Start Date

2026-05-24

Completion Date

2028-01-31

Last Updated

2026-05-20

Healthy Volunteers

No

Interventions

DRUG

Repotrectinib

As per product label

Locations (1)

Bristol Myers Squibb Pharmaceutical Korea Ltd

Seoul, South Korea