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Repotrectinib Post-Marketing Surveillance in Pediatric Patients With NTRK Fusion-Positive Tumors in Japan
Sponsor: Bristol-Myers Squibb
Summary
This study will collect safety information during routine medical care for children and adolescents in Japan who have been diagnosed with NTRK fusion-positive advanced or recurrent solid tumors who start treatment with repotrectinib. The study will describe how often side effects occur during treatment, with special attention to central nervous system disorders, interstitial lung disease, and fractures.
Official title: Repotrectinib Post-Marketing Surveillance in Pediatric Patients (Age 4 to < 18) With NTRK Fusion-Positive Advanced/Recurrent Solid Tumors in Japan
Key Details
Gender
All
Age Range
4 Years - 17 Years
Study Type
OBSERVATIONAL
Enrollment
20
Start Date
2025-11-20
Completion Date
2034-04-30
Last Updated
2026-08-10
Healthy Volunteers
No
Conditions
Interventions
Repotrectinib
As per product label
Locations (2)
CMIC Co., Ltd.
Minato-ku, Tokyo, Japan
EPS Corporation
Tokyo, Japan