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RECRUITING
NCT07755826

Repotrectinib Post-Marketing Surveillance in Pediatric Patients With NTRK Fusion-Positive Tumors in Japan

Sponsor: Bristol-Myers Squibb

View on ClinicalTrials.gov

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

Interventions

DRUG

Repotrectinib

As per product label

Locations (2)

CMIC Co., Ltd.

Minato-ku, Tokyo, Japan

EPS Corporation

Tokyo, Japan