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FDA approval · 2025-04-09

FDA Approved: VITRAKVI — Supplemental Application (Loxo Oncology, Inc.)

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Summary

FDA approved a supplemental application for VITRAKVI (larotrectinib) to expand its labeling for patients with solid tumors that harbor NTRK gene fusions.

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Diseases / indications

Drugs mentioned

  • Vitrakvi (larotrectinib)

Snippet

SUPPL AP for VITRAKVI (LAROTRECTINIB)