FDA
approval
· 2025-04-09
FDA Approved: VITRAKVI — Supplemental Application (Loxo Oncology, Inc.)
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
Snippet
SUPPL AP for VITRAKVI (LAROTRECTINIB)