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FDA Approves Vitrakvi for Solid Tumors with NTRK Gene Fusions
November 29, 2018The Food and Drug Administration (FDA) has granted accelerated approval to larotrectinib (Vitrakvi, Loxo Oncology and Bayer) for adult and pediatric patients with ..... -
FDA approves an oncology drug that targets a key genetic driver of cancer, rather than a specific type of tumor
November 28, 2018The U.S. Food and Drug Administration today granted accelerated approval to Vitrakvi (larotrectinib), a treatment for adult and pediatric patients whose cancers have a specific genetic feature (biomarker).
Pharma Sources Insight January 2025
