FDA Approved: TASIGNA — Supplemental Application (Novartis Pharmaceuticals Corporation)

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Summary

FDA approved a supplemental application for Tasigna (nilotinib) from Novartis, outlining changes to the drug’s labeling.

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Diseases / indications

• Acute Lymphoblastic Leukemia
• Chronic Myeloid Leukemia

Drugs mentioned

• Tasigna (nilotinib)

Snippet

SUPPL AP for TASIGNA (NILOTINIB)