FDA Approved: ICLUSIG — Supplemental Application (Takeda Pharmaceuticals America, Inc.)

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Summary

FDA approved a supplemental application for ICLUSIG (ponatinib hydrochloride) submitted by Takeda Pharmaceuticals America, Inc., under NDA 203469. The approval …

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Diseases / indications

• Acute Lymphoblastic Leukemia
• Chronic Myeloid Leukemia

Drugs mentioned

• Iclusig (ponatinib)

Snippet

SUPPL AP for ICLUSIG (PONATINIB HYDROCHLORIDE)