FDA
approval
· 2026-07-31
FDA Approved: PLUVICTO — Supplemental Application (Novartis Pharmaceuticals Corporation)
Summary
Supplemental application for PLUVICTO (lutetium Lu-177 vipivotide tetraxetan) submitted by Novartis Pharmaceuticals Corporation.
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Diseases / indications
Drugs mentioned
Snippet
SUPPL AP for PLUVICTO (LUTETIUM LU 177 VIPIVOTIDE TETRAXETAN)