Catalyst Wire Dossier Catalyst Wire Dossier
FDA approval · 2026-04-07

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

View source ↗

Summary

FDA approved a supplemental application for PLUVICTO (lutetium Lu-177 vipivotide tetraxetan) from Novartis, signaling an updated regulatory status for this ther…

Upgrade for the full analysis, importance score, and drug timeline.

Diseases / indications

Drugs mentioned

  • Pluvicto (lutetium-177 PSMA-617)

Snippet

SUPPL AP for PLUVICTO (LUTETIUM LU 177 VIPIVOTIDE TETRAXETAN)