Catalyst Wire Dossier Catalyst Wire Dossier
FDA approval · 2026-07-31

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

View source ↗

Summary

Supplemental application for PLUVICTO (lutetium Lu-177 vipivotide tetraxetan) submitted by Novartis Pharmaceuticals Corporation.

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)