Catalyst Wire Dossier Catalyst Wire Dossier
FDA approval · 2008-03-25

FDA Approved: ZEVALIN — Supplemental Application (Acrotech Biopharma Inc)

View source ↗

Summary

FDA has approved a supplemental application for Zevalin (ibritumomab tiuxetan) filed by Acrotech Biopharma Inc.

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

Diseases / indications

Drugs mentioned

  • Zevalin (ibritumomab tiuxetan)

Snippet

SUPPL AP for ZEVALIN (IBRITUMOMAB TIUXETAN)