Catalyst Wire Dossier Catalyst Wire Dossier
FDA approval · 2018-12-11

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

View source ↗

Summary

The FDA approved a supplemental application for ZEVALIN (ibritumomab tiuxetan) submitted 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)