FDA Approved: CAPRELSA — Supplemental Application (Genzyme Corporation)

View source ↗

Summary

FDA approved a supplemental application for CAPRELSA (vandetanib) submitted by Genzyme Corporation. The supplemental submission has been approved.

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

Diseases / indications

• Medullary Thyroid Carcinoma

Drugs mentioned

• Caprelsa (vandetanib)

Snippet

SUPPL AP for CAPRELSA (VANDETANIB)