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FDA approval · 2025-10-01

FDA Approved: VONJO — Supplemental Application (Sobi, Inc.)

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Summary

The FDA approved a supplemental application for VONJO (pacritinib) from Sobi, Inc., expanding its labeling for the treatment of adults with myelofibrosis.

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Diseases / indications

Drugs mentioned

  • VONJO (pacritinib)

Snippet

SUPPL AP for VONJO (PACRITINIB)