Crysvita® (burosumab-twza)

BL 761068

Crysvita® (burosumab-twza)

BL 761068

U.S. License Holder:

Ultragenyx Pharmaceutical Inc.

Date of License:

April-17-2018

Last Update:

Nov-15-2024

approved_indications FDA-Approved Indications

CRYSVITA (burosumab-twza) is a fibroblast growth factor 23 (FGF23) blocking antibody indicated for:

The treatment of X-linked hypophosphatemia (XLH) in adult and pediatric patients 6 months of age and older;

The treatment of FGF23-related hypophosphatemia in tumor-induced osteomalacia (TIO) associated with phosphaturic mesenchymal tumors that cannot be curatively resected or localizedin adult and pediatric patients 2 years of age and older.

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Methodology

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