US FDA Approves ZANVASTRO as First Disease-Modifying Treatment for Alexander Disease
The US Food and Drug Administration (FDA) approves ZANVASTRO (zilganersen) as the first disease-modifying treatment for Alexander Disease (AxD) in pediatric and adult patients.
Priority Review Voucher (PRV) | 05/09/2026 | By News Bureau
Atossa Therapeutics receives US Food and Drug Administration (FDA) Rare Pediatric Disease designation for (Z)-Endoxifen in McCune-Albright syndrome, qualifying for Priority Review Voucher award upon approval.
Priority Review Voucher (PRV) | 05/05/2026 | By News Bureau | 150
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