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Home » Neurocrine Biosciences Announces FDA Approval of CRENESSITY

Neurocrine Biosciences Announces FDA Approval of CRENESSITY

CRENESSITY, the first new treatment available in 70 years to the classic congenital adrenal hyperplasia (CAH) community, offers a paradigm-shifting treatment approach.
FDA approval supported by data from the largest-ever clinical trial program in pediatric and adult patients with classic CAH.
CRENESSITY is expected to be commercially available in approximately one week
Rare Pediatric Disease Priority Review Voucher granted in connection with approval.

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