Neurocrine Biosciences launches Crenessity in USA
San Diego, USA-based Neurocrine Biosciences (Nasdaq: NBIX) today announced the launch of its Crenessity (crinecerfont) in the USA.
The drug was approved by the US Food and Drug Administration earlier this month as an adjunctive treatment to glucocorticoid replacement to control androgens in adult and pediatric patients four years of age and older with classic congenital adrenal hyperplasia (CAH).
"Individuals with CAH and their families have faced ongoing challenges with managing the condition with high-dose steroids alone for the past 70 years," said Kyle Gano, chief executive of Neurocrine Biosciences. "We're proud to now provide Crenessity to the community, and we are committed to supporting patients in obtaining treatment with Crenessity through our comprehensive assistance program."
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