Neurocrine’s Crinecerfont Draws Cautious Optimism On Clinical Meaningfulness

The biotech plans to file for approval for congenital adrenal hyperplasia (CAH) next year and is now looking ahead to a pediatric study, which may pose lower risk.

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Some questions remain around the clinical meaningfulness as well as the commercial opportunity based on Neurocrine Biosciences, Inc.’s Phase III CAHtalyst trial of crinecerfont in adults with classic congenital adrenal hyperplasia, but analysts expressed confidence given the study’s overall success and high degree of statistical significance.

The biotech company announced topline results on 12 September, saying that CAHtalyst met the primary endpoint, showing a statistically significant reduction in daily glucocorticoid use at week 24 compared with...

Key Takeaways
  • Neurocrine’s Phase III CAHtalyst trial of crinecerfont in congenital adrenal hyperplasia met its primary and key secondary endpoints.

  • Numerical data for the primary endpoint...

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