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Crinetics Pharmaceuticals

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FDA designations

  • Crinetics Secures FDA Orphan Drug Designation for Atumelnant in Treating Congenital Adrenal HyperplasiaAug 21, 2025

News

  • Crinetics Pharmaceuticals received European Commission approval of PALSONIFY for treating acromegaly in adultsApr 28, 2026
  • Crinetics initiated Phase 2/3 pediatric trial of atumelnant in congenital adrenal hyperplasiaJan 23, 2026
  • Crinetics reports strong PALSONIFY launch and positive Phase 2 atumelnant data showing lower androstenedione and reduced glucocorticoid doses in congenital adrenal hyperplasiaJan 5, 2026
  • Crinetics to provide PALSONIFY business update and announce topline results from fourth cohort of Phase 2 atumelnant trial in congenital adrenal hyperplasiaJan 5, 2026
  • Crinetics announced first patient dosed in Phase 1/2 trial evaluating CRN09682 for neuroendocrine tumors and somatostatin receptor 2-expressing tumorsDec 3, 2025

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