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Crinecerfont in Adults With Classic Congenital Adrenal Hyperplasia
2023-509171-16-00Phase 3Authorised
- Sponsor
- Neurocrine Biosciences
- Start
- Jul 2024
- Modality
- Small Molecules
- Countries
- 16
01
Overview
Phase 3, randomised, double-blind trial in 21-hydroxylase deficiency (21-OHD) comparing Crinecerfont with Placebo (2 arms). Primary endpoint: Percent change from baseline in glucocorticoid daily dose at Week 24. Planned start Jul 2024; status: authorised.
02
Drugs
crinecerfont
03
Conditions
21-hydroxylase deficiency (21-OHD)
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