This is a Phase 3 study to evaluate the efficacy, safety, and tolerability of crinecerfont versus placebo administered for 24 weeks in approximately 165 adult subjects with classic CAH due to 21-hydroxylase deficiency. The study consists of a 6 month randomized, double blind, placebo-controlled period, followed by 1 year of treatment with crinecerfont. Duration of participation is approximately 20 months.
| Condition | Congenital Adrenal Hyperplasia |
|---|---|
| Treatment | Placebo, Crinecerfont |
| Clinical Study Identifier | NCT04490915 |
| Sponsor | Neurocrine Biosciences |
| Last Modified on | 25 August 2023 |
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