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A Phase 3b, Open-Label Study of Crinecerfont to Evaluate Androgen Reduction and Related Outcomes in Adults With Classic Congenital Adrenal Hyperplasia

Status
Not yet recruiting
Phases
Phase 3
Study type
Interventional
Source
EU CTIS
Registry ID
CTIS2025-524282-24-00
Enrollment
47
Registered
2026-07-23
Start date
Unknown
Completion date
Unknown
Last updated
2026-07-24

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Classic Congenital Adrenal Hyperplasia (CAH)

Brief summary

Change from baseline in pre-GC serum androstenedione at Week 24.

Detailed description

Not applicable

Interventions

Sponsors

Neurocrine Biosciences Inc.
Lead SponsorINDUSTRY

Eligibility

Sex/Gender
All
Age
18 Years to 64 Years

Design outcomes

Primary

MeasureTime frame
Change from baseline in pre-GC serum androstenedione at Week 24.

Secondary

MeasureTime frame
Not applicable

Outcome results

None listed

Source: EU CTIS · Data processed: Jul 25, 2026