Renal

Classic congenital adrenal hyperplasia due to 21-hydroxylase deficiency, simple virilizing form

0

studies recruiting now

as of 7 Sept 2026

0

studies registered in total

as of 7 Sept 2026

0

countries with a recruiting site

as of 7 Sept 2026

None

recruiting study posted to date

among recruiting studies

Recruiting trials

No registered studies found for Classic congenital adrenal hyperplasia due to 21-hydroxylase deficiency, simple virilizing form.

ClinicalTrials.gov has no study listed under this name as of 7 Sept 2026. That can change, and there are other routes worth knowing about.

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Patient organisations

We do not yet list a dedicated organisation for this condition. The directories below are the best route.

About Classic congenital adrenal hyperplasia due to 21-hydroxylase deficiency, simple virilizing form

RareTrial does not yet hold a plain-language description of this condition. The most reliable starting point is Orphanet’s expert page, which lists specialist centres, registries and patient organisations, and the gene involved (CYP21A2).

Treatments being studied

2 approved treatments and 6 in clinical development, from Open Targets (CC BY 4.0). Not medical advice.

Approved: Hydrocortisone (Acetasol hc)Approved: Crinecerfont (Crenessity)
Phase 2Fludrocortisone Acetate (Astonin)
Phase 2Tildacerfont
Phase 2Abiraterone Acetate (Abiraterone accord)
Phase 2Nevanimibe Hydrochloride
Phase 1/2Nifedipine (Adalat)
Phase 1Verucerfont

Related conditions

Information, not medical advice. Trial listings are shown as recorded on ClinicalTrials.gov; whether any study is right for you is a decision for you and your clinicians, and eligibility is decided by each research team. Disease information from Orphanet (CC BY 4.0).