Cure My Disease

Don't miss your cure!

Home News Browse Soon ready About
Log in / Sign up

Non-classic congenital adrenal hyperplasia

MONDO:0023601

A milder form of congenital adrenal hyperplasia characterized by decreased activity of an enzyme in the steroidogenic pathway, typically presenting later in life, that does not require life-long cortisol replacement.

Also known as: late-onset congenital adrenal hyperplasia, non-classic congenital adrenal hyperplasia, LOCAH, NCCAH, attenuated congenital adrenal hyperplasia, non classic congenital adrenal hyperplasia

2 clinical trials for this condition and its sub-types.

Follow this condition — get notified about new trials

Broader categories

Disease (680) Metabolic disease (233) Inherited lipid metabolism disorder (189) Hereditary disease (176) Endocrine system disorder (72) Inborn errors of metabolism (45) Congenital adrenal hyperplasia (31) Adrenocortical insufficiency (26) Hereditary endocrine growth disease (24) Human disease (14)
Trials to join now! 1 Not yet recruiting 1
Sort by
  • New imaging tracer could shed light on adrenal cholesterol

    Knowledge-focused Recruiting now

    This study tests a special radioactive tracer called [18F]FNP-59 to see if it can safely and clearly show cholesterol activity in the adrenal gland using PET scans. About 24 people will take part, including healthy volunteers and those with known adrenal problems. The goal is to …

    Phase: EARLY_PHASE1 • Sponsor: Benjamin Viglianti • Aim: Knowledge-focused

    Last updated Jun 27, 2026 08:02 UTC

Cure My Disease

Helping patients find clinical trials that match their disease.

Why was Cure my disease built?

Explore

Home News Browse About Terms of use Contact us

This is a site from Cyber and Space