Adrenogenital syndrome

disease
On this page

Also known as adrenogenital disorderandrogenital syndromecongenital adrenal hyperplasia

Summary

Adrenogenital syndrome (MONDO:0015898) is a disease and 70 clinical trials. Top therapeutic interventions include crinecerfont, fludrocortisone acetate, and hydrocortisone. A subtype of adrenal gland disorder — broader associated-gene and molecular evidence is on the parent page (see Disease family below).

At a glance

  • Clinical trials: 70

Clinical features

No curated clinical features (Orphanet) for this disease.

Identifiers

Disease identifiers

FieldValue
Canonical nameadrenogenital syndrome
Mondo IDMONDO:0015898
MeSHD047808
Orphanet181412
ICD-11131153029
SNOMED CT267395000
UMLSC0302280
MedGen86215
GARD0020226
MedDRA10061630
Is cancer (heuristic)no

Also known as: adrenogenital disorder · adrenogenital syndrome · androgenital syndrome · congenital adrenal hyperplasia

Disease family

This is a subtype of adrenal gland disorder. Genetic, therapeutic, and trial evidence is largely curated at the broader-term level — see the parent page for the associated-gene cohort and molecular evidence.

Classification path: disease › human disease › disease by body system or component › endocrine system disorderadrenal gland disorderadrenogenital syndrome

Related subtypes (17): medulloadrenal hyperfunction, adrenal cortex disorder, adrenal medullary hyperplasia, pituitary dwarfism, pseudoleprechaunism syndrome, Patterson type, apparent mineralocorticoid excess, autoimmune polyendocrine syndrome type 1, adrenomyodystrophy, corticosteroid-binding globulin deficiency, Congenital adrenal insufficiency with 46, XY sex reversal OR 46,XY disorder of sex development-adrenal insufficiency due to CYP11A1 deficiency, hypoaldosteronism disease, primary pigmented nodular adrenocortical disease, adrenoleukodystrophy, adrenal gland neoplasm, ectopic ACTH secretion syndrome, endogenous Cushing syndrome, isolated micronodular adrenocortical disease

Subtypes (4): cortisone reductase deficiency, glucocorticoid resistance, congenital adrenal hyperplasia, acquired adrenogenital syndrome

Genetics & variants

GWAS landscape

No GWAS associations recorded — common-variant (GWAS) studies don’t cover this disease (typical for Mendelian / rare diseases). See the curated gene cohort and Mendelian overlap below.

Variant details and genetic-evidence tiers

No tiered GWAS variants or ClinVar records for this disease.

Genes & proteins

No associated-gene cohort resolved for this disease. Atlas builds the molecular and therapeutic sections — associated genes, protein families, druggability, pathways, interactions, and drug associations — by aggregating over a disease’s associated genes (resolved via GWAS / GenCC / ClinVar / CIViC), and none resolved here. This is expected for antibody-mediated, autoimmune, or otherwise non-gene-defined conditions; the curated evidence for this disease is its clinical features, GWAS susceptibility, and clinical trials (above).

Function

No pathway enrichment — requires an associated-gene cohort.

Therapeutics

Drugs indicated for this disease

1 approved. Disease-direct ChEMBL indications, not inferred from the associated-gene cohort below.

DrugDevelopment status
Fludrocortisone AcetateApproved (phase 4)

Clinical trials & evidence

Clinical trials

Clinical trials: 70.

Phase distribution (across all retrieved trials)

PhaseTrials
Not specified34
PHASE214
PHASE39
PHASE15
PHASE1/PHASE24
PHASE42
PHASE2/PHASE32

Top trials by phase / activity

NCTPhaseStatusTitle
NCT03760835PHASE4RECRUITINGCongenital Adrenal Hyperplasia Once Daily Hydrocortisone Treatment
NCT04536662PHASE4UNKNOWNComparisons of Different Forms of Glucocorticoid on the Recovery of Reproductive Function in Patients With 21α-hydroxylase Deficiency
NCT04490915PHASE3ACTIVE_NOT_RECRUITINGGlobal Safety and Efficacy Registration Study of Crinecerfont for Congenital Adrenal Hyperplasia
NCT04806451PHASE3ACTIVE_NOT_RECRUITINGGlobal Safety and Efficacy Registration Study of Crinecerfont in Pediatric Participants With Classic Congenital Adrenal Hyperplasia (CAHtalyst Pediatric Study)
NCT07144163PHASE3RECRUITINGA Study to Evaluate Atumelnant in Adults With Congenital Adrenal Hyperplasia
NCT07159841PHASE2/PHASE3RECRUITINGA Study in Pediatric Participants With Congenital Adrenal Hyperplasia (Balance-CAH)
NCT00001521PHASE3COMPLETEDThree Drug Combination Therapy Versus Conventional Treatment of Children With Congenital Adrenal Hyperplasia
NCT02552251PHASE2/PHASE3UNKNOWNCOrticosteroid in Congenital Adrenal Hyperplasia
NCT02716818PHASE3COMPLETEDComparison of Chronocort® With Standard Glucocorticoid Therapy in Patients With Congenital Adrenal Hyperplasia
NCT03062280PHASE3COMPLETEDA Study of the Efficacy, Safety and Tolerability of Chronocort in Treating CAH
NCT03532022PHASE3WITHDRAWNOpen-label Comparison of Chronocort® Versus Standard Glucocorticoid Replacement Therapy
NCT05063994PHASE3COMPLETEDComparison of Chronocort Versus Standard Hydrocortisone Replacement Therapy in Participants Aged 16 Years and Over With Congenital Adrenal Hyperplasia
NCT05299554PHASE3COMPLETEDLong-term Safety Study of Chronocort in the Treatment of Participants With Congenital Adrenal Hyperplasia
NCT04783181PHASE1/PHASE2ACTIVE_NOT_RECRUITINGA Study of Gene Therapy for Classic Congenital Adrenal Hyperplasia (CAH)
NCT05669950PHASE1/PHASE2RECRUITINGA Trial of Lu AG13909 in Participants With Congenital Adrenal Hyperplasia
NCT06712823PHASE2RECRUITINGAn Extension Study to Evaluate Safety and Efficacy in Participants Treated With CRN04894
NCT07187375PHASE2RECRUITINGPharmacokinetics, Safety and Tolerability of Crinecerfont in Participants With Congenital Adrenal Hyperplasia Who Are Less Than 2 Years Old
NCT07536269PHASE2NOT_YET_RECRUITINGSafety, Tolerability, Pharmacokinetics and Pharmacodynamics of Crinecerfont in Participants With Classic Congenital Adrenal Hyperplasia (CAH) Who Are Less Than 4 Years Old
NCT00000102PHASE1/PHASE2COMPLETEDCongenital Adrenal Hyperplasia: Calcium Channels as Therapeutic Targets
NCT00519818PHASE1/PHASE2COMPLETEDComparison of Two Forms of Hydrocortisone in Patients With Congenital Adrenal Hyperplasia
NCT01735617PHASE2COMPLETEDPilot Study to Characterize and Examine the Pharmacokinetics and Efficacy of Chronocort® in Adults With CAH
NCT01859312PHASE2COMPLETEDComparison of Cortisol Pump With Standard Treatment for Congenital Adrenal Hyperplasia
NCT02804178PHASE2COMPLETEDA Study of ATR-101 for the Treatment of Congenital Adrenal Hyperplasia
NCT03257462PHASE2COMPLETEDStudy of SPR001 in Adults With Classic Congenital Adrenal Hyperplasia
NCT03548246PHASE2WITHDRAWNAndrogen Reduction in Congenital Adrenal Hyperplasia
NCT03669549PHASE2TERMINATEDNevanimibe HCl for the Treatment of Classic CAH
NCT03687242PHASE2COMPLETEDStudy to Evaluate the Safety and Efficacy of SPR001 in Subjects With Classic Congenital Adrenal Hyperplasia
NCT04457336PHASE2TERMINATEDA Ph2b to Evaluate Clinical Efficacy and Safety of Tildacerfont in Adult CAH
NCT04544410PHASE2TERMINATEDA Ph2b to Evaluate Tildacerfont in the Reduction of Glucocorticoid Steroid Doses in Adult CAH
NCT05128942PHASE2TERMINATEDA Phase 2 Study to Evaluate the Safety, Efficacy and PK of Tildacerfont in Children Aged 2-17 Years With CAH
NCT05907291PHASE2COMPLETEDEvaluate the Safety, Efficacy, and Pharmacokinetics of CRN04894 in Participants With Congenital Adrenal Hyperplasia (TouCAHn)
NCT02349503PHASE1WITHDRAWNSafety, Pharmacokinetics and Pharmacodynamics of NBI-77860 in Adolescent Females With Congenital Adrenal Hyperplasia
NCT02574910PHASE1TERMINATEDAndrogen Reduction in Congenital Adrenal Hyperplasia, Phase 1
NCT03019614PHASE1COMPLETEDAn Open Label Study in Healthy Volunteers to Compare Chronocort® to Hydrocortisone
NCT03051893PHASE1COMPLETEDA Two-part, Study to Compare the Pharmacokinetics and Dose Proportionality of up to 6 Chronocort Formulations
NCT03718234PHASE1COMPLETEDSubcutaneous Hydrocortisone Children With Congenital Adrenal Hyperplasia
NCT00250159Not specifiedRECRUITINGNatural History Study of Patients With Excess Androgen
NCT04252001Not specifiedNOT_YET_RECRUITINGGrowing up With the Young Endocrine Support System (YESS!)
NCT04463316Not specifiedRECRUITINGGROWing Up With Rare GENEtic Syndromes
NCT06564220Not specifiedNOT_YET_RECRUITINGTesticular Adrenal Rest Tumor in Congenital Adrenal Hyperplasia Patients Attending Assuit University Children Hospital

Drugs tested across these trials (top 30)

MoleculeMax phaseTrials referencing
CRINECERFONT44
FLUDROCORTISONE ACETATE42
HYDROCORTISONE42
HYDROCORTISONE CYPIONATE42
CORTISONE ACETATE41
FLUTAMIDE41
LETROZOLE41
NIFEDIPINE41
PREDNISOLONE41
PREDNISONE41
TESTOLACTONE41
TILDACERFONT25
ATUMELNANT24
NEVANIMIBE23
FLUDROCORTISONE22
VERUCERFONT21
CHEMBL474045202
CHEMBL1572001
CHEMBL16683901
CHEMBL475930701