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Disease · MONDO_0006640

adrenal gland hyperfunction

6 sourcesdiseases-2026-09-18-0.1.0

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ConductScience Library. adrenal gland hyperfunction. Diseases, record MONDO_0006640. Release diseases-2026-09-18-0.1.0, 18 Sept 2026. https://conductscience.org/library/diseases/MONDO_0006640

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Disease

Names and IDs as Open Targets gives them. Its IDs in MeSH, Orphanet, the Disease Ontology and the NCI Thesaurus are those Open Targets states for it.

Name
adrenal gland hyperfunction
Open Targets
Open Targets ID
MONDO_0006640
Open Targets
Other names
Adrenocortical Hyperfunction, Overproduction of cortisol, disorder of corticoadrenal overactivity, hyperadrenalism, hypercortisolemia, hypercortisolism, hypercortisolism (disorder)
Open Targets
Disease Ontology
DOID:3947
Disease Ontology
MeSH
D000308
MeSH
Highest stage of its drugs
Approval, for 2 of its 5 drugs, from DailyMed
Open Targets

Drugs5

The drugs Open Targets' clinical reports study for the disease, the highest stage first, then the most trial reports. The stage is Open Targets', the highest any of its sources reports for the pair, and each row names the sources that report it.

DrugChEMBL IDTypeOpen Targets' stageStage reported byReportsOf them trialsTrials shown hereSource
DEXAMETHASONECHEMBL384467Small moleculeApprovalDailyMed100Drugs and targets
LEVOKETOCONAZOLECHEMBL295698Small moleculeApprovalDailyMed100Drugs and targets
RELACORILANTCHEMBL4068611Small moleculePhase 3ClinicalTrials.gov111Drugs and targets
CLOFUTRIBENCHEMBL5314513Small moleculePhase 2ClinicalTrials.gov111Drugs and targets
METYRAPONECHEMBL934Small moleculeUnknownClinicalTrials.gov111Drugs and targets

Targets5

The targets ChEMBL's mechanism records give for the disease's drugs, through Open Targets, the most drugs first. A mechanism record says what a drug acts on, not that the target causes the disease.

TargetProteinIts drugs that act on itMechanismsHighest stage of those drugsGene in GenesSource
CYP11B1Cytochrome P450 11B1, mitochondrial2Cytochrome P450 11B1 inhibitor; Cytochrome P450 11B1, mitochondrial inhibitorApprovalhttps://conductscience.org/library/genes/1584Drugs and targets
NR3C1Glucocorticoid receptor2Glucocorticoid receptor agonist; Glucocorticoid receptor antagonistApprovalhttps://conductscience.org/library/genes/2908Drugs and targets
CYP11A1Cholesterol side-chain cleavage enzyme, mitochondrial1Cytochrome P450 11A1 inhibitorApprovalhttps://conductscience.org/library/genes/1583Drugs and targets
CYP11B2Cytochrome P450 11B2, mitochondrial1Cytochrome P450 11B2 inhibitorApprovalhttps://conductscience.org/library/genes/1585Drugs and targets
CYP17A1Steroid 17-alpha-hydroxylase/17,20 lyase1Cytochrome P450 17A1 inhibitorApprovalhttps://conductscience.org/library/genes/1586Drugs and targets

Trials3

Trials an Open Targets clinical report links to the disease, posted results first, then the largest. A trial is shown when the release's checks confirm its link to the disease and Drugs and targets shows its link to one of the disease's drugs.

TrialTitlePhaseParticipantsResults first postedConditionsDrugsLinked bySource
NCT04308590A Study of the Efficacy and Safety of Relacorilant in Patients With Cortisol-Secreting Adrenal AdenomasPhase 31372025-08-03HypercortisolismRELACORILANTIts record names the diseaseClinicalTrials.gov
NCT05436639SPI-62 as a Treatment for Hypercortisolism Related to a Benign Adrenal TumorPhase 230Autonomous Cortisol Secretion (ACS), ACTH-Independent Cushing Syndrome, ACTH-Independent Adrenal Cushing Syndrome, SomaticCLOFUTRIBENIts record names the diseaseClinicalTrials.gov
NCT05255900Effects of Metyrapone in Patients With Hypercortisolism20HypercortisolismMETYRAPONEIts record names the diseaseClinicalTrials.gov

Comparisons in its trials12

Comparisons Trial comparisons calculated in the trials shown here, most participants first. A comparison in one of these trials does not always compare a treatment for the disease, so read the two groups.

ComparisonGroup 1, with the outcomeGroup 2, with the outcomeParticipantsTrialSource
Relacorilant vs Placebo: Number of Patients With 1 or More Treatment-emergent Adverse Events (TEAEs) as Graded by CTCAE v5.0.67 of 6860 of 69137NCT04308590Trial comparisons
Relacorilant vs Placebo: deaths from any cause1 of 680 of 69137NCT04308590Trial comparisons
Relacorilant vs Placebo: serious adverse events15 of 684 of 69137NCT04308590Trial comparisons
Relacorilant vs Placebo: Number of Patients With a Reduction in 24-hour Average SBP by ≥5 mm Hg10 of 4213 of 4284NCT04308590Trial comparisons
Relacorilant vs Placebo: Number of Patients With Normalization of the 24-hour Average SBP (<130 mm Hg)9 of 4213 of 4284NCT04308590Trial comparisons
Relacorilant vs Placebo: Number of Patients With Any Dose Decrease in Antihypertensive Medication7 of 225 of 3355NCT04308590Trial comparisons
Relacorilant vs Placebo: Number of Patients With DM Who Achieved 2-hour oGTT Glucose <140 mg/dL1 of 270 of 2855NCT04308590Trial comparisons
Relacorilant vs Placebo: Number of Patients With Any Dose Increase or Switch in Antihypertensive Medication1 of 225 of 3355NCT04308590Trial comparisons
Relacorilant vs Placebo: Number of Patients With Any Dose Decrease in Diabetes Medication0 of 150 of 2540NCT04308590Trial comparisons
Relacorilant vs Placebo: Number of Patients With Any Dose Increase or Switch in Diabetes Medication4 of 153 of 2540NCT04308590Trial comparisons

Papers from its trials0

The papers the trials shown here list on ClinicalTrials.gov as their results (RESULT) or as drawn from them (DERIVED), results first, newest first.

None in this release.

Data dates

The date of each source this release read.

Open Targets
2026-09-18
Open Targets
Drug links and their checks, from Drugs and targets
2026-09-18
Drugs and targets
ClinicalTrials.gov, from Trials
2026-11-12
Trials
Comparisons, from Trial comparisons
2026-03-23
Trial comparisons
PubMed, for the checks
2026-11-06
PubMed
MeSH, for the checks
2026-11-10
MeSH

Sources 6

  • ClinicalTrials.gov's posted results, through CTTI's AACTFreely available. Acknowledgement requested
  • ChEMBL, through Open TargetsCC BY-SA 3.0
  • ClinicalTrials.govNo license stated
  • NLM's MeSHNLM's terms
  • Open TargetsCC0 1.0
  • PubMedNLM's terms
Each source's terms
  • ClinicalTrials.gov's posted results, through CTTI's AACTClinicalTrials.gov data via Aggregate Analysis of ClinicalTrials.gov (AACT), CTTI. CTTI makes its materials freely available and requests acknowledgement. https://aact.ctti-clinicaltrials.org/documentation/299
  • ChEMBL, through Open TargetsCC BY-SA 3.0, for the parts from ChEMBL. Read on 8 Nov 2026 at https://platform-docs.opentargets.org/licence
  • ClinicalTrials.govnone stated
  • NLM's MeSHNLM's
  • Open TargetsCC0 1.0. Open Targets asks that users cite its latest paper: Buniello et al. 2025, Open Targets Platform: facilitating therapeutic hypotheses building in drug discovery, Nucleic Acids Research 53(D1):D1467, PMID 39657122. Read on 8 Nov 2026 at https://platform-docs.opentargets.org/licence
  • PubMedNLM's terms

ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.

For software

Read this disease from software.

The record and each of its lists are JSON, twenty rows a page. No key.

GET https://conductscience.org/api/diseases/v1/MONDO_0006640

GET https://conductscience.org/api/diseases/v1/MONDO_0006640/drugs