ConductScience.org, home

Disease · MONDO_0006846

malignant hypertension

6 sourcesdiseases-2026-09-18-0.1.0

Download JSON
Cite this record

ConductScience Library. malignant hypertension. Diseases, record MONDO_0006846. Release diseases-2026-09-18-0.1.0, 18 Sept 2026. https://conductscience.org/library/diseases/MONDO_0006846

On this page

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
malignant hypertension
Open Targets
Open Targets ID
MONDO_0006846
Open Targets
Other names
Hypertension, Malignant, accelerated-malignant hypertension, hypertensive emergency, malignant phase hypertension
Open Targets
Disease Ontology
DOID:10824
Disease Ontology
MeSH
D006974
MeSH
Highest stage of its drugs
Approval, for 1 of its 9 drugs, from TTD
Open Targets

Drugs9

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
TRIMETHAPHANCHEMBL1201329Small moleculeApprovalTTD100Drugs and targets
CLEVIDIPINECHEMBL1237132Small moleculePhase 3ClinicalTrials.gov441Drugs and targets
ECULIZUMABCHEMBL1201828AntibodyPhase 3ClinicalTrials.gov111Drugs and targets
NICARDIPINE HYDROCHLORIDECHEMBL1200326Small moleculePhase 3ClinicalTrials.gov111Drugs and targets
TONLAMARSENCHEMBL5095350OligonucleotidePhase 2ClinicalTrials.gov111Drugs and targets
ESMOLOLCHEMBL768Small moleculePhase 1ClinicalTrials.gov111Drugs and targets
LIDOCAINE HYDROCHLORIDECHEMBL1200409Small moleculePhase 1ClinicalTrials.gov111Drugs and targets
MAGNESIUM SULFATECHEMBL3989857Small moleculePhase 1ClinicalTrials.gov111Drugs and targets
NICARDIPINECHEMBL1484Small moleculePhase 1ClinicalTrials.gov111Drugs and targets

Targets19

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
CACNA1CVoltage-gated L-type calcium channel3Voltage-gated L-type calcium channel blockerPhase 3https://conductscience.org/library/genes/775Drugs and targets
CACNA1DVoltage-gated L-type calcium channel3Voltage-gated L-type calcium channel blockerPhase 3https://conductscience.org/library/genes/776Drugs and targets
CACNA1FVoltage-gated L-type calcium channel3Voltage-gated L-type calcium channel blockerPhase 3https://conductscience.org/library/genes/778Drugs and targets
CACNA1SVoltage-gated L-type calcium channel3Voltage-gated L-type calcium channel blockerPhase 3https://conductscience.org/library/genes/779Drugs and targets
ADRB1Beta-1 adrenergic receptor1Beta-1 adrenergic receptor antagonistPhase 1https://conductscience.org/library/genes/153Drugs and targets
ADRB2Beta-2 adrenergic receptor1Beta-2 adrenergic receptor antagonistPhase 1https://conductscience.org/library/genes/154Drugs and targets
C5Complement C51Complement C5 inhibitorPhase 3https://conductscience.org/library/genes/727Drugs and targets
CHRNA3Neuronal acetylcholine receptor; alpha3/beta41Neuronal acetylcholine receptor; alpha3/beta4 antagonistApprovalhttps://conductscience.org/library/genes/1136Drugs and targets
CHRNB4Neuronal acetylcholine receptor; alpha3/beta41Neuronal acetylcholine receptor; alpha3/beta4 antagonistApprovalhttps://conductscience.org/library/genes/1143Drugs and targets
SCN10ASodium channel alpha subunit1Sodium channel alpha subunit blockerPhase 1https://conductscience.org/library/genes/6336Drugs and targets

1 to 10 of 19

See all 19 targets

Trials5

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. 3 more are not shown, since the checks do not confirm them.

TrialTitlePhaseParticipantsResults first postedConditionsDrugsLinked bySource
NCT01951950Nicardipine vs Esmolol Craniotomy EmergencePhase 1402014-08-29Brain TumorsESMOLOL, NICARDIPINEOpen Targets' reading of its recordClinicalTrials.gov
NCT04670809Safety and Efficacy Study of Clevidipine Butyrate Injection in Hypertensive EmergenciesPhase 3262Hypertensive EmergencyCLEVIDIPINE, NICARDIPINE HYDROCHLORIDEIts record names the diseaseClinicalTrials.gov
NCT07511361Study of Efficacy and Safety of Tonlamarsen in Participants With a Recent Hospitalization and a Concurrent Episode of Acute Severe HypertensionPhase 2140Hypertension, Acute Severe Hypertension, Hypertensive Emergency, Hypertensive UrgencyTONLAMARSENIts record names the diseaseClinicalTrials.gov
NCT03566329Magnesium Sulphate Versus Lidocaine for Control of Emergence HypertensionPhase 190Craniotomy, HypertensionLIDOCAINE HYDROCHLORIDE, MAGNESIUM SULFATEOpen Targets' reading of its recordClinicalTrials.gov
NCT05726916Eculizumab in Hypertensive Emergency-associated Hemolytic Uremic SyndromePhase 366Hypertensive Emergency-associated Hemolytic Uremic SyndromeECULIZUMABIts record names the diseaseClinicalTrials.gov

Comparisons in its trials2

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
Nicardipine vs Esmolol: serious adverse events0 of 260 of 2652NCT01951950Trial comparisons
Nicardipine vs Esmolol: Failure of Drug to Control Systolic Blood Pressure (SBP) < 140 mmHg1 of 2011 of 2040NCT01951950Trial comparisons

Papers from its trials1

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

PMIDListed asTrials listing it
41231022DERIVED1

Source PubMed

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_0006846

GET https://conductscience.org/api/diseases/v1/MONDO_0006846/drugs