Corneal neovascularization

disease
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Summary

Corneal neovascularization (MONDO:0006713) is a disease with 9 GWAS associations across 4 studies and 24 clinical trials. Top therapeutic interventions include bevacizumab and pazopanib. A subtype of keratitis — broader associated-gene and molecular evidence is on the parent page (see Disease family below).

At a glance

  • GWAS associations: 9
  • Clinical trials: 24

Clinical features

No curated clinical features (Orphanet) for this disease.

Identifiers

Disease identifiers

FieldValue
Canonical namecorneal neovascularization
Mondo IDMONDO:0006713
EFOEFO:1000880
MeSHD016510
DOIDDOID:11382
ICD-10-CMH16.4
ICD-112077068570
SNOMED CT19161004
UMLSC0085109
MedGen43103
MedDRA10011031
Is cancer (heuristic)no

Data availability: 9 GWAS associations (4 studies).

Disease family

This is a subtype of keratitis. 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 › disorder of orbital regioneye disordercorneal disorderkeratitiscorneal neovascularization

Related subtypes (10): macular keratitis, superficial keratitis, photokeratitis, scleroperikeratitis, filamentary keratitis, corneal ulcer, keratoconjunctivitis, deep keratitis, autosomal dominant keratitis, corneal infection

Subtypes (1): deep corneal vascularisation

Genetics & variants

GWAS landscape

9 GWAS associations across 4 studies. Top hits map to 9 distinct genes (as reported by GWAS).

Top associations by p-value

rsIDp-valueGeneRisk alleleOdds ratio
rs7962560654e-14MSI2T3.98
rs1836403723e-13STK11C3.19
rs1846449142e-12PID1G3.44
rs1844211292e-12ADCY2G2.2
rs7454948003e-12IL17REC3.24
rs1855603213e-11TMEM74 - TRHRC3.37
rs1894642664e-11KLF17C2.93
rs9224686894e-11NT5C1B, NT5C1B-RDH14G2.41
rs5710087254e-11PDE1CT3.05

Top studies (by case count)

StudyLead authorYearCasesControlsTitle
GCST90477724Verma A20241,789444,434Diversity and scale: Genetic architecture of 2068 traits in the VA Million Veteran Program.
GCST90477723Verma A2024517119,668Diversity and scale: Genetic architecture of 2068 traits in the VA Million Veteran Program.
GCST90480084Verma A2024517119,668Diversity and scale: Genetic architecture of 2068 traits in the VA Million Veteran Program.
GCST90481926Verma A202422259,037Diversity and scale: Genetic architecture of 2068 traits in the VA Million Veteran Program.

Variant details and genetic-evidence tiers

Tier distribution (top 50 variants)

TierVariants
Tier 1: coding0
Tier 2: splice/UTR0
Tier 3: regulatory0
Tier 4: intronic/intergenic9

MAF distribution

BucketVariants
common (>=0.05)0
low_freq (0.01-0.05)0
rare (<0.01)9
unknown0

Functional consequences

ConsequenceCount
intron_variant7
intergenic_variant2

Top variants

rsIDChrPosAllelesMAFConsequenceGenep-valueTier
rs7962560651757576626T>A,G0intron_variantMSI24e-14Tier 4: intronic/intergenic
rs183640372191217123C>T0intron_variantSTK113e-13Tier 4: intronic/intergenic
rs1846449142228902656G>A,T0intergenic_variantPID12e-12Tier 4: intronic/intergenic
rs18442112957657283G>A0.001intron_variantADCY22e-12Tier 4: intronic/intergenic
rs74549480039904671C>T0intron_variantIL17RE3e-12Tier 4: intronic/intergenic
rs1855603218108800312C>A,T0intergenic_variantTMEM74 - TRHR3e-11Tier 4: intronic/intergenic
rs189464266144125298C>T0.001intron_variantKLF174e-11Tier 4: intronic/intergenic
rs922468689218577635G>A0.001intron_variantNT5C1B, NT5C1B-RDH144e-11Tier 4: intronic/intergenic
rs571008725732080599T>C,G0.001intron_variantPDE1C4e-11Tier 4: intronic/intergenic

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

0 approved, 2 in late-stage (phase 3) trials. Disease-direct ChEMBL indications, not inferred from the associated-gene cohort below.

DrugDevelopment status
BevacizumabPhase 3 (in late-stage trials)
Sodium ChloridePhase 3 (in late-stage trials)

Clinical trials & evidence

Clinical trials

Clinical trials: 24.

Phase distribution (across all retrieved trials)

PhaseTrials
PHASE1/PHASE27
PHASE17
Not specified6
PHASE2/PHASE32
PHASE41
PHASE21

Top trials by phase / activity

NCTPhaseStatusTitle
NCT00797303PHASE4COMPLETEDThe Effect of Bevacizumab on Corneal Neovascularization
NCT04787471PHASE2/PHASE3RECRUITINGCorneal Crosslinking for Treatment of Corneal Neovascularization
NCT00555594PHASE2/PHASE3COMPLETEDProspective Study to Determine the Effect of Subconjunctival Bevacizumab (AVASTIN) in Corneal Neovascularization
NCT07329686PHASE1/PHASE2RECRUITINGClinical Study of Intrastromal Anti-VEGF Injection for Corneal Neovascularization.
NCT00915590PHASE1/PHASE2TERMINATEDTopical IL-1-Ra for Treatment of Corneal Neovascularization
NCT00992849PHASE2UNKNOWNBevacizumab for the Treatment of Corneal Neovascularization
NCT01072357PHASE1/PHASE2COMPLETEDSafety and Efficacy of Bevacizumab in High-Risk Corneal Transplant Survival
NCT01257750PHASE1/PHASE2COMPLETEDTreatment of Corneal Neovascularization With Topical Pazopanib
NCT01996826PHASE1/PHASE2COMPLETEDA Multi-Center Study of the Safety and Efficacy of Bevacizumab in High-Risk Corneal Transplant Survival
NCT02797704PHASE1/PHASE2TERMINATEDSubconjunctival Aflibercept (EYLEA®) for the Treatment of Corneal Neovascularization
NCT05011916PHASE1/PHASE2UNKNOWNThe Safety and Efficacy of KDR2-2 Suspension Eye Drops in the Treatment of Corneal Neovascularization
NCT00559936PHASE1COMPLETEDTopical Avastin for Treatment of Corneal Neovascularization
NCT00681889PHASE1COMPLETEDEffectiveness and Safety of Topical Ranibizumab for Treatment of Corneal Neovascularization (NV)
NCT00769145PHASE1COMPLETEDRanibizumab for the Inhibition of Neovascularization in the Cornea Following Corneal Transplant Surgery
NCT01868360PHASE1TERMINATEDUsing Aflibercept Injection to Treat Blood Vessel Growth Over the Cornea
NCT02042027PHASE1WITHDRAWNSubconjunctival IVIg (Gamunex-C) Injection for Corneal Neovascularization and Inflammatory Conditions
NCT04215393PHASE1UNKNOWNAn Exploratory Clinical Trial Evaluating the Tolerability and Efficacy of KH906 in Patients With Corneal Neovascularization
NCT04620109PHASE1UNKNOWNClinical Evaluation of Safety and Tolerability of KDR2-2 Eye Drops in Healthy Volunteers With Pharmacokinetic Assessment
NCT00004430Not specifiedCOMPLETEDRandomized Study of Photodynamic Therapy Using Dihematoporphyrin in Patients With Corneal Neovascularization
NCT00471406Not specifiedCOMPLETEDPhotodynamic Therapy With Verteporfin for Corneal Neovascularization
NCT00512876Not specifiedCOMPLETEDEffectiveness and Safety of Topical Bevacizumab (Avastin) for Treatment of Corneal Neovascularization
NCT00515684Not specifiedWITHDRAWNCorneal Thinning During Topical Bevacizumab Therapy
NCT05659940Not specifiedUNKNOWNCorrelation Between a Novel Subset of Neutrophil and Corneal Neovascularization.
NCT06412718Not specifiedUNKNOWNValidation of Human Drugs Target of Repurposed Drugs and Novel Therapies

Drugs tested across these trials (top 30)

MoleculeMax phaseTrials referencing
BEVACIZUMAB46
PAZOPANIB41
CHEMBL406876801
CHEMBL417127701
S-ROLIPRAM01