Ocular cicatricial pemphigoid

disease
On this page

Also known as cicatricial pemphigoid, ocularOCPocular pemphigoidpemphigoid, ocular cicatricial

Summary

Ocular cicatricial pemphigoid (MONDO:0008109) is a disease and 7 clinical trials. Top therapeutic interventions include riboflavin and rituximab. A subtype of mucous membrane pemphigoid — broader associated-gene and molecular evidence is on the parent page (see Disease family below).

At a glance

  • Clinical trials: 7

Clinical features

No curated clinical features (Orphanet) for this disease.

Identifiers

Disease identifiers

FieldValue
Canonical nameocular cicatricial pemphigoid
Mondo IDMONDO:0008109
EFOEFO:0008610
OMIM164185
Orphanet99922
ICD-11953963439
NCITC84939
SNOMED CT314757003, 34250006
UMLSC1282359
MedGen266181
GARD0008759
MedDRA10067776
Is cancer (heuristic)no

Also known as: cicatricial pemphigoid, ocular · OCP · ocular cicatricial pemphigoid · ocular pemphigoid · pemphigoid, ocular cicatricial

Disease family

This is a subtype of mucous membrane pemphigoid. 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 › integumentary system disorder › skin disorderdermatitis › autoimmune bullous skin disease › mucous membrane pemphigoidocular cicatricial pemphigoid

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

No druggable-target or therapeutic data for this disease’s cohort.

Clinical trials & evidence

Clinical trials

Clinical trials: 7.

Phase distribution (across all retrieved trials)

PhaseTrials
Not specified4
PHASE1/PHASE22
PHASE11

Top trials by phase / activity

NCTPhaseStatusTitle
NCT00584935PHASE1/PHASE2COMPLETEDClinical Trial Evaluating Rituximab in Ocular Cicatricial Pemphigoid
NCT01582880PHASE1/PHASE2COMPLETEDUse of Cross-linked Donor Corneas as Carriers for the Boston Keratoprosthesis
NCT06926478PHASE1NOT_YET_RECRUITINGSubconjunctival Humira for Boston Keratoprosthesis
NCT02149732Not specifiedAVAILABLEClinical Trial on the Effect of Autologous Oral Mucosal Epithelial Sheet Transplantation
NCT03421548Not specifiedWITHDRAWNImplantable Intraocular Pressure Sensor for Glaucoma Monitoring in Patients With Boston Keratoprosthesis Type 1
NCT05347667Not specifiedCOMPLETEDMenstrual Cycle Phase and Oral Contraceptive Pill (OCP) Use on Muscle Protein Synthesis
NCT06412718Not specifiedUNKNOWNValidation of Human Drugs Target of Repurposed Drugs and Novel Therapies

Drugs tested across these trials (top 30)

MoleculeMax phaseTrials referencing
RIBOFLAVIN41
RITUXIMAB41
CHEMBL51156501
CHEMBL526727901