Blepharitis
diseaseOn this page
Also known as eyelid inflammationinflammation of eyelid
Summary
Blepharitis (MONDO:0004785) is a disease (an umbrella term covering 6 Mondo subtypes) with 2 GWAS associations across 18 studies and 52 clinical trials. Top therapeutic interventions include doxycycline anhydrous, loteprednol etabonate, and azithromycin. A subtype of eyelid disorder — broader associated-gene and molecular evidence is on the parent page (see Disease family below).
At a glance
- Umbrella term: 6 Mondo subtypes
- GWAS associations: 2
- Clinical trials: 52
Clinical features
No curated clinical features (Orphanet) for this disease.
Identifiers
Disease identifiers
| Field | Value |
|---|---|
| Canonical name | blepharitis |
| Mondo ID | MONDO:0004785 |
| EFO | EFO:0009536 |
| MeSH | D001762 |
| DOID | DOID:9423 |
| ICD-10-CM | H01.0 |
| NCIT | C112183 |
| SNOMED CT | 41446000 |
| UMLS | C0005741 |
| MedGen | 598 |
| Is cancer (heuristic) | no |
Also known as: eyelid inflammation · inflammation of eyelid
Data availability: 2 GWAS associations (18 studies).
Disease family
This is a subtype of eyelid 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 › disorder of orbital region › eye adnexa disorder › eyelid disorder › blepharitis
Related subtypes (19): eyelid degenerative disorder, blepharophimosis, hypertrichosis of eyelid, hypotrichosis of eyelid, entropion, lagophthalmos, stenosis of lacrimal punctum, stenosis of lacrimal passage, ectropion, eyelid neoplasm, blepharochalasis, eyelid hypopigmentation, telecanthus, cryptophthalmia, epiblepharon, congenital eyelid retraction, herpes zoster with dermatitis of eyelid, eyelid seborrheic keratosis, dermatosis of eyelid
Subtypes (6): parasitic eyelid infestation, squamous blepharitis, noninfectious dermatoses of eyelid, blepharoconjunctivitis, ulcerative blepharitis, hordeolum
Genetics & variants
GWAS landscape
2 GWAS associations across 18 studies. Top hits map to 1 distinct genes (as reported by GWAS).
Top associations by p-value
| rsID | p-value | Gene | Risk allele | Odds ratio |
|---|---|---|---|---|
| rs1805007 | 3e-12 | MC1R | C | 0.09 |
| rs13178063 | 1e-07 | LINC02227 - EBF1 | ? |
Top studies (by case count)
| Study | Lead author | Year | Cases | Controls | Title |
|---|---|---|---|---|---|
| GCST90475888 | Verma A | 2024 | 37,507 | 369,186 | Diversity and scale: Genetic architecture of 2068 traits in the VA Million Veteran Program. |
| GCST90477742 | Verma A | 2024 | 8,636 | 101,547 | Diversity and scale: Genetic architecture of 2068 traits in the VA Million Veteran Program. |
| GCST90481129 | Verma A | 2024 | 8,636 | 101,547 | Diversity and scale: Genetic architecture of 2068 traits in the VA Million Veteran Program. |
| GCST90473377 | UK Biobank Whole-Genome Sequencing Consortium | 2025 | 5,816 | 452,624 | Whole-genome sequencing of 490,640 UK Biobank participants. |
| GCST90477741 | Verma A | 2024 | 3,623 | 51,121 | Diversity and scale: Genetic architecture of 2068 traits in the VA Million Veteran Program. |
| GCST90079867 | Backman JD | 2021 | 2,724 | 377,649 | Exome sequencing and analysis of 454,787 UK Biobank participants. |
| GCST90083853 | Backman JD | 2021 | 2,724 | 377,649 | Exome sequencing and analysis of 454,787 UK Biobank participants. |
| GCST90436007 | Zhou W | 2018 | 2,396 | 399,306 | Efficiently controlling for case-control imbalance and sample relatedness in large-scale genetic association studies. |
| GCST90043792 | Jiang L | 2021 | 2,119 | 454,229 | A generalized linear mixed model association tool for biobank-scale data. |
| GCST90079866 | Backman JD | 2021 | 1,881 | 381,491 | Exome sequencing and analysis of 454,787 UK Biobank participants. |
Variant details and genetic-evidence tiers
Tier distribution (top 50 variants)
| Tier | Variants |
|---|---|
| Tier 1: coding | 1 |
| Tier 2: splice/UTR | 0 |
| Tier 3: regulatory | 0 |
| Tier 4: intronic/intergenic | 1 |
MAF distribution
| Bucket | Variants |
|---|---|
| common (>=0.05) | 2 |
| low_freq (0.01-0.05) | 0 |
| rare (<0.01) | 0 |
| unknown | 0 |
Functional consequences
| Consequence | Count |
|---|---|
| missense_variant | 1 |
| intergenic_variant | 1 |
Top variants
| rsID | Chr | Pos | Alleles | MAF | Consequence | Gene | p-value | Tier |
|---|---|---|---|---|---|---|---|---|
| rs1805007 | 16 | 89919709 | C>A,G,T | 0.082 | missense_variant | MC1R | 3e-12 | Tier 1: coding |
| rs13178063 | 5 | 158663343 | A>G | 0.05 | intergenic_variant | LINC02227 - EBF1 | 1e-07 | Tier 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, 6 in late-stage (phase 3) trials. Disease-direct ChEMBL indications, not inferred from the associated-gene cohort below.
| Drug | Development status |
|---|---|
| Azithromycin | Phase 3 (in late-stage trials) |
| Dexamethasone | Phase 3 (in late-stage trials) |
| Ivermectin | Phase 3 (in late-stage trials) |
| Lotilaner | Phase 3 (in late-stage trials) |
| Metronidazole | Phase 3 (in late-stage trials) |
| Tobramycin | Phase 3 (in late-stage trials) |
Earlier-phase candidates (phase 2, investigational — efficacy not yet established): Fluticasone Propionate, Loteprednol Etabonate, Povidone.
Clinical trials & evidence
Clinical trials
Clinical trials: 52.
Phase distribution (across all retrieved trials)
| Phase | Trials |
|---|---|
| Not specified | 20 |
| PHASE2 | 12 |
| PHASE4 | 9 |
| PHASE3 | 9 |
| PHASE2/PHASE3 | 1 |
| PHASE1 | 1 |
Top trials by phase / activity
| NCT | Phase | Status | Title |
|---|---|---|---|
| NCT00629590 | PHASE4 | COMPLETED | Safety and Efficacy Pilot Study of AzaSite (Azithromycin) in Subjects With Blepharitis |
| NCT00629941 | PHASE4 | COMPLETED | Safety and Efficacy Study of AzaSite® in Subjects With Blepharitis |
| NCT00629980 | PHASE4 | COMPLETED | Safety and Efficacy Pilot Study of AzaSite® (Azithromycin) in Subjects With Blepharitis |
| NCT00656539 | PHASE4 | COMPLETED | Safety and Efficacy Pilot Study of AzaSite® for Four Weeks in Subjects With Blepharitis |
| NCT00803452 | PHASE4 | COMPLETED | Lipids of the Human Tear Film and Their Effect on Tear Stability |
| NCT01357538 | PHASE4 | COMPLETED | Efficacy and Safety of Posiformin 2 % Eye Ointment in the Treatment of Blepharitis |
| NCT01478256 | PHASE4 | COMPLETED | Comparative Study in the Efficacy of Topical Besifloxocin With Erythromycin for the Management of Acute Blepharitis |
| NCT06795165 | PHASE4 | COMPLETED | Study of the Safety and Efficacy of Moxidectin Tablets for the Reduction of Demodex Eyelash Infestation |
| NCT07451678 | PHASE4 | COMPLETED | Treatment of Blepharitis Induced by Demodex Folliculorum Through Eyelid Cleansing With Wipes Containing Topical Chlorhexidine |
| NCT00732446 | PHASE3 | COMPLETED | Safety/Efficacy of Antibiotic Steroid Combination in Treatment of Blepharitis and/or Keratitis and/or Conjunctivitis |
| NCT00796926 | PHASE3 | COMPLETED | Trial to Compare the Efficacy of Systane Ultra and Refresh Drop in the Treatment of Dry Eye in Asian Eyes |
| NCT01028027 | PHASE3 | COMPLETED | Loteprednol and Tobramycin Versus Tobramycin and Dexamethasone, in the Treatment of Blepharokeratoconjunctivitis |
| NCT01102244 | PHASE3 | COMPLETED | A Study to Evaluate the Clinical Efficacy and Safety of Tobradex® ST Compared to Azasite® in the Treatment of Subjects With Moderate to Severe Chronic Blepharitis |
| NCT01408082 | PHASE3 | COMPLETED | Efficacy and Safety Study of a Steroid/Antibiotic Combination Eyedrop to Treat Non-Bacterial Blepharitis |
| NCT02236403 | PHASE3 | COMPLETED | Treatment of Demodex Blepharitis With Ivermectin Gel 0.1% Plus Metronidazole 1% |
| NCT04475432 | PHASE2/PHASE3 | COMPLETED | Safety and Efficacy of TP-03 for the Treatment of Demodex Blepharitis |
| NCT04784091 | PHASE3 | COMPLETED | Trial to Evaluate the Safety and Efficacy of TP-03 for the Treatment of Demodex Blepharitis |
| NCT05629390 | PHASE3 | COMPLETED | Trial to Evaluate the Efficacy and Safety of TP-03, LIBRA Study |
| NCT06400511 | PHASE3 | TERMINATED | A Phase 3 Study to Evaluate the Efficacy and Safety of Pimecrolimus 0.3% Ophthalmic Ointment |
| NCT06720896 | PHASE2 | ACTIVE_NOT_RECRUITING | A Phase 2, Controlled, Double Blind, Randomized and Multicenter Study to Compare Efficacy and Safety of a Novel Topical Therapy (APT-001, Spinosad 1.8%) in Patients With Blepharitis. |
| NCT00560703 | PHASE2 | COMPLETED | Treatment of Patients With Blepharitis and Facial Rosacea |
| NCT00892970 | PHASE2 | COMPLETED | The Effects of Azithromycin Ophthalmic Solution, 1% Versus Placebo in Subjects With Blepharitis During a Two-Week Treatment Period |
| NCT00894530 | PHASE2 | COMPLETED | The Effects of Azithromycin Ophthalmic Solution, 1% Versus Placebo in Subjects With Blepharitis During a Four-Week Treatment Period (P08638) |
| NCT01073150 | PHASE2 | COMPLETED | Tea Tree Oil in the Treatment of Chronic Blepharitis |
| NCT01089608 | PHASE2 | COMPLETED | Efficacy and Safety Assessment of Azyter® Eye Drops (T1225) in Patients With Blepharitis |
| NCT01269658 | PHASE2 | TERMINATED | A Four Week Study of Azithromycin Ophthalmic Solution, 1% Versus Vehicle in Subjects With Blepharitis (P08636) |
| NCT02218489 | PHASE2 | COMPLETED | Safety and Efficacy of KPI-121 in Subjects With Inflammatory Meibomian Gland Disease |
| NCT03926026 | PHASE2 | COMPLETED | Study Evaluating the Safety and Tolerability of NCX 4251 for the Treatment of Acute Exacerbations of Blepharitis |
| NCT04675242 | PHASE2 | COMPLETED | Study Evaluating the Safety and Efficacy of NCX 4251 Ophthalmic Suspension for the Treatment of Blepharitis |
| NCT05454956 | PHASE2 | COMPLETED | Pilot Study Comparing the Safety and Efficacy of Two Dosing Regimens of TP-03 for the Treatment of MGD |
| NCT06054217 | PHASE2 | UNKNOWN | Effect of an Exploratory Vehicle on Meibomian Gland Dysfunction in Patients With Demodex |
| NCT01647217 | PHASE1 | COMPLETED | Demodex Blepharitis Treatment Study |
| NCT04603222 | Not specified | RECRUITING | Evaluation of SUMMIT BRUSH in Treatment of Blepharitis |
| NCT06371300 | Not specified | RECRUITING | Photobiomodulation With REd vs BluE Light (REBEL) |
| NCT07431385 | Not specified | RECRUITING | Performance and Safety of IRIDIUM GARZE in Blepharitis or Blepharconjunctivitis Adjuvant Treatment |
| NCT00008541 | Not specified | COMPLETED | Evaluation and Treatment of Patients With Corneal and External Diseases |
| NCT01115192 | Not specified | COMPLETED | Blephacura Versus Baby Shampoo to Treat Blepharitis |
| NCT01560962 | Not specified | TERMINATED | Efficacy of Over the Counter (OTC) Povidone-Ioldine 5% for Treatment of Acute or Chronic Blepharitis |
| NCT01808560 | Not specified | COMPLETED | Treatment of Meibomian Gland Dysfunction Prior to Cataract Surgery |
| NCT02386774 | Not specified | COMPLETED | Innovative Imaging of the Conjunctiva, Cornea, and Ocular Adnexa |
Drugs tested across these trials (top 30)
| Molecule | Max phase | Trials referencing |
|---|---|---|
| DOXYCYCLINE ANHYDROUS | 4 | 3 |
| LOTEPREDNOL ETABONATE | 4 | 2 |
| AZITHROMYCIN | 4 | 1 |
| ERYTHROMYCIN | 4 | 1 |
| IVERMECTIN | 4 | 1 |
| LOTILANER | 4 | 1 |
| MOXIFLOXACIN | 4 | 1 |
| PIMECROLIMUS | 4 | 1 |
| POVIDONE | 4 | 1 |
| POVIDONE-IODINE | 4 | 1 |
| TOBRAMYCIN | 4 | 1 |
| LOTEPREDNOL | 3 | 1 |
| BIBROCATHOL | 2 | 1 |
| CHEMBL4299381 | 0 | 1 |
| CHEMBL1823688 | 0 | 1 |
| CHEMBL263291 | 0 | 1 |
| CHEMBL4082099 | 0 | 1 |
| CHEMBL4788951 | 0 | 1 |
| CHEMBL5424182 | 0 | 1 |
| TERPINEOL | 0 | 1 |
| VEHICLE | 0 | 1 |