Last updated 48 days ago

Safety and Efficacy of Topical Infliximab in Autoimmune Dry Eye Disease

38 patients around the world

Available in Mexico

Sjögren's syndrome is a condition in which the immune system attacks the body's moisture-producing glands. This often causes severe dry eye, leading to discomfort, irritation, blurred vision, and damage to the eye surface. Inflammation plays an important role in this process, and a protein called TNF-alpha is one of the key drivers. This study will test a new eye drop containing infliximab, a medication that blocks TNF-alpha. The goal is to see whether this treatment can safely improve symptoms and signs of severe dry eye in patients with Sjögren's syndrome.

Instituto de Oftalmología Fundación Conde de Valenciana

1Research sites

38Patients around the world

This study is for people with

Rare diseases

Sjogren's syndrome

Eye Diseases

Dry eye syndrome

Requirements for the patient

From 18 Years

All Gender

Medical requirements

: Adult patients (≥ 18 years).
Confirmed diagnosis of primary or secondary Sjögren's syndrome according to the 2016 ACR/EULAR classification criteria.
On stable systemic immunomodulatory therapy (non-biologic) for at least 12 weeks, with no planned changes during the study (see section 14.1 if there are concerns about confounding variables).
Negative chest X-ray or Interferon-Gamma Release Assays (IGRA).
Diagnosis of severe dry eye, defined by meeting all of the following criteria in at least one eye at study entry.
OSS (SICCA 0-12) ≥ 6 in at least one eye.
OSDI ≥ 33 (severe symptoms).
Symptoms: OSDI score ≥ 33.
Signs: Ocular Staining Score (OSS, SICCA) ≥ 6.
Ability to understand and sign informed consent and to comply with study procedures and treatment administration.

: Current use of topical corticosteroids or topical immunomodulators (cyclosporine, lifitegrast, tacrolimus, autologous serum) within 30 days prior to enrollment.
Current or recent use (\< 3 months) of punctal plugs.
Active ocular infection (bacterial, viral, fungal) or recent history of herpetic keratitis.
Ocular or eyelid surgery within the past 6 months.
Use of contact lenses during the study period.
Known allergy or hypersensitivity to infliximab, murine proteins, or any component of the formulation (including CMC).
Coexisting ocular conditions that may interfere with dry eye evaluation (e.g., active ocular cicatricial pemphigoid, active ocular graft-versus-host disease, uncontrolled glaucoma, significant corneal dystrophy).
Systemic conditions considered contraindications to infliximab exposure, including: active systemic infection, untreated active or latent tuberculosis, history of demyelinating disease, moderate to severe congestive heart failure (NYHA Class III/IV), or history of malignancy within the past 5 years.
Use of systemic biologic agents within the past 6 months (12 months for systemic anti-TNF-α therapy).
Pregnancy, breastfeeding, or intention to become pregnant during the study.
Participation in another clinical trial with an investigational drug within the past 30 days.
Ability to understand and sign informed consent and to comply with study procedures and treatment administration.

Sites

Instituto de Oftalmología FAP Conde de Valenciana, IAP Sede Centro

Chimalpopoca 14, Obrera, Cuauhtémoc, 06080 Ciudad de México, CDMX, Mexico

StudyINFLIXIDRY

SponsorInstituto de Oftalmología Fundación Conde de Valenciana

Study typeInterventional

Conditions

Sjogren's syndromeDry eye syndrome

Requirements

From 18 YearsAll Gender

Unique study IDclinicaltrials.gov

NCT07671222