New eye drops aim to calm Sjögren's dry eye by blocking inflammation

Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.

Inclusion Criteria: * 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. Exclusion Criteria: * 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.