Actively Recruiting

Phase 4
Age: 18Years +
All Genders
NCT07277257

Evaluating a New Therapy for Dry Eye in Patients With Sjögren's Syndrome

Led by Center For Sight · Updated on 2025-12-22

35

Participants Needed

1

Research Sites

56 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

This study will evaluate the effect of TRYPTYR in patients with Sjögren's syndrome-related dry eye disease. The goal is to determine whether TRYPTYR can improve symptoms and signs of dry eye in this specific patient population.

CONDITIONS

Official Title

Evaluating a New Therapy for Dry Eye in Patients With Sjögren's Syndrome

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Adults over 18 years old with dry eye disease caused by Sj�f6gren's syndrome diagnosed within the past 2 years
  • History of using or wanting artificial tears for dry eye symptoms within the past 2 months
  • Unanesthetized Schirmer's Test score of 1 mm or more and less than 10 mm in 5 minutes
  • Baseline total Corneal Fluorescein Staining score between 2 and 15 on the National Eye Institute grading scale
Not Eligible

You will not qualify if you...

  • History of eye surgery within the past 6 months
  • Contact lens use in either eye within 7 days before baseline or during the study
  • Current topical treatment for less than 3 months or expected changes to treatment during the study
  • Use of topical steroid eye medication or varenicline nasal spray within 4 weeks before baseline or during the study
  • Use of artificial tears within 2 hours before baseline or study visits
  • Allergy to any component of the study drug
  • Severe, uncontrolled autoimmune diseases such as rheumatoid arthritis or lupus, especially with severe systemic symptoms

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

Center For Sight

Venice, Florida, United States, 34285

Actively Recruiting

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Research Team

G

Gina Thomas

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

NA

Model

SINGLE_GROUP

Primary Purpose

TREATMENT

Number of Arms

1

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