Lifitegrast for Dry Eye

LT
JM
Overseen ByJeremy M Jones, BS
Age: 18+
Sex: Any
Trial Phase: Phase 4
Sponsor: Pittsburgh Research Institute
Must be taking: Xiidra
No Placebo GroupAll trial participants will receive the active study treatment (no placebo)
Prior Safety DataThis treatment has passed at least one previous human trial

What You Need to Know Before You Apply

What is the purpose of this trial?

This trial examines how Lifitegrast, an eye drop, affects proteins in the tears of people with dry eye disease. It aims to determine if Lifitegrast alters specific markers that provide insights into the condition and its treatment. Ideal participants have experienced dry eyes for at least six months and are currently using Xiidra® drops. As a Phase 4 trial, this research seeks to understand how this FDA-approved and effective treatment benefits more patients.

Do I have to stop taking my current medications for the trial?

The trial does not specify if you need to stop taking your current medications, but you cannot use any eye drops other than Lifitegrast within 2 hours of tear fluid collection. It's best to discuss your specific medications with the trial team.

What is the safety track record for Lifitegrast?

Research has shown that Lifitegrast, available as Xiidra® eye drops, is safe to use. Studies have found that most patients tolerate it well, experiencing only minor side effects. For over seven years, people worldwide have used this treatment without any new safety issues. Serious side effects are rare, and very few people discontinue its use because of them. This evidence suggests that Lifitegrast is a safe choice for treating dry eye disease.12345

Why are researchers enthusiastic about this study treatment?

Most treatments for dry eye disease focus on providing lubrication or reducing inflammation. But Lifitegrast, marketed as Xiidra®, works differently by specifically targeting and blocking the interaction of proteins that contribute to inflammation in the eye, which is a key cause of dry eye symptoms. This unique mechanism of action allows Lifitegrast to directly address the inflammation process, potentially offering faster relief and improvement for patients compared to traditional methods. Researchers are excited about Lifitegrast because its targeted approach could lead to more effective and timely symptom management for those struggling with dry eye disease.

What is the effectiveness track record for Lifitegrast in treating dry eye?

Research has shown that Lifitegrast, marketed as Xiidra, effectively treats dry eye disease (DED). In this trial, subjects with DED will receive Xiidra (lifitegrast ophthalmic solution 5.0%). Studies found that after 12 weeks of using Xiidra, patients experienced significant improvement in both the signs and symptoms of DED. Eye dryness and discomfort scores improved by over 60 points on a 100-point scale. Additionally, about two-thirds of patients reported feeling almost or completely better within 1 to 3 months. These results suggest that Lifitegrast can quickly and effectively relieve dry eyes.678910

Who Is on the Research Team?

LT

Leanne T Labriola, DO, MBA

Principal Investigator

Pittsburgh Research Institute

Are You a Good Fit for This Trial?

This trial is for adults (18+) with a history of dry eye in both eyes, who are using Xiidra and meet certain eye test scores. Participants must not be pregnant or breastfeeding, must stop contact lens use during the study, and cannot have recent eye infections, surgeries, or other serious health issues.

Inclusion Criteria

I am currently using Xiidra eye drops.
Willingness to comply with follow-up schedule and required visits
Corneal fluorescein staining score of inferior 1/3rd of cornea ≥ 2
See 7 more

Exclusion Criteria

Pregnancy or lactation
I am not willing to stop wearing contact lenses during the study.
I do not have HIV, hepatitis, immunodeficiency, or a history of organ or bone marrow transplant.
See 10 more

Timeline for a Trial Participant

Screening

Participants are screened for eligibility to participate in the trial

2-4 weeks

Treatment

Participants receive Xiidra® (Lifitegrast Ophthalmic Solution 5.0%) for dry eye disease

12 weeks
Regular visits for treatment and monitoring

Follow-up

Participants are monitored for safety and effectiveness after treatment

4 weeks

What Are the Treatments Tested in This Trial?

Interventions

  • Lifitegrast

Trial Overview

The study tests how Xiidra (Lifitegrast Ophthalmic Solution 5%) affects tear fluid biomarkers in people with dry eye. All participants receive Xiidra; there is no placebo group. The trial observes changes over time at one center.

How Is the Trial Designed?

2

Treatment groups

Experimental Treatment

Active Control

Group I: DED subjects treated with (Xiidra®) lifitegrast ophthalmic solution 5.0%Experimental Treatment1 Intervention
Group II: Non-DED, non-treatment armActive Control1 Intervention

Find a Clinic Near You

Who Is Running the Clinical Trial?

Pittsburgh Research Institute

Lead Sponsor

Bausch & Lomb Incorporated

Industry Sponsor

Trials
263
Recruited
59,400+
Dr. Christina Ackermann profile image

Dr. Christina Ackermann

Bausch & Lomb Incorporated

Chief Medical Officer since 2023

MD from Harvard Medical School

Brent Saunders profile image

Brent Saunders

Bausch & Lomb Incorporated

Chief Executive Officer since 2023

BA from the University of Pittsburgh, JD and MBA from Temple University

Citations

Efficacy of Lifitegrast Ophthalmic Solution, 5.0%, in Patients ...

The results of this post hoc analysis suggest that lifitegrast treatment may be associated with a response in the signs and symptoms of moderate to severe DED.

Bausch + Lomb Announces Publication of Data From a ...

Median VAS scores improved by 61 and 59 points on a 100-point scale for EOD dryness and discomfort, respectively, after 12 weeks of XIIDRA use.

3.

xiidra-ecp.com

xiidra-ecp.com/efficacy/

The Impact of Xiidra® (lifitegrast ophthalmic solution) 5%

The primary outcome was an improvement in the accuracy of preoperative anterior corneal power measurements at predicting postoperative spherical equivalent ...

Lifitegrast in Treatment of Dry Eye Disease—A Practical ... - PMC

Results: The analysis demonstrated positive effects of lifitegrast on subjective and objective parameters of DED in the selected studies.

208073Orig1s000 - accessdata.fda.gov

Clinical studies have shown that after 12 weeks of topical treatment with Xiidra, there can be an improvement in the signs and symptoms of dry ...

208073Orig1s000 - accessdata.fda.gov

This review concludes that based on face validity, these instruments measure the appropriate key symptoms of patient-reported dry eye and ...

7.

xiidra-ecp.com

xiidra-ecp.com/safety/

Side Effects of Xiidra® (lifitegrast ophthalmic solution) 5%

ESTABLISHED SAFETY PROFILE. Xiidra® was well-tolerated in clinical trials, with low discontinuation rates; over 7 years of global use shows no new safety ...

Safety of Lifitegrast Ophthalmic Solution 5.0% in Patients With ...

Lifitegrast ophthalmic solution 5.0% seemed safe and well tolerated in this study, with no unexpected adverse events.

Lifitegrast Shows Long-Term Safety and Efficacy for Dry Eye ...

A 7-year postmarketing analysis of lifitegrast ophthalmic solution 5% (Xiidra) confirms its favorable safety profile with no new safety signals ...

Withdrawal assessment report - Xiidra - EMA

The targeted indication for lifitegrast is treatment of moderate to severe dry eye disease in adults for whom prior use of artificial tears has been ...