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Not listed Phase 2 Interventional

A Study of TL-925 Ophthalmic Emulsion as a Treatment for Dry Eye Disease

ClinicalTrials.gov ID: NCT06225973

Public ClinicalTrials.gov record NCT06225973. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Oct 17, 2026, 12:23 AM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A Phase 2b, Multicenter, Randomized, Double-masked Vehicle-controlled Study to Evaluate the Efficacy and Safety of TL-925 Ophthalmic Emulsion 0.1% in Subjects With Moderate to Severe Dry Eye Disease

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

In this prospective, phase 2b, multicenter, randomized, double-masked, vehicle-controlled, parallel-arm study, approximately 880 subjects with moderate to severe dry eye disease (DED) will be randomly assigned (1:1) to receive either TL-925 or vehicle as topical ophthalmic eye drops administered bilaterally BID. The study will comprise two phases: a two-week screening phase/run-in and a six-week double-masked treatment phase.

Study identification

NCT ID
NCT06225973
Recruitment status
Not listed
Study type
Interventional
Phase
Phase 2
Lead sponsor
Telios Pharma, Inc.
Industry
Enrollment
880 participants

Conditions and interventions

Interventions

Drug · Other

Eligibility (public fields only)

Age range
18 Years and older
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Feb 6, 2024 (Actual)
Primary completion
Dec 2024 (Estimated)
Completion
Dec 2024 (Estimated)
Last update posted
Jul 10, 2024

2024

United States locations

U.S. sites
18
U.S. states
10
U.S. cities
18
Facility City State ZIP Site status
Cornea and Cataract Consultants of Arizona Phoenix Arizona 85032 —
Global Research Management Glendale California 91204 —
Nvision - La Mesa La Mesa California 91942 —
Nvision - Torrance Torrance California 90505 —
Wyse Eyecare Northbrook Illinois 60062 —
Pankratz Eye Columbus Indiana 47203 —
Butchertown Clinical Louisville Kentucky 40206 —
Andover Eye Associates - Andover Andover Massachusetts 01810 —
Andover Eye Associates - Raynham Raynham Massachusetts 02767 —
NEERA - Westborough Westborough Massachusetts 01581 —
NEERA - Woburn Woburn Massachusetts 01801 —
Oculus Research Garner North Carolina 27529 —
Wilmington Eye Leland North Carolina 28451 —
Scott and Christie EyeCare Associates Cranberry Township Pennsylvania 16066 —
Advancing Vision Research Goodlettsville Tennessee 37072 —
Total Eye Care, PA Memphis Tennessee 38119 —
Advancing Vision Research Smyrna Tennessee 37167 —
Piedmont Eye Center Lynchburg Virginia 24502 —

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT06225973, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Jul 10, 2024 · Synced Oct 17, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT06225973 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →