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Completed Phase 3 Interventional Results available

A Phase 3 Study to Evaluate the Efficacy of Lifitegrast in Subjects With Dry Eye

ClinicalTrials.gov ID: NCT01743729

Public ClinicalTrials.gov record NCT01743729. 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 Jul 22, 2026, 4:50 PM 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 3, Multicenter, Randomized, Double-Masked and Placebo-Controlled Study Evaluating the Efficacy of a 5.0% Concentration of Lifitegrast Ophthalmic Solution Compared to Placebo in Subjects With Dry Eye Currently Using Artificial Tears (OPUS-2)

Study identification

NCT ID
NCT01743729
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
Shire
Industry
Enrollment
720 participants

Conditions and interventions

Interventions

  • Lifitegrast Drug
  • Placebo Drug

Drug

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
Dec 6, 2012
Primary completion
Sep 30, 2013
Completion
Sep 30, 2013
Last update posted
Jun 22, 2021

2012 – 2013

United States locations

U.S. sites
31
U.S. states
13
U.S. cities
28
Facility City State ZIP Site status
OPUS-2 Investigational Site Artesia California 90701
OPUS-2 Investigational Site Hemet California 92545
OPUS-2 Investigational Site Lancaster California 93534
OPUS-2 Investigational Site Mission Hills California 91345
OPUS-2 Investigational Site Montebello California 90640
OPUS-2 Investigational Site Newport Beach California 92663
OPUS-2 Investigational Site Petaluma California 94954
OPUS-2 Investigational SIte Rancho Cordova California 95670
OPUS-2 Investigational Site Danbury Connecticut 06810
OPUS-2 Investigational Site Fort Myers Florida 33901
OPUS-2 Investigational Site Hoffman Estates Illinois 60169
OPUS-2 Investigational Site Indianapolis Indiana 46260
OPUS-2 Investigational Site New Albany Indiana 47150
OPUS-2 Investigational Site Lexington Kentucky 40509
OPUS-2 Investigational Site Saint Paul Minnesota 55082
OPUS-2 Investigational Site Chesterfield Missouri 63017
OPUS-2 Investigational Site Des Peres Missouri 63131
OPUS-2 Investigational Site Independence Missouri 64055
OPUS-2 Investigational Site Kansas City Missouri 64111
OPUS-2 Investigational Site Washington Missouri 63090
OPUS-2 Investigational Site New York New York 10016
OPUS-2 Investigational Site New York New York 10036
OPUS-2 Investigational Site Wantagh New York 11793
OPUS-2 Investigational Site Cleveland Ohio 44115
OPUS-2 Investigational Site Philadelphia Pennsylvania 19148
OPUS-2 Investigational Site Houston Texas 77034
OPUS-2 Investigational Site Houston Texas 77055
OPUS-2 Investigational Site League City Texas 77573
OPUS-2 Investigational Site San Antonio Texas 78209
OPUS-2 Investigational Site San Antonio Texas 78229
OPUS-2 Investigational Site Norfolk Virginia 23502

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 NCT01743729, 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 Jun 22, 2021 · Synced Jul 22, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT01743729 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →