Phase 3 Study of EBI-005 in Dry Eye Disease (EBI-005)

June 10, 2015 updated by: Eleven Biotherapeutics

A Multi-Center, Double-Masked, Randomized, Controlled, Efficacy and Safety Study of EBI-005 5 mg/mL Topical Ophthalmic Solution Versus Vehicle Contraol In Subjects With Moderate to Severe Dry Eye Disease

This is a phase III double-masked, randomized, controlled study evaluating the efficacy of EBI-005 as compared to vehicle given as a topical ophthalmic solution in each eye to subjects with moderate to severe DED three times daily for 12 weeks. Approximately 730 subjects at up to approximately 50 centers in the United States will be screened, enrolled into the study.

Study Overview

Status

Status

Indicates the current recruitment status or the expanded access status.
Completed

Conditions

Conditions

The disease, disorder, syndrome, illness, or injury that is being studied. On ClinicalTrials.gov, conditions may also include other health-related issues, such as lifespan, quality of life, and health risks.

Intervention / Treatment

Intervention / Treatment

A process or action that is the focus of a clinical study. Interventions include drugs, medical devices, procedures, vaccines, and other products that are either investigational or already available. Interventions can also include noninvasive approaches, such as education or modifying diet and exercise.

Study Type

Study Type

Describes the nature of a clinical study. Study types include interventional studies (also called clinical trials), observational studies (including patient registries), and expanded access.
Interventional

Enrollment (Actual)

Enrollment

The number of participants in a clinical study. The "anticipated" enrollment is the target number of participants that the researchers need for the study.
670

Phase

Phase

The stage of a clinical trial studying a drug or biological product, based on definitions developed by the U.S. Food and Drug Administration (FDA). The phase is based on the study's objective, the number of participants, and other characteristics. There are five phases: Early Phase 1 (formerly listed as Phase 0), Phase 1, Phase 2, Phase 3, and Phase 4. Not Applicable is used to describe trials without FDA-defined phases, including trials of devices or behavioral interventions.
  • Phase 3

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

  • United States
    • Arizona
      • Chandler, Arizona, United States, 85225
        • Investigational Site
      • Mesa, Arizona, United States, 85208
        • Investigational Site
    • Arkansas
      • Little Rock, Arkansas, United States, 72212
        • Investigational Site
    • California
      • Artesia, California, United States, 90701
        • Investigational Site
      • Mission Hills, California, United States, 91345
        • Investigational Site
      • Petaluma, California, United States, 94954
        • Investigational Site
      • Rancho Cordova, California, United States, 95670
        • Investigational Site
      • San Diego, California, United States, 92115
        • Investiational Site
      • Torrence, California, United States, 90505
        • Investigational Site
    • Colorado
      • Littleton, Colorado, United States, 80120
        • Investigational Site
    • Connecticut
      • Hamden, Connecticut, United States, 06518
        • Investigational Site
    • Florida
      • Plantation, Florida, United States, 33324
        • Investigational Site
    • Georgia
      • Roswell, Georgia, United States, 30076
        • Investigational Site
    • Illinois
      • Bloomingdale, Illinois, United States, 60108
        • Investigational Site
    • Indiana
      • Indianapolis, Indiana, United States, 46260
        • Investigational Site
      • Indianapolis, Indiana, United States, 46290
        • Investigational Site
      • New Albany, Indiana, United States, 47150
        • Investigational Site
    • Kentucky
      • Lexington, Kentucky, United States, 40509
        • Investigational Site
      • Louisville, Kentucky, United States, 40217
        • Investigational Site
      • Louisville, Kentucky, United States, 40206
        • Investigational Site
    • Maine
      • Bangor, Maine, United States, 04401
        • Investigational Site
    • Massachusetts
      • Boston, Massachusetts, United States, 02114
        • Investigational Site
      • Winchester, Massachusetts, United States, 01890
        • Investigational Site
    • Missouri
      • Chesterfield, Missouri, United States, 63017
        • Investigational Site
      • Des Peres, Missouri, United States, 63131
        • Investigational Site
      • Kansas City, Missouri, United States, 64111
        • Investigational Site
      • St. Louis, Missouri, United States, 63131
        • Investigational Site
      • Washington, Missouri, United States, 63090
        • Investigational Site
    • Nevada
      • Las Vegas, Nevada, United States, 89148
        • Investigational Site
    • New York
      • New York, New York, United States, 10036
        • Investigational Site
      • Rochester, New York, United States, 14618
        • Investigational Site
      • Wantagh, New York, United States, 11793
        • Investigational Site
    • North Carolina
      • High Point, North Carolina, United States, 27262
        • Investigational Site
    • Ohio
      • Cleveland, Ohio, United States, 44115
        • Investigational Site
    • Pennsylvania
      • Cranberry Township, Pennsylvania, United States, 16066
        • Investigational Site
      • Lancaster, Pennsylvania, United States, 17601
        • Investigational Site
      • Pittsburgh, Pennsylvania, United States, 15213
        • Investigational Site
    • South Dakota
      • Rapid City, South Dakota, United States, 57701
        • Investigational Site
    • Tennessee
      • Memphis, Tennessee, United States, 38119
        • Investigational Site
    • Texas
      • Houston, Texas, United States, 77034
        • Investigational Site
      • Houston, Texas, United States, 77055
        • Investigational Site#2
      • League City, Texas, United States, 77573
        • Investigational Site
      • San Antonio, Texas, United States, 78209
        • Investigational Site
      • San Antonio, Texas, United States, 78229
        • Investigational Site# 2
    • Virginia
      • Norfolk, Virginia, United States, 23502
        • Investigational Site

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Eligibility Criteria

The key requirements that people who want to participate in a clinical study must meet or the characteristics they must have. Eligibility criteria consist of both inclusion criteria (which are required for a person to participate in the study) and exclusion criteria (which prevent a person from participating). Types of eligibility criteria include whether a study accepts healthy volunteers, has age or age group requirements, or is limited by sex.

Ages Eligible for Study

18 years and older (Adult, Older Adult)

Accepts Healthy Volunteers

No

Genders Eligible for Study

All

Description

Inclusion Criteria:

  • Give written informed consent and any authorizations required by local law (e.g., Protected Health Information waiver) prior to performing any study procedures;
  • Are ≥ 18 years of age;
  • Are willing and able to follow instructions and can be present for the required study visits for the duration of the study;
  • Have a history of dry eye disease (DED) in both eyes supported by a previous clinical diagnosis
  • Have normal lid anatomy.
  • If female and of child bearing potential, she must not be not pregnant or lactating and not sexually active (abstinent) within 14 days prior to Visit 1

Exclusion Criteria:

  • Have signs of infection (i.e., fever or current treatment with antibiotics)
  • Have been exposed to an investigational drug/device within the preceding 30 days
  • Be an employee of the site that is directly involved in the management, administration, or support of the study, or be an immediate family member of the same
  • Be unwilling to or unable to comply with the study

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: Treatment
  • Allocation: Randomized
  • Interventional Model: Parallel Assignment
  • Masking: Triple

Arms and Interventions

Participant Group / Arm

Participant Group / Arm

A group or subgroup of participants in a clinical trial that receives a specific intervention/treatment, or no intervention, according to the trial's protocol.
Intervention / Treatment

Intervention / Treatment

A process or action that is the focus of a clinical study. Interventions include drugs, medical devices, procedures, vaccines, and other products that are either investigational or already available. Interventions can also include noninvasive approaches, such as education or modifying diet and exercise.
Active Comparator: Active Comparator: EBI-005
Drug: EBI-005 The investigational drug EBI-005, is an intervention to one of two study arms: 5 mg/mL topical administered 3 times per day.
Drug: Active Comparator EBI-005
Placebo Comparator: Placebo Comparator
One of two study arms: placebo topical administered 3 times per day.
Drug: Placebo Comparator

What is the study measuring?

Primary Outcome Measures

Primary Outcome Measures

In a clinical study's protocol, the planned outcome measure that is the most important for evaluating the effect of an intervention/treatment. Most clinical studies have one primary outcome measure, but some have more than one.
Outcome Measure
Measure Description
Time Frame
NEI score for Total Corneal Fluorescein Staining (TCFS)
Time Frame: 3 months
To evaluate the efficacy of EBI-005 5 mg/mL topical ophthalmic solution given three times daily for 12 weeks as measured by the change in the NEI score for the Total Corneal Fluorescein Staining [sign] from baseline to Week 12 and a change in ocular pain as measured by the painful or sore eye question on the OSDI [symptom] of DED from baseline to Week 12 as compared to vehicle control.
3 months

Secondary Outcome Measures

Secondary Outcome Measures

In a clinical study's protocol, a planned outcome measure that is not as important as the primary outcome measure for evaluating the effect of an intervention but is still of interest. Most clinical studies have more than one secondary outcome measure.
Outcome Measure
Measure Description
Time Frame
The key secondary endpoint is total OSDI score
Time Frame: 3 months
Change from baseline to week 12 in Total OSDI score.
3 months

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Sponsor

Sponsor

The organization or person who initiates the study and who has authority and control over the study.
Eleven Biotherapeutics

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start

Study Start

The actual date on which the first participant was enrolled in a clinical study. The "anticipated" study start date is the date that the researchers think will be the study start date.
January 1, 2014

Primary Completion (Actual)

Primary Completion

The date on which the last participant in a clinical study was examined or received an intervention to collect final data for the primary outcome measure. Whether the clinical study ended according to the protocol or was terminated does not affect this date. For clinical studies with more than one primary outcome measure with different completion dates, this term refers to the date on which data collection is completed for all the primary outcome measures. The "anticipated" primary completion date is the date that the researchers think will be the primary completion date for the study.
March 1, 2015

Study Completion (Actual)

Study Completion

The date on which the last participant in a clinical study was examined or received an intervention/treatment to collect final data for the primary outcome measures, secondary outcome measures, and adverse events (that is, the last participant's last visit). The "anticipated" study completion date is the date that the researchers think will be the study completion date.
April 1, 2015

Study Registration Dates

First Submitted

First Submitted

The date on which the study sponsor or investigator first submitted a study record to ClinicalTrials.gov. There is typically a delay of a few days between the first submitted date and the record's availability on ClinicalTrials.gov (the first posted date).
November 25, 2013

First Submitted That Met QC Criteria

First Submitted That Met QC Criteria

The date on which the study sponsor or investigator first submits a study record that is consistent with National Library of Medicine (NLM) quality control (QC) review criteria. The sponsor or investigator may need to revise and submit a study record one or more times before NLM's QC review criteria are met. It is the responsibility of the sponsor or investigator to ensure that the study record is consistent with the NLM QC review criteria.
November 25, 2013

First Posted (Estimate)

First Posted

The date on which the study record was first available on ClinicalTrials.gov after National Library of Medicine (NLM) quality control (QC) review has concluded. There is typically a delay of a few days between the date the study sponsor or investigator submitted the study record and the first posted date.
December 2, 2013

Study Record Updates

Last Update Posted (Estimate)

Last Update Posted

The most recent date on which changes to a study record were made available on ClinicalTrials.gov. There may be a delay between when the changes were submitted to ClinicalTrials.gov by the study's sponsor or investigator (the last update submitted date) and the last update posted date.
June 11, 2015

Last Update Submitted That Met QC Criteria

Last Update Submitted That Met QC Criteria

The most recent date on which the study sponsor or investigator submitted changes to a study record that are consistent with National Library of Medicine (NLM) quality control (QC) review criteria. It is the responsibility of the sponsor or investigator to ensure that the study record is consistent with the NLM QC review criteria.
June 10, 2015

Last Verified

Last Verified

The most recent date on which the study sponsor or investigator confirmed the information about a clinical study on ClinicalTrials.gov as accurate and current. If a study with a recruitment status of recruiting; not yet recruiting; or active, not recruiting has not been confirmed within the past 2 years, the study's recruitment status is shown as unknown.
June 1, 2015

More Information

Terms related to this study

Additional Relevant MeSH Terms

Other Study ID Numbers

Other Study ID Numbers

Identifiers or ID numbers other than the NCT number that are assigned to a clinical study by the study's sponsor, funders, or others. These numbers may include unique identifiers from other trial registries and National Institutes of Health grant numbers.
  • EBI-005-3

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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Conditions

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Sponsor/Collaborators

Locations

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