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Comparative Study of Thymosin Beta 4 Eye Drops vs. Vehicle in the Treatment of Severe Dry Eye

Primary Purpose

Dry Eye, Sjogren's Syndrome, Graft vs. Host Disease

Status
Completed
Phase
Phase 2
Locations
United States
Study Type
Interventional
Intervention
Thymosin Beta 4 eye drops
Vehicle Control
Sponsored by
Michigan Cornea Consultants, PC
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Dry Eye focused on measuring Dry Eye, Sjogren's Syndrome, Graft vs. Host Disease, Rheumatoid arthritis, Systemic lupus erythematosus, Scleroderma

Eligibility Criteria

18 Years - 90 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Schirmers of < 5 mm at 5 minutes
  • TFBUT: less than 10 seconds
  • Corneal staining of >3 of 15: conjunctival staining of >3 of 18
  • Ocular Surface Disease Index of > 50
  • Presumed best corrected vision of 20/60 or better

Exclusion Criteria:

  • Acute or inflammatory corneal disease
  • Pregnancy or lactation
  • Monocular status
  • Punctal occlusion within 30 days
  • Ocular surgery within 3 months
  • Corneal thinning of >50%
  • Active corneal infection
  • History of ocular malignancy
  • Retinal neovascularization
  • Current use of topical cyclosporin A

Sites / Locations

  • Michigan Cornea Consultants, P.C.

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Placebo Comparator

Arm Label

Thymosin Beta 4 eye drops

Vehicle Control

Arm Description

It is a preservative-free, sterile eye drop solution containing Tβ4 for direct instillation into each eye, six times daily for 28 days

It is composed of the same excipients as RGN-259 but does not contain Tβ4 for direct instillation into each eye, six times daily for 28 days.

Outcomes

Primary Outcome Measures

Safety
Sum of adverse events observed at Day 1, Day 14, Day 28 and Day 56. Measurable by Intra-ocular pressure (IOP) by applanation tonometry, Complete ophthalmologic evaluation including fundoscopy, An adverse event (baseline and all subsequent study visits).

Secondary Outcome Measures

Corneal Fluorescein Staining
Ocular surface irregularity as measured by Slit Lamp Examination (SLE) with fluorescein dye staining of the cornea at days 56 (+28 day follow up). The scale used to determine the difference in corneal fluorescein staining is the Oxford scale. (The Oxford Scale measures corneal fluorescein staining) Corneal staining type was assessed by the investigator for each of 5 regions of the cornea, i.e., four quadrants plus central. The five regions were summed, for a maximum score of 25. A higher score represents greater disability.
Ocular Discomfort Index
Dry eye causes ocular discomfort, which is measured using a Ocular Surface Disease Index at 56 day (+28 day followup). (Symptomatic improvement using the validated Ocular Surface Disease Index (OSDI). The OSDI is a questionnaire that consists of 12 questions about ocular irritation and the effect of dry eye on vision. For every question, participants check a score between 0 and 4, where 0 equals "none of the time" and 4 equals "all of the time. OSDI scores are calculated according to: OSDI = [(sum of scores for all questions answered)*100] / [(total number of questions answered)*4]. The OSDI is scored on a scale of 0 to 100, with higher scores representing greater disability.
Tear Film Break up Time
Tear film break up time (TFBUT) was measured to evaluating the quality of tear at 56 day (+28 day follow up). The tear film break-up time is defined as the interval between the last complete blink and the first appearance of a dry spot, or disruption in the tear film. Range : >10 seconds is thought to be normal, <5 seconds low (with high likelihood of dry eye symptoms).

Full Information

First Posted
July 7, 2011
Last Updated
December 21, 2015
Sponsor
Michigan Cornea Consultants, PC
Collaborators
Kresge Eye Institute
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1. Study Identification

Unique Protocol Identification Number
NCT01393132
Brief Title
Comparative Study of Thymosin Beta 4 Eye Drops vs. Vehicle in the Treatment of Severe Dry Eye
Official Title
Comparative Study of Thymosin Beta 4 Eye Drops or Vehicle in the Treatment of Patients With Ocular Surface Defects Due to Severe Dry Eye
Study Type
Interventional

2. Study Status

Record Verification Date
December 2015
Overall Recruitment Status
Completed
Study Start Date
March 2011 (undefined)
Primary Completion Date
December 2012 (Actual)
Study Completion Date
December 2012 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Michigan Cornea Consultants, PC
Collaborators
Kresge Eye Institute

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
Severe dry eye is a debilitating ocular disease resulting in loss of vision, reduced day-to-day function and significant discomfort. Tear substitutes are an important part of the treatment of all patients, however, even with aggressive us, the corneal(ocular)surface often remains very irregular due to poor surface healing. The agent being evaluated in this study, Thymosin Beta 4, promotes healing of the corneal surface and has been studied in patients with recalcitrant corneal ulcers and erosions with significant success (Arch Ophthalmol. 2010;128(5):636-638., Ann of the NY Acad of Sci, May, 2010). The study hypothesis is that Thymosin Beta 4, in its role as a modulator of corneal surface healing, may be able to promote healing of the corneal surface allowing for more conventional modalities to take over and maintain a smooth and regular ocular surface. The investigators hope to be able to demonstrate an improvement in visual acuity, surface healing and a reduction in dry-eye related symptoms.
Detailed Description
See above

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Dry Eye, Sjogren's Syndrome, Graft vs. Host Disease
Keywords
Dry Eye, Sjogren's Syndrome, Graft vs. Host Disease, Rheumatoid arthritis, Systemic lupus erythematosus, Scleroderma

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 2
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigator
Allocation
Randomized
Enrollment
9 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Thymosin Beta 4 eye drops
Arm Type
Experimental
Arm Description
It is a preservative-free, sterile eye drop solution containing Tβ4 for direct instillation into each eye, six times daily for 28 days
Arm Title
Vehicle Control
Arm Type
Placebo Comparator
Arm Description
It is composed of the same excipients as RGN-259 but does not contain Tβ4 for direct instillation into each eye, six times daily for 28 days.
Intervention Type
Drug
Intervention Name(s)
Thymosin Beta 4 eye drops
Other Intervention Name(s)
Tβ4
Intervention Description
Patients will be randomized and will receive the same eye drops the Thymosin Beta 4.
Intervention Type
Drug
Intervention Name(s)
Vehicle Control
Other Intervention Name(s)
Vehicle
Intervention Description
Patients will be randomized and will receive the same eye drops without the Thymosin Beta 4.
Primary Outcome Measure Information:
Title
Safety
Description
Sum of adverse events observed at Day 1, Day 14, Day 28 and Day 56. Measurable by Intra-ocular pressure (IOP) by applanation tonometry, Complete ophthalmologic evaluation including fundoscopy, An adverse event (baseline and all subsequent study visits).
Time Frame
Day 1, Day 14, Day 28 and Day 56
Secondary Outcome Measure Information:
Title
Corneal Fluorescein Staining
Description
Ocular surface irregularity as measured by Slit Lamp Examination (SLE) with fluorescein dye staining of the cornea at days 56 (+28 day follow up). The scale used to determine the difference in corneal fluorescein staining is the Oxford scale. (The Oxford Scale measures corneal fluorescein staining) Corneal staining type was assessed by the investigator for each of 5 regions of the cornea, i.e., four quadrants plus central. The five regions were summed, for a maximum score of 25. A higher score represents greater disability.
Time Frame
Days 56 (+28 day follow up)
Title
Ocular Discomfort Index
Description
Dry eye causes ocular discomfort, which is measured using a Ocular Surface Disease Index at 56 day (+28 day followup). (Symptomatic improvement using the validated Ocular Surface Disease Index (OSDI). The OSDI is a questionnaire that consists of 12 questions about ocular irritation and the effect of dry eye on vision. For every question, participants check a score between 0 and 4, where 0 equals "none of the time" and 4 equals "all of the time. OSDI scores are calculated according to: OSDI = [(sum of scores for all questions answered)*100] / [(total number of questions answered)*4]. The OSDI is scored on a scale of 0 to 100, with higher scores representing greater disability.
Time Frame
Days 56 (+28 day follow up)
Title
Tear Film Break up Time
Description
Tear film break up time (TFBUT) was measured to evaluating the quality of tear at 56 day (+28 day follow up). The tear film break-up time is defined as the interval between the last complete blink and the first appearance of a dry spot, or disruption in the tear film. Range : >10 seconds is thought to be normal, <5 seconds low (with high likelihood of dry eye symptoms).
Time Frame
Days 56 (+28 day follow up)

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
90 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Schirmers of < 5 mm at 5 minutes TFBUT: less than 10 seconds Corneal staining of >3 of 15: conjunctival staining of >3 of 18 Ocular Surface Disease Index of > 50 Presumed best corrected vision of 20/60 or better Exclusion Criteria: Acute or inflammatory corneal disease Pregnancy or lactation Monocular status Punctal occlusion within 30 days Ocular surgery within 3 months Corneal thinning of >50% Active corneal infection History of ocular malignancy Retinal neovascularization Current use of topical cyclosporin A
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Steven P Dunn, M.D.
Organizational Affiliation
Michigan Cornea Consultants, P.C.
Official's Role
Principal Investigator
Facility Information:
Facility Name
Michigan Cornea Consultants, P.C.
City
Southfield
State/Province
Michigan
ZIP/Postal Code
48034
Country
United States

12. IPD Sharing Statement

Citations:
PubMed Identifier
25826322
Citation
Sosne G, Dunn SP, Kim C. Thymosin beta4 significantly improves signs and symptoms of severe dry eye in a phase 2 randomized trial. Cornea. 2015 May;34(5):491-6. doi: 10.1097/ICO.0000000000000379.
Results Reference
derived

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Comparative Study of Thymosin Beta 4 Eye Drops vs. Vehicle in the Treatment of Severe Dry Eye

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