Title

Comparative Study of Thymosin Beta 4 Eye Drops vs. Vehicle in the Treatment of Severe Dry Eye
Comparative Study of Thymosin Beta 4 Eye Drops or Vehicle in the Treatment of Patients With Ocular Surface Defects Due to Severe Dry Eye
  • Phase

    Phase 2
  • Study Type

    Interventional
  • Intervention/Treatment

    thymosin beta-4 ...
  • Study Participants

    9
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.
See above
Study Started
Mar 31
2011
Primary Completion
Dec 31
2012
Study Completion
Dec 31
2012
Results Posted
Dec 23
2015
Estimate
Last Update
Dec 23
2015
Estimate

Drug Thymosin Beta 4 eye drops

Patients will be randomized and will receive the same eye drops the Thymosin Beta 4.

  • Other names: Tβ4

Drug Vehicle Control

Patients will be randomized and will receive the same eye drops without the Thymosin Beta 4.

  • Other names: Vehicle

Thymosin Beta 4 eye drops Experimental

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

Vehicle Control Placebo Comparator

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.

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

Summary

Placebo

Thymosin Beta 4

All Events

Event Type Organ System Event Term

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).

Thymosin

Placebo

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.

Thymosin

4.5
units on a scale (Mean)
Standard Deviation: 3.406

Placebo

11.0
units on a scale (Mean)
Standard Deviation: 4.927

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.

Thymosin

45.625
units on a scale (Mean)
Standard Deviation: 17.780

Placebo

67.233
units on a scale (Mean)
Standard Deviation: 15.658

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).

Thymosin

5.55
seconds (Mean)
Standard Deviation: 2.302

Placebo

2.848
seconds (Mean)
Standard Deviation: 1.137

Total

9
Participants

Age, Continuous

57.33
Years (Mean)
Standard Deviation: 11.18

Age, Categorical

Region of Enrollment

Sex: Female, Male

Overall Study

Thymosin

Placebo