Study of ST266 Eye Drops in Treating Dry Eye

Completed · Phase 1

Conditions studied: Dry Eye Syndrome

In brief

Subjects with moderate-to-severe Dry Eye by symptoms will be screened including history, ophthalmic examination to include the status of their ocular structure and function and evaluation of tear production. Blood will be blood drawn for complete blood count and chemistry panel. They will also have a urinalysis and pregnancy test in women of child-bearing potential. Subjects will have a two week "run-in" period in which they use artificial tears. If their Dry Eye signs and symptoms do not improve significantly, they will be enrolled and will receive study drug. Safety evaluation includes assessment of the structure and function of the eyes including retina examination and corrected visual acuity. Subjects who meet the inclusion and exclusion criteria will be randomly assigned to one of two treatment arms, ST266 or "artificial tears" eye drops. The randomization scheme is 1:1 ST266:artificial tears. Subjects will self-administer their eye drops four times each day. Subjects will be seen in the office of the ophthalmologist/optometrist at baseline (week zero), one week, three weeks, six weeks and ten weeks. Eye examination will be done at each visit. The baseline eye tests and lab work will be repeated after the treatment phase of the study at the end of week six. Following 6 weeks of treatment, the subjects will be followed for 4 additional weeks.

Key facts

Study ID

NCT02369861

Run by

Noveome Biotherapeutics, formerly Stemnion

People needed

30

Starts

2015-03-01

Expected to finish

2015-12-01

Last updated by the study team

2019-05-13

Who can join

Age: 18 and older. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Subjects ages 18 years and older.
• Subjects with symptoms and signs of Dry Eye for > four months supported by previous clinical diagnosis or self-reported history.
• Visual acuity corrected 20/40 or better in each eye.
• If wearing contact lenses, subjects must be willing to refrain from wearing the contact lenses during the study (including washout period).
• Score of 25-75 on the Ocular Surface Disorder Index (OSDI) questionnaire.
• Corneal staining of grade 2 or more anywhere on the cornea (scale 0-4).

You may not qualify if…

• Pregnant or breast feeding.
• Anterior segment disease other than Dry Eye which in the opinion of the investigator would confound the study.
• Macular and neovascular eye diseases
• History of corneal surgery or LASIK (laser in situ keratomileusis) surgery in either eye within the past year.
• Use of cyclosporine, steroid eye drops, serum eye drops, or any other eye medication (except for artificial tears) or experimental drug within the past 30 days.
• Subjects with glaucoma or in whom glaucoma is suspected.
• Use of anticholinergic drugs, antihistamines, beta-blockers, or tricyclic anti-depressants within the past 30 days.
• Asymmetric punctal plugs or punctal cauterization within the past three months.
• History of Stevens-Johnson disease, ocular cicatricial pemphigoid, alkali burn of the eye, or graft-versus-host disease.
• Immune compromise for any reason.
• Kidney or liver function studies >2x the upper limit of normal.
• Symptomatic abnormalities od the lid.
• History of cancer within the past 5 years

Where it is running

• Price Vision Group — Indianapolis, Indiana, United States

Full record on ClinicalTrials.gov

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