Status:

COMPLETED

Evaluating Safety and Efficacy of FID 112903 Post Discontinuation of Long-term Use of RESTASIS® (Cyclosporine Ophthalmic Emulsion) 0.05%

Lead Sponsor:

Alcon Research

Conditions:

Dry Eye Syndrome

Eligibility:

All Genders

18+ years

Phase:

PHASE4

Brief Summary

The purpose of this study is to evaluate the safety and efficacy of FID 112903 given as an immediate treatment replacement in dry eye subjects that discontinue at least 6 months use of RESTASIS.

Eligibility Criteria

Inclusion

  • Patients must be at least 18 years of age
  • Patients must have a best corrected visual acuity of 0.6 LogMar or better in each eye, and must use Restasis BID for at least 6 months.
  • Lastly, patients must have a sodium fluorescein (NaFl) corneal staining sum score of greater than or equal to 3 in the worse eye.

Exclusion

  • Patients cannot wear contact lenses during the study and cannot have a history of hypersensitivity to any component of FID 112903.
  • Patients cannot have ocular or intraocular surgery or serious ocular trauma within the past 6 months, and cannot have punctal plugs of any type.
  • Patients cannot use any prescription topical medication for other ocular conditions (such as glaucoma, uveitis, etc).
  • Patients cannot use systemic medications that may contribute to dry eye if the dosing regimen has not been stable for at least 30 days prior to Visit 1.
  • Patients cannot have ocular conditions that, in the opinion of the investigator, preclude the safe administration of the test article.
  • Patients cannot have a history and/or current evidence of the following: epithelial herpes simplex keratitis (dendritic keratitis); vaccinia, active or recent varicella viral disease of the cornea and/or conjunctiva; active ocular rosacea; acute or chronic bacterial disease of the cornea and/or conjunctiva and/or eyelids; mycobacterial infection of the eye; and/or fungal diseases of the eye.

Key Trial Info

Start Date :

September 1 2010

Trial Type :

INTERVENTIONAL

Allocation :

ACTUAL

End Date :

May 1 2011

Estimated Enrollment :

48 Patients enrolled

Trial Details

Trial ID

NCT01198782

Start Date

September 1 2010

End Date

May 1 2011

Last Update

November 18 2016

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