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Clinical Trials/NCT00501579
NCT00501579CompletedPhase 3

Study of Difluprednate in the Treatment of Uveitis

Sirion Therapeutics, Inc.1 site in 1 countryStarted: July 16, 2007Last updated:
Conditions
Drugs

Trial Snapshot

Phase
Phase 3
Status
Completed
Locations
1

Study Overview

Brief Summary

The purpose of this study is to determine the safety and efficacy of difluprednate compared with prednisolone acetate in the treatment of endogenous anterior uveitis.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Masking
Double

Eligibility Criteria

Ages
2 Years to — (Child, Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • •Diagnosis of endogenous anterior uveitis in at least 1 eye

Exclusion Criteria

  • •Presence of intermediate uveitis, posterior uveitis or panuveitis
  • •Corneal abrasion
  • •Any confirmed or suspected active viral, bacterial, or fungal keratoconjunctival disease
  • •Allergy to similar drugs, such as other corticosteroids

Investigators

Sponsor Class
Industry

Study Sites (1)

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