Study of Difluprednate Ophthalmic Emulsion in the Treatment of Uveitis

Status Completed

Clinical Trial Summary

The purpose of this phase 3 confirmatory study is to determine if difluprednate ophthalmic emulsion is effective in the treatment of treatment of uveitis.

Clinical Trial Description

The objective of this phase 3 study is to assess the efficacy and safety of 0.05% difluprednate ophthalmic emulsion (DFBA) in patients with endogenous anterior uveitis, in comparison with 0.1% betamethasone sodium phosphate ophthalmic solution (BP). ;

Study Design

Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double-Blind, Primary Purpose: Treatment

Related Conditions & MeSH terms

Clinical Trial Details

NCT number	NCT00406887
Study type	Interventional
Source	Sirion Therapeutics, Inc.
Contact
Status	Completed
Phase	Phase 3
Start date	August 2002
Completion date	November 2003

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See also
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