Efficacy Study to Evaluate the Effectiveness of 3 Concentrations of SAR 1118 in Allergic Conjunctivitis
Completed
Shire
Phase 2
2009-04-24
The purpose of this study is to determine whether SAR 1118 at three different concentrations,
compared to placebo, is effective in the prevention of the signs and symptoms of allergic
conjunctivitis
A Study Evaluating the Efficacy of SAR 1118 (0.1%, 1.0%, 5.0%) Ophthalmic Solution in Subjects With Dry Eye Conducted in a Controlled Adverse Environment (CAE)
Completed
Shire
Phase 2
2009-08-03
The purpose of this study is to evaluate the efficacy of three different concentrations
(0.1%, 1.0%, 5.0%) of SAR 1118 Ophthalmic Solution compared to placebo in the treatment of
dry eye.
Safety and Efficacy Study of SAR 1118 to Treat Dry Eye Conducted in a Controlled Adverse Environment (CAE) (OPUS-1)
Completed
Shire
Phase 3
2011-08-29
The purpose of the study is to evaluate the efficacy of SAR 1118 Ophthalmic Solution (5.0%)
compared to placebo in the treatment of Dry Eye. The safety and tolerability of SAR 1118
Ophthalmic Solution (5.0%) compared to placebo in subjects with dry eye when administered BID
for 12 weeks will also be evaluated.
The purpose of the study is to evaluate the safety of lifitegrast ophthalmic solution
compared to placebo in the treatment of dry eye as assessed by ocular and non-ocular adverse
events when administered BID for approximately 1 year.
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