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Uveitis

LME-636 (A Phase II Study: To evaluate the efficacy of topical LME636 in reducing ocular inflammation in AAU. To evaluate the safety and tolerability of LME636 administered topically to the eye for up to 21 days in AAU patients.

To read more about this study click here.

For additional information or if you think you may be a candidate for  this trial click here.

Study Coordinator (Marvin Martinez): mmartinez@saeye.com