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6 Week DEX PS DDS Study

Principal Investigator

C. Michael Samson, MD

Enrollment Status

Completed

Objective

To evaluate the safety and efficacy of the 700 μg DEX PS DDS Applicator System (700 μg dexamethasone) compared with the 350 μg DEX PS DDS Applicator System (350 μg dexamethasone) in the treatment of non-infectious ocular inflammation of the posterior segment in patients with Anterior uveitis. (700 μg dexamethasone vs. 350 μg dexamethasone)

Study results are currently being analyzed. Please visit this webpage next month for the study update.

For more information:

http://www.clinicaltrials.gov

 

Contact Us

Dr. C. Michael Samson, Principal Investigator

Katy Tai, Research ManagerTel: (212) 979-4251

Address310 E. 14th StreetNew York, NY 10003

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