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Third PharmacoSurgery(TM) Platform Product Candidate in Clinical Trials
SEATTLE, Sept. 9 /PRNewswire/ -- Omeros Corporation today announced that it is enrolling patients in a Phase 1/Phase 2 study of OMS302, the Company's third PharmacoSurgery(TM) product candidate, for use during ophthalmologic surgery. At least 60 patients undergoing age-related cataract extraction with lens replacement are planned for enrollment in the study.
"With the initiation of this study, all three of Omeros' current PharmacoSurgery product candidates are now in the clinic," said Gregory A. Demopulos, M.D., Chairman and CEO of Omeros. "Each of the two agents in OMS302 is currently used individually and perioperatively during eye surgery. OMS302 combines these two agents and their pharmacologic activities into a single proprietary product candidate. With approximately three million cataract procedures performed annually in the U.S. alone, OMS302 is designed to address a large and growing market."
The Phase 1/Phase 2 trial is a randomized, double-blind, vehicle-controlled and parallel-assigned study evaluating the effects of OMS302 on dilation of the pupil during cataract surgery and on pain, discomfort and inflammation following the procedure. OMS302 is added to standard irrigation solutions used in ophthalmologic surgery and is delivered directly to the eye during the operation.
PharmacoSurgery(TM) product candidates are proprietary combinations of
therapeutic agents designed to act simultaneously at multiple discrete
targets to preemptively block the molecular-signaling and biochemical
cascade caused by surgical trauma and to provide clinical benefits both
during and after surgery. The lead product candidate in the
PharmacoSurgery(TM) platform is OMS103HP, which is currently in two Phase 3
clinical programs evaluating its safety and ability to improve
postoperative joint function and reduce pain following arthroscopic
surgery. The urological PharmacoSurgery
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