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ISTA Pharmaceuticals Reports Third Quarter 2010 Financial Results

e is ready to launch BROMDAY this month.  We expect to discontinue the twice-daily XIBROM (bromfenac ophthalmic solution)® 0.09% product in early 2011."

Continued Anido, "With our newest product pipeline developments, we have proven our ability to extract significant additional value from our core therapeutic compounds, bromfenac and bepotastine.  In addition to gaining approvals for BROMDAY and BEPREVE™, we initiated our REMURA™ (bromfenac ophthalmic solution for dry eye) Phase 3 clinical program, plus released the positive results of our Phase 1/2 bepotastine besilate nasal spray study.  Based upon these Phase 1/2 results, we plan to submit an Investigational New Drug (IND) Application to the FDA for bepotastine nasal spray to initiate Phase 2 clinical studies before the end of 2010.  In addition, we expect to report the results of the REMURA Phase 3 dry eye efficacy study in the middle of 2011.  Gaining approval for both product candidates would allow us to participate in significantly larger market segments than those for ISTA's current product offerings.  To complement our eye care and allergy franchises, we continue to evaluate acquiring both late-stage drug candidates to add to our pipeline and marketed products to add to our sales portfolio, assets that have the potential to deliver significant value to our stakeholders for years to come."Net Revenues

(In millions, except percentage data)Three Months Ended

September 30,

Nine Months Ended

September 30,2010





























120%Product sales, net





SOURCE ISTA Pharmaceuticals, Inc.
Copyright©2010 PR Newswire.
All rights reserved

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