EyePoint Pharmaceuticals Inc. CEO Nancy Lurker noted that the US FDA’s early approval of the firm’s posterior uveitis therapy Yutiq, weeks ahead of a Nov. 5 action date, gives EyePoint the opportunity to promote and highlight the product during the American Association of Ophthalmology (AAO) meeting at the end of October.
“AAO is the largest gathering of ophthalmologists in the world, and we planned meticulously for this meeting in anticipation of a possible early approval,” the exec said during an Oct. 15 call on the approval. Yutiq is a non-bioerodible, single-dose intravitreal micro-insert of 0
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