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Investors sceptical of Iluvien 36 month data in DMO

This article was originally published in Scrip

Executive Summary

While the much-anticipated 36-month data from Alimera Sciences' 956-patient Phase III FAME studies of Iluvien (fluocinolone acetonide intravitreal insert), which the company licensed from partner pSivida, demonstrated improvement in best corrected visual acuity (BCVA) of 15 letters from baseline in patients with diabetic macular oedema (DMO), the A and B trials failed individually to reach statistical significance.

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This copy is for your personal, non-commercial use. For high-quality copies or electronic reprints for distribution to colleagues or customers, please call +44 (0) 20 3377 3183

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