Lilly to appeal FDA's approvable letter for Arxxant

Share this article:
Eli Lilly says it will appeal the FDA's decision to issue an "approvable letter" that requests an additional efficacy study for Arxxant, its new drug for moderate to severe nonproliferative diabetic retinopathy. Its appeal will be based on unmet medical need for the drug, demonstrated efficacy and Arxxant's "robust safety profile."

This material may not be published, broadcast, rewritten or redistributed in any form without prior authorization. Your use of this website constitutes acceptance of Haymarket Media's Privacy Policy and Terms & Conditions