Lumithera CEO Discusses FDA Authorization for Veleda for Dry AMD

from Eyewire News: The Podcast · host Eyewire News

The CEO of Lumithera joins us to discuss the FDA authorization of the Veleda system for dry AMD; the FDA accepts the resubmitted NDA for dry eye disease candidate reproxalap; and Alcon launches the first contact lens designed for a 1-week replacement cycle. Learn more about your ad choices. Visit megaphone.fm/adchoices

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This episode was published on November 20, 2024.

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