
Jennifer Barrett writes, "The FDA’s approval is based on data from the global LIBERTY AD clinical
program, which included 3, phase 3 trials that examined the use of
Dupixent either alone or with topical corticosteroids in patients with
inadequately controlled moderate-to-severe AD. Dupixent alone or with
topical corticosteroids met its primary and key secondary endpoints in
all trials."
Learn more about this new drug by reading the full article HERE!
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