Dermira receives fast track designation from FDA for lebrikizumab for the treatment of atopic dermatitis

Dermira

10 December 2019 - Dermira today announced that the U.S. FDA has granted fast track designation for lebrikizumab, its novel, investigational treatment being evaluated for patients with moderate-to-severe atopic dermatitis.

Lebrikizumab is currently being evaluated in two Phase 3 studies, ADvocate 1 and ADvocate 2, to confirm its safety and efficacy in adolescent and adult patients, ages 12 years and older, with moderate-to-severe atopic dermatitis.

Read Dermira press release

Michael Wonder

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Michael Wonder

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Medicine , US , Fast track