This is a randomized, double-blind study comparing LNK01001 to placebo in participants with moderately to severely atopic dermatitis who were candidates for systemic therapy (ie, patients with a history of inadequate response to topical treatments, those who were using a systemic treatment, or those for whom topical treatments are otherwise medically inadvisable). The objective of this study is to evaluate the efficacy and safety of LNK01001 in adult patients with moderate to severe AD who are candidates for systemic therapy.
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Eczema Area and Severity Index (EASI-75) at Week 16
Timeframe: Baseline and Week 16
Investigator's Global Assessment (IGA) score of 0/1 at Week 16
Timeframe: Baseline and Week 16