Aclaris Therapeutics reports positive Phase 1b data for ATI‑052 in atopic dermatitis and asthma

Aclaris Therapeutics announced that its investigational antibody ATI‑052 produced statistically significant improvements in a Phase 1b trial for severe atopic dermatitis and a separate Phase 1b trial for mild‑to‑moderate asthma. The atopic dermatitis study showed a 45% placebo‑adjusted gain in EASI score and 43% itch relief, while the asthma study reported a 59% reduction in FeNO and a 200 ml increase in FEV1. The company said the safety profile was favorable and said it will prioritize a Phase 2b trial in eosinophilic esophagitis in early 2027.

The positive proof‑of‑concept data could advance ATI‑052 toward later‑stage trials and broaden Aclaris’ pipeline, while the stock fell 9.5% in pre‑market trading after the announcement, reflecting market reaction to the early‑stage results.

  • 1The atopic dermatitis trial enrolled 14 patients, with a 3:1 randomization to ATI‑052 versus placebo.
  • 2Patients received five weekly doses of 480 mg ATI‑052 over four weeks.
  • 3ATI‑052 achieved a 45% placebo‑adjusted improvement in the EASI score at Day 57.
  • 4Itch relief was 43% placebo‑adjusted at Day 57.
  • 5The asthma trial enrolled 16 patients with elevated baseline FeNO.
  • 6A single 480 mg dose produced a 59% mean reduction in FeNO by Day 15 versus 15% for placebo.

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