Aqilion has completed Phase 1 study with AQ280 within the Regulus program
AQILION (publ) announces today that it has successfully completed the first clinical study in humans within the Regulus program. The Phase 1 ARIA-1 study was conducted to evaluate the safety, tolerability, and pharmacokinetics of the drug candidate AQ280 in healthy adult participants, given in single dose and repeated dosing. The preliminary study results are expected in Q4 2023.Within the Regulus program, Aqilion is developing AQ280, which is a super selective JAK1 inhibitor, as a treatment of the chronic disease eosinophilic esophagitis. Since August last year, healthy volunteers have