This study is a Phase 2a/b, randomized, double-blind, placebo-controlled, multicenter trial designed to evaluate the efficacy, safety, tolerability and dose-response relationship of DDY391 in participants with active moderate to severe PsA.
The study is composed of two sequential parts:
* Part A to evaluate efficacy, safety and tolerability of DDY391 compared with placebo.
* Part B to determine the dose-response relationship of multiple doses of DDY391 compared with placebo.