drugset / Trial / NCT05772520

The Efficacy and Safety of TLL018 in Moderate-to-severe Plaque Psoriasis

NCT05772520

Phase 2 Completed 82 enrolled Hangzhou Highlightll Pharmaceutical Co., Ltd
RandomizedParallel-groupTriple-blindTreatment

Summary

This is a Phase 2, multicenter, randomized, double-blinded, parallel dose group, placebo-controlled, dose-ranging study to evaluate the efficacy and safety of 2 doses of TLL018 as therapy in approximately 90 participants with moderate-to-severe PP.

Timeline

Start
2023-01-19
Primary completion
2024-12-01
Completion
2024-12-23

Drugs

EvaluationDrugModalityDoseRoute
Subject TLL018 Unknown 20 mg Oral
Subject TLL018 Unknown 40 mg Oral

Indications