BENITIONSClinical Trial Intelligence

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

Phase 2 Completed NCT05772520

ConditionPlaque Psoriasis
PhasePhase 2
SponsorHangzhou Highlightll Pharmaceutical Co., Ltd
StatusCompleted
Enrollment82 participants
InterventionsTLL018 tablets
Start dateJan 19, 2023
Completion dateDec 1, 2024
Results postedJul 21, 2026

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.

Proportion of Participants Achieving PASI-75 (FAS)

Week12 · Participants

Cohort 111 Participants
Cohort 213 Participants
Cohort 34 Participants
Cohort 43 Participants

Proportion of Participants Achieving PASI 75 (PPS)

Week12 · Participants

Cohort 19 Participants
Cohort 211 Participants
Cohort 34 Participants
Cohort 42 Participants

Open in BENITIONS View on ClinicalTrials.gov

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