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Study identifier: NCT07033234 Synced from ClinicalTrials.gov · July 30, 2026
● Recruiting

Evaluate the Safety and Pharmacokinetics/Pharmacodynamics and Food Effect of HS-20118

Condition: Psoriasis  ·  Sponsor: Jiangsu Hansoh Pharmaceutical Co., Ltd.

PhasePhase 1
Planned participants142
Who can joinAll sexes, 18 Years to 65 Years
Healthy volunteersYes

About this study

The study will be conducted in 2 parts (SAD and FE for Part 1 and MAD for Part2). Part 1 is a single-center, randomized, double-blind, placebo-controlled, SAD study to evaluate the safety, tolerability, immunogenicity, and PK of HS-20118 and explore the food effect and fasting time on PK after a single oral dose in healthy participants. Part 2 is a multi-center, randomized, double-blind, placebo-controlled, MAD study to evaluate the safety, tolerability, immunogenicity, PK, and PD of HS-20118 after multiple oral doses in patients with moderate to severe plaque psoriasis.

This description comes directly from the study's public registry record.

Talk to the study team

Liming Wu Director of Dermatology  ·  +86 13750837205  ·  18957118053@163.com

Ying Wang Director of GCP Office  ·  +86 18367124548  ·  nancywangying@163.com

Always discuss trial participation with your own doctor first.

Locations (1)

Affiliated Hangzhou First People's HospitalHangzhou, Zhejiang, ChinaRecruiting

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Source record: clinicaltrials.gov/study/NCT07033234