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Study details
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Evaluate the Safety and Pharmacokinetics/Pharmacodynamics of HS-20118

Jiangsu Hansoh Pharmaceutical Co., Ltd.
NCT IDNCT06846710ClinicalTrials.gov data as of Apr 2026
Phase

Phase 1

Target enrollment

132

Study length

about 1.8 years

Ages

18–65

Locations

3 sites in CA, FL

What this study is about

Researchers are testing a treatment for psoriasis. The trial will evaluate how safe, tolerable, and effective this treatment is in healthy adults and people with moderate to severe plaque psoriasis.

Simplified from trial records by PatientMatch.

What you may be asked to do

  • 1.HS-20118 placebo
  • 2.Take HS-20118

Participation Burden

What's physically and logistically required of participants.

Logistics & Travel
In-person visits

Requires travel to a study site

Physical Intervention
Standard

How treatment is administered

Treatment Assignment
Randomized & Blinded

You may get a placebo/standard care, and you won't know which.

Extracted study details

Pulled from the trial record to show what is being tested and what the study is measuring.

Endpoints

Primary: Incidence, severity and association with the study drug of adverse events (AEs), serious AEs (SAEs), and AEs leading to discontinuation, Number of participants with clinical laboratory abnormalities

Secondary: AUC, Change from baseline in body surface area (BSA), Change from baseline in dermatology life quality index (DLQI), Change from baseline in psoriasis area and severity index (PASI) total score, Cmax, Tmax

Body systems

Dermatology