TTrialPathMatch Me to Trials
← Back to trials
RecruitingPsoriasis

Evaluate the Safety and Pharmacokinetics/Pharmacodynamics of HS-20118

Eligible age

18–65 yrs

Accepts

All genders

Locations

2 states

Healthy volunteers

Yes

See if you qualify for this study

Answer a few quick questions about your location and health. Takes about a minute.

Check my eligibility →

About this study

The study will be conducted in 2 parts (SAD 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 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 .

Sponsor: Jiangsu Hansoh Pharmaceutical Co., Ltd.

You may qualify if…

  • For the SAD study:
  • 1. Healthy adults aged 18-45 years (inclusive) at the time of signing the informed consent form;
  • 2. Male participants weighing ≥ 50 kg and female participants weighing ≥ 45 kg, both ≤ 110 kg; body mass index (weight/square of height (kg/m2)) within the range of 18-28 kg/m2 (inclusive);
  • 3. Normal results or abnormal results but without clinical significance in comprehensive examinations, including general physical examination, vital signs, laboratory tests, 12-lead ECG, abdominal color Doppler ultrasound, and chest X-ray from the frontal and lateral position ;
  • For the MAD study:
  • 1. Male or female participants aged 18-65 years (inclusive) at the time of signing the informed consent form;
  • 2. Male participants weighing ≥ 50 kg and female participants weighing ≥ 45 kg, both ≤ 110 kg;
  • 3. Chronic plaque psoriasis for at least 6 months with or without psoriatic arthritis;

You may not qualify if…

  • For the SAD study:
  • 1. Participants with immune-related diseases and medical history at screening;
  • 2. Participants with a history of drug or other allergies who are considered by the investigator to be at high risk for participating in this study, or who may be allergic to the investigational medicinal product or any component of the investigational medicinal product as judged by the investigator;
  • 3. History of drug abuse within the past 5 years or use of illicit drugs within 3 months before the study; or positive for urine drug screening;
  • For the MAD study:
  • 1. Guttate psoriasis, pustular psoriasis, erythrodermic psoriasis, drug-induced psoriasis, or other diseases that affect the treatment results;
  • 2. Current use of illicit drugs or prior use of illicit drugs within the specific time periods;
  • 3. Known history of recurrent or chronic infections, or prior history of chronic or recurrent infections, including but not limited to: chronic renal infection, chronic chest infection (e.g., bronchiectasis), symptomatic urinary tract infection, and open, draining, or infected skin wounds; history of serious infections (e.g., sepsis, pneumonia, and pyelonephritis), or hospitalization or treatment with intravenous antibiotics for infections within 2 months before screening;

Where it's recruiting

California

Anaheim

Florida

Miami Lakes · Pompano Beach

Source: ClinicalTrials.gov · NCT06846710 · last updated 2025-08-07

Evaluate the Safety and Pharmacokinetics/Pharmacodynamics of HS-20118 · TrialPath