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Evaluate the Safety and Pharmacokinetics/Pharmacodynamics of HS-20118

NCT06846710 · Jiangsu Hansoh Pharmaceutical Co., Ltd.
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Official title
A Phase I Clinical Study to Evaluate the Safety, Tolerability, Immunogenicity, Pharmacokinetics, and Pharmacodynamics of Single and Multiple Ascending Doses of HS-20118 in Adult Participants
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 1 will consist of 5 cohorts, i.e., X1 mg, X2 mg, X3 mg, X4 mg, and X5 mg dose cohorts (each cohort will include 3 participants to receive placebo). There will be no restriction on the male-to-female ratio. Each cohort will include 12 participants (HS-20118:placebo = 9:3), with a total of 60 participants. Participants will undergo PK blood sampling, ADA blood sampling, PD blood sampling and safety examinations during the study. 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. Part 2 will tentatively consist of 6 cohorts ( HS-20118 vs placebo = 9:3), i.e., (1) A1 mg, (2) A2 mg, (3) A3 mg, (4) A4 mg, (5) A5 mg, (6) A6 mg. Each cohort will include 12 participants (HS-20118:placebo = 9:3), with a total of 72 participants. There will be no restriction on the male-to-female ratio. Participants will undergo PK blood sampling, ADA blood sampling, PD blood sampling and safety examinations during the study.
Eligibility criteria
Inclusion Criteria: 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; Exclusion Criteria: 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;
Study design
Enrollment target: 132 participants
Allocation: randomized
Masking: double
Age groups: adult, older_adult
Timeline
Starts: 2025-05-02
Estimated completion: 2027-02-28
Last updated: 2025-08-07
Interventions
Drug: HS-20118Other: HS-20118 placebo
Primary outcomes
  • Incidence, severity and association with the study drug of adverse events (AEs), serious AEs (SAEs), and AEs leading to discontinuation (Day 1 up to Day 36 (SAD), Day 1 up to Day 71 (MAD))
  • Number of participants with abnormalities of physical examination (Day 1 up to Day 36 (SAD), Day 1 up to Day 71 (MAD))
  • Number of participants with abnormalities of vital signs (Day 1 up to Day 36 (SAD), Day 1 up to Day 71 (MAD))
Sponsor
Jiangsu Hansoh Pharmaceutical Co., Ltd. · industry
All locations (9)
Kinetic Clinical ResearchNot Yet Recruiting
Anaheim, California, United States
Clinitiative - Floridian Clinical Research, LLCNot Yet Recruiting
Miami Lakes, Florida, United States
NuLine Clinical Trial Center (Network)Not Yet Recruiting
Pompano Beach, Florida, United States
Pacific Clinical Research Network (PCRN), AucklandRecruiting
Takapuna, Auckland, New Zealand
Pacific Clinical Research Network (PCRN), ChristchurchNot Yet Recruiting
Christchurch, Christchurch, New Zealand
Momentum Clinical Research, DunedinNot Yet Recruiting
Dunedin, Dunedin, New Zealand
Momentum Clinical Research, PukekoheNot Yet Recruiting
Pukekohe, Pukekohe, New Zealand
Pacific Clinical Research Network (PCRN), WellingtonNot Yet Recruiting
Upper Hutt, Upper Hutt, New Zealand
Momentum Clinical Research, WellingtonNot Yet Recruiting
Mount Cook, Wellington Region, New Zealand
Evaluate the Safety and Pharmacokinetics/Pharmacodynamics of HS-20118 · TrialPath