Plaque Psoriasis
Conditions
Brief summary
The primary objective of this study is to evaluate the efficacy of multiple-dose HSK47388 versus placebo in participants with moderate-to-severe plaque psoriasis.
Interventions
DRUGHSK47388
HSK47388 tablets will be administered orally, once a day
Sponsors
Haisco Pharmaceutical Group Co., Ltd.
Study design
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
QUADRUPLE (Subject, Caregiver, Investigator, Outcomes Assessor)
Eligibility
Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No
Inclusion criteria
1. Confirmed diagnosis of plaque psoriasis with a disease duration of at least 26 weeks before the first administration of the study intervention 2. Total Body Surface Area (BSA) involvement ≥ 10% at both screening and baseline visits 3. Psoriasis Area and Severity Index (PASI) total score ≥ 12 at both screening and baseline visits 4. Investigator Global Assessment (IGA) for plaque psoriasis total score ≥ 3 (moderate or severe disease) at both screening and baseline visits 5. Participants deemed appropriate candidates for systemic therapy for plaque psoriasis
Exclusion criteria
1. Non-plaque psoriasis (e.g., erythrodermic, guttate, or pustular psoriasis) 2. Current drug-induced psoriasis 3. Current diagnosis, signs, or symptoms of severe, progressive, or uncontrolled disease involving the renal, hepatic, cardiac, vascular, pulmonary, gastrointestinal, endocrine, neurologic, hematologic, rheumatologic, psychiatric, or metabolic systems 4. Known allergy, hypersensitivity, or intolerance to HSK47388。 5. A history of malignant tumor before screening; 6. Subjects deemed unsuitable for participation due to other factors as determined by the investigator
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| HSK47388 and Placebo Group: Percentage of Participants Achieving PASI 75 Response From Baseline to week 16 | 16 weeks | Percentage of participants achieving PASI 75 response (\>=75% improvement in PASI from baseline) at Week 16 will be reported. The PASI is a system for assessing/grading psoriatic lesion severity and treatment response. It divides the body into 4 regions (head, trunk, upper extremities, lower extremities), with each region separately scored for erythema, induration, scaling (0-4 scale each) and involvement extent (0-6 scale). PASI yields a 0-72 numeric score, where higher scores mean more severe disease. |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| HSK47388 and placebo Group: Percentage of Participants Achieving an IGA Score of 0 or 1 and >=2 Grade Improvement From Baseline at Weeks 16 | 16 weeks | The percentage of participants with IGA 0/1 and ≥2-grade improvement from baseline at Weeks 16 will be reported. IGA is investigators' assessment of participants' psoriasis at a specific time point, grading overall lesions by induration, erythema, scaling, and categorizing psoriasis as cleared (0), minimal (1), mild (2), moderate (3), or severe (4). |
| Change From Baseline in Body Surface Area (BSA) at Week 16 | 16 weeks | Change from baseline in BSA at Week 16 will be reported. BSA is a common measure of skin disease extent, defined as the percentage of total body surface area affected by the target condition (i.e., plaque psoriasis). |
| HSK47388 and Placebo Group: Change From Baseline in Total DLQI Score at Week 16 | 16 weeks | Change from baseline in total DLQI score at Week 16 will be reported. The DLQI is a dermatology-specific HRQoL instrument designed to assess a disease's impact on participants' HRQoL. It is a 10-item questionnaire evaluating HRQoL over the past week; in addition to overall HRQoL, it assesses 6 quality-of-life domains: symptoms/feelings, daily activities, leisure, work/school performance, personal relationships, and treatment. Total scores range from 0 to 30, with higher scores indicating greater HRQoL impact. |
| Number of Participants with Adverse Events (AEs) | 20 weeks | An adverse event (AE) is any untoward medical event that occurs in a participant administered an investigational product, and it does not necessarily indicate only events with clear causal relationship with the relevant investigational product. |
Outcome results
None listed