TrialPath
← Back to searchRecruiting

A Study of WD-890 in Participants With Moderate-to-Severe Plaque Psoriasis

NCT06912165 · Zhejiang Wenda Pharma Technology LTD.
In plain English

Click the button to translate this study into plain language — what it is, who qualifies, and what participation looks like.

Official title
A Multicenter, Randomized, Double-Blind, Placebo-Controlled Phase II Study to Evaluate the Efficacy and Safety of WD-890 Tablets for the Treatment of Moderate to Severe Plaque Psoriasis
About this study
The total duration of this study is up to 24 weeks which includes a screening period of less than or equal to (\<=) 4 weeks, a 16-week treatment period, and a 4-week safety follow-up period. Aged 18 to 70 years (inclusive) were enrolled in this study. Participants were randomized to receive WD-890 or placebo.
Eligibility criteria
Inclusion Criteria: * Male or female participant aged 18 to 70 years(inclusive)at the time of informed consent. * Diagnosis of plaque psoriasis for at least 6 months prior to the screening visit. ≥10% of BSA involvement at screening visit and randomization; * Psoriasis Area and Severity Index (PASI) score ≥12 and static Physician's Global Assessment (sPGA) ≥3 at screening visit and randomization Exclusion Criteria: * Participant has a nonplaque form of psoriasis (for example, erythrodermic, guttate, inverse, pustular,or drug induced psoriasis.) * Has uncontrolled arterial hypertension characterized by a systolic blood pressure (BP) ≥160 mm Hg or diastolic BP ≥100 mm Hg Note: Determined by 2 consecutive elevated readings. If an initial BP reading exceeds this limit, the BP may be repeated once after the subject has rested sitting for ≥10 minutes. If the repeat value is less than the criterion limits, the second value may be accepted * Class III or IV congestive heart failure by New York Heart Association Criteria * Participant with a history of chronic bacterial infections (e.g., chronic pyelonephritis, chronic bronchiectasis, or chronic osteomyelitis).
Study design
Enrollment target: 140 participants
Allocation: randomized
Masking: double
Age groups: adult, older_adult
Timeline
Starts: 2024-12-31
Estimated completion: 2025-11-30
Last updated: 2025-04-11
Interventions
Drug: WD-890 tabletDrug: WD-890 tabletDrug: WD-890 tabletDrug: Placebo
Primary outcomes
  • Percentage of Participants Achieving Psoriasis Area Severity Index (PASI) 75 Score at Week 16 (Screening up to Week 16)
Sponsor
Zhejiang Wenda Pharma Technology LTD. · other
Contacts & investigators
ContactQianjin Lu, doctor · contact · qianlu5860@pumcderm.cams.cn · +86 137 8709 7676
All locations (1)
Hospital for Skin Diseases, Institute of Dermatology, Chinese Academy of Medical Sciences, Peking Union Medical CollegeRecruiting
Nanjing, Jiangsu, China
A Study of WD-890 in Participants With Moderate-to-Severe Plaque Psoriasis · TrialPath