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

Last updated: April 8, 2025
Sponsor: Zhejiang Wenda Medical Technology Co., Ltd.
Overall Status: Active - Recruiting

Phase

2

Condition

Rosacea

Warts

Rash

Treatment

WD-890 tablet

Placebo

Clinical Study ID

NCT06912165
WENDA890PSO-001
  • Ages 18-70
  • All Genders

Study Summary

Th purpose of the study is to evaluate the dose response of WD-890 in efficacy at Week 16 in participants with moderate-to-severe plaque psoriasis.

Eligibility Criteria

Inclusion

Inclusion Criteria:

  • Male or female participant aged 18 to 70 years(inclusive)at the time of informedconsent.

  • 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 GlobalAssessment (sPGA) ≥3 at screening visit and randomization

Exclusion

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 consecutiveelevated readings. If an initial BP reading exceeds this limit, the BP may berepeated once after the subject has rested sitting for ≥10 minutes. If the repeatvalue 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., chronicpyelonephritis, chronic bronchiectasis, or chronic osteomyelitis).

Study Design

Total Participants: 140
Treatment Group(s): 2
Primary Treatment: WD-890 tablet
Phase: 2
Study Start date:
December 31, 2024
Estimated Completion Date:
November 30, 2025

Study Description

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.

Connect with a study center

  • Hospital for Skin Diseases, Institute of Dermatology, Chinese Academy of Medical Sciences, Peking Union Medical College

    Nanjing, Jiangsu 210000
    China

    Active - Recruiting

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