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Clinical Trials in China / NCT06912165
Recruiting Phase 2

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

NCT06912165 · tracked via the Priya Life Science China tracker
Sponsor
Zhejiang Wenda Pharma Technology LTD.
Phase
Phase 2
Started
2024-12-31
Last updated
2025-04-11

Condition(s) studied

Brief Description of Focus of Study

Investigational drug(s) / intervention(s)

WD-890 tabletWD-890 tabletWD-890 tabletPlacebo

WD-890 tablet: Participants will receive WD-890 Dose 1 QD and placebo from Week 0 through Week 16. Participants will receive placebo to maintain the blinding of dose regimens.

WD-890 tablet: Participants will receive WD-890 Dose 2 QD and placebo from Week 0 through Week 16. Participants will receive placebo to maintain the blinding of dose regimens.

WD-890 tablet: Participants will receive WD-890 Dose 3 QD and placebo from Week 0 through Week 16. Participants will receive placebo to maintain the blinding of dose regimens.

Placebo: Participants will receive placebo QD from Week 0 through Week 16.

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

Sex
ALL
Min age
18 Years
Max age
70 Years
Healthy volunteers
No
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).

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
Hospital for Skin Diseases, Institute of Dermatology, Chinese Academy of Medical Sciences, Peking Union Medical College Nanjing Jiangsu Recruiting

More Zhejiang Wenda Pharma Technology LTD. trials in China

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT06912165 on ClinicalTrials.gov ↗ ← All trials in China