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

RecruitingPhase 2Ages 18 Years - 70 YearsAllZhejiang Wenda Pharma Technology LTD.
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In plain words

What the trial is, and whether it could suit you

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.

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๐Ÿ“‹ Eligibility rules (as published)
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. โ‰ฅ10% of BSA involvement at screening visit and randomization; * Psoriasis Area and Severity Index (PASI) score โ‰ฅ12 and static Physician's Global Assessment (sPGA) โ‰ฅ3 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) โ‰ฅ160 mm Hg or diastolic BP โ‰ฅ100 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 โ‰ฅ10 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).
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What it tests

  • WD-890 tablet
  • WD-890 tablet
  • WD-890 tablet
  • Placebo
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Where

1 site
Hospital for Skin Diseases, Institute of Dermatology, Chinese Academy of Medical Sciences, Peking Union Medical College
Nanjing, China
๐Ÿค Taking part is your choice, and you can leave at any time. Only the trial team can confirm you are eligible โ€” always decide together with your own doctor.
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