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临床试验/CTIS2023-508992-35-00
CTIS2023-508992-35-00进行中(未招募)1 期

A Phase 2b Multicenter, Randomized, Double-blind, Placebo-controlled Dose-Ranging Study to Evaluate the Efficacy and Safety of JNJ-81241459 for the Treatment of Participants with Moderate to Severe Plaque Psoriasis

Janssen Cilag International0 个研究点目标入组 200 人开始时间: 2024年1月16日最近更新:
适应症

试验速览

阶段
1 期
状态
进行中(未招募)
入组人数
200

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional

入排标准

年龄范围
18 至 65+(—)
性别
All

入选标准

  • Be =18 (or the legal age of consent if it is higher in the jurisdiction in which the study is taking place) years of age at screening, inclusive., Diagnosis of plaque psoriasis, Total BSA =10% at screening and baseline., Total PASI =12 at screening and baseline., Total IGA =3 at screening and baseline.

排除标准

  • Nonplaque form of psoriasis (eg, erythrodermic, guttate, or pustular)., Current drug-induced psoriasis (eg, a new onset of psoriasis or an exacerbation of psoriasis from beta blockers, calcium channel blockers, or lithium)., A current diagnosis or signs or symptoms of severe, progressive, or uncontrolled renal, liver, cardiac, vascular, pulmonary, gastrointestinal, endocrine, neurologic, hematologic, rheumatologic, psychiatric, or metabolic disturbances., A current diagnosis or history of IBD., Known allergies, hypersensitivity, or intolerance to JNJ-81241459 or its excipients (refer to the JNJ-81241459 IB).

研究者

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