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临床试验/NCT05174065
NCT05174065已完成3 期

A Phase 3, Multicenter, Randomized, Double-blind, Placebo-controlled Study to Evaluate the Efficacy and Safety of Apremilast (AMG 407) in Japanese Subjects With Palmoplantar Pustulosis (PPP)

Amgen40 个研究点 分布在 1 个国家目标入组 176 人开始时间: 2022年3月8日最近更新:
适应症
干预措施
相关药物

试验速览

阶段
3 期
状态
已完成
发起方
Amgen
入组人数
176
试验地点
40
主要终点
Percentage of Participants Who Achieved at Least a 50% Reduction From Baseline in Palmoplantar Pustulosis Area and Severity Index (PPPASI) Total Score (PPPASI-50) at Week 16

研究概览

简要总结

The primary objective of the study is to evaluate the efficacy of apremilast (AMG 407) twice daily (BID) compared with placebo in participants with Palmoplantar Pustulosis (PPP).

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
Double (Participant, Investigator)

入排标准

年龄范围
18 Years 至 99 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • 未提供

排除标准

  • 未提供

研究组 & 干预措施

Apremilast

Experimental

Apremilast will be administered to participants twice daily (BID)

干预措施: Apremilast (Drug)

Placebo and Apremilast

Experimental

Matching placebo will be administered to participants twice daily (BID) until week 16. After week 16, Apremilast will be administered to participants BID.

干预措施: Apremilast (Drug)

Placebo and Apremilast

Experimental

Matching placebo will be administered to participants twice daily (BID) until week 16. After week 16, Apremilast will be administered to participants BID.

干预措施: Placebo (Drug)

结局指标

主要结局

Percentage of Participants Who Achieved at Least a 50% Reduction From Baseline in Palmoplantar Pustulosis Area and Severity Index (PPPASI) Total Score (PPPASI-50) at Week 16

时间窗: Baseline and Week 16

A PPPASI 50 response is defined as a ≥ 50% reduction in PPPASI total score from baseline. The PPPASI is a system used for assessing and grading the severity (in terms of erythema, pustules/vesicle and desquamation/scale) and area of PPP lesions and their response to therapy. The PPPASI produces a numeric score that can range from 0 to 72, with a higher score indicating more severe disease. Participants who discontinued investigational product before week 16 due to lack of efficacy, adverse event, or use of protocol-prohibited medication (intercurrent events) were to be considered as treatment failures as the result of the intercurrent event and the PPPASI-50 values for visits on and after the intercurrent event were imputed as non-responders. The missing PPPASI-50 values due to the other reasons were imputed using the multiple imputation method.

次要结局

  • Change From Baseline in PPPASI Total Score at Week 16(Baseline and Week 16)
  • Change From Baseline in Palmoplantar Pustulosis Severity Index (PPSI) Total Score at Week 16(Baseline and Week 16)
  • Change From Baseline in VAS Assessment for PPP Symptoms (Pain/Discomfort) at Week 16(Baseline and Week 16)
  • Change From Baseline in Visual Analogue Scale (VAS) Assessment for PPP Symptoms (Pruritus) at Week 16(Baseline and Week 16)
  • Number of Participants Who Experienced a Treatment-emergent Adverse Event (TEAE)(Placebo-controlled period: Day 1 to Week 16; Apremilast exposure period : Apremilast Day 1 to a maximum of Week 52 (plus 4 weeks safety follow-up))
  • Change From Baseline in Dermatology Life Quality Index (DLQI) Total Score at Week 16(Baseline and Week 16)

研究者

发起方
Amgen
申办方类型
Industry
责任方
Sponsor

研究点 (40)

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