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临床试验/NCT01406938
NCT01406938已完成3 期

A Randomized, Double-blind, Multicenter Study of Subcutaneous Secukinumab, Assessing Psoriasis Area and Severity Index (PASI) Response and Maintenance of Response in Subjects With Moderate to Severe Chronic Plaque-type Psoriasis on Either a Fixed Dose Regimen or on a Retreatment at Start of Relapse Regimen

Novartis Pharmaceuticals1 个研究点 分布在 1 个国家目标入组 967 人开始时间: 2011年8月最近更新:
适应症
干预措施
相关药物

试验速览

阶段
3 期
状态
已完成
入组人数
967
试验地点
1
主要终点
For the Fixed Interval Group and the Start of Relapse (SoR) Group, the Percentage of Participants (Who Responded to Treatment at Week 12) Maintaining a 75% Improvement From Baseline in Psoriasis Area and Severity Index (PASI) Score at Week 52

研究概览

简要总结

This study will assess the safety and efficacy of two different doses and two different dose regimens of subcutaneous secukinumab in patients that have moderate to severe, chronic, plaque-type psoriasis.

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
Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)

入排标准

年龄范围
18 Years 至 —(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

AIN457150 mg- Induction period Only(IPO)

Experimental

secukinumab 150 mg (1 injection per dose) and placebo to secukinumab 150 mg (1 injection per dose). Induction period only (IPO)

干预措施: AIN457 150mg (Drug)

AIN457 300 mg - IPO

Experimental

secukinumab- 2 x 150mg injections per dose

干预措施: AIN457 300mg (Drug)

AIN457 150 mg - Fixed Interval (FI)

Experimental

1 s.c. secukinumab 150 mg injection + 1 s.c. PBO (placebo) secukinumab injection

干预措施: AIN457 150mg (Drug)

AIN457 300 mg FI

Experimental

2 s.c. secukinumab 150 mg injections

干预措施: AIN457 300mg (Drug)

AIN457 150 mg- Start of relapse (SoR)

Experimental

1 s.c. secukinumab 150 mg injection + 1 s.c. PBO secukinumab injection

干预措施: AIN457 150mg (Drug)

AIN457 300 mg- SoR

Experimental

2 s.c. secukinumab 150 mg injections

干预措施: AIN457 300mg (Drug)

结局指标

主要结局

For the Fixed Interval Group and the Start of Relapse (SoR) Group, the Percentage of Participants (Who Responded to Treatment at Week 12) Maintaining a 75% Improvement From Baseline in Psoriasis Area and Severity Index (PASI) Score at Week 52

时间窗: Week 40 , week 52

PASI: Combined assessment of lesion severity and affected area into a single score: 0 (no disease) to 72(maximal disease). Body is divided into 4 areas for scoring (head, arms, trunk, legs; each area is scored by itself and scores are combined for final PASI. For each area, percent of skin involved is estimated: 0 (0%) to 6 (90-100%), and severity is estimated by clinical signs, erythema, induration and desquamation; scale 0 (none) to 4 (maximum). Final PASI = sum of severity parameters for each area\* area score weight of section(head: 0.1, arms: 0.2 body: 0.3 legs: 0.4)

次要结局

  • Percent of Participants Achieving Psoriasis Area & Severity Index (PASI) Score and IGA Mod 2011 0 or 1 Score Over Time at Week 12 and 52 (Maintenance Period))(Baseline, week 16,20,24,28,32,36,40,44,48, and Week 52)
  • % of Participants Achieving a DLQI Score of 0 or 1 at Each Visit up to Week 52, (Maintenance).(Baseline to week 16, 20, 24, 28, 32, 36, 40, 44, 48, and Week 52)
  • Absolute Change From Baseline for PASI 50 / 75 / 90 / 100 and IGA 2011 Score of 0 or 1 at Week at Week 16, 20, 24,28,32,36,40,44,48,and Week 52(Baseline, week 12,16,20,24,28,32,36,40,44,48 and week 52)
  • Number of Secukinumab Injections Needed to Regain PASI 75 Response From Start of Relapse After Week 12(week 16, 20, 24,28,32,36,40,44,48,and Week 52)
  • Number of Participants Developing Anti-secukinumab Antibodies(Baseline, weeks 12, 24, 52 and 60)
  • Absolute Change From Baseline for PASI 50 / 75 / 90 / 100 and IGA 2011 Score of 0 or 1 at Week 2, 4, 6, 8, 12(Baseline, week 2, 3 , 4, 8, 12)
  • % of Participants Achieving a DLQI Score of 0 or 1 at Each Visit up to Week 52, (Induction)(Baseline to week 2, 4, 6, 8, 12)
  • Median Time to Relapse (Weeks) From Week 12.(Week 12 to week 16, 20, 24, 28, 32, 36, 40, 44, 48, and Week 52.)
  • Percent of Participants Achieving Psoriasis Area & Severity Index (PASI) Score and IGA Mod 2011 0 or 1 Score Over Time at Week 12 and 52 (Induction)(Baseline, week 2, 4, 6, 8, 12)
  • Change From Baseline in Dermatology Life Quality Index (DLQI) Score. up to Week 52, (Induction)(Baseline to week 2, 4, 8, 12)
  • Change From Baseline in EQ-5D at Each Visit, up to Week 52, (Induction)(Baseline to week 2, 4, 8, 12)
  • Change From Baseline in EQ-5D at Each Visit, up to Week 52, (Maintenance)(Baseline to week 16, 20, 24, 28, 32, 36, 40, 44, 48, and Week 52.)
  • Change From Baseline in Dermatology Life Quality Index (DLQI) Score. up to Week 52, (Maintenance)(Baseline to week 16, 20, 24, 28, 32, 36, 40, 44, 48, and Week 52.)
  • Number of Visits With PASI 50, 75, 90, 100 Score and IGA Mod 2011 0 or 1(Week 16, 20, 24,28,32,36,40,44,48,and Week 52)
  • Percent of Responders With PASI Equal to or Greater Than 50, PASI 75, PASI 90, PASI 100 and Percent of Responders With IGA Score of 0 or 1 Who Failed to Respond to a Previous Biologic Psoriasis Therapy(Week 52)

研究者

申办方类型
Industry
责任方
Sponsor

研究点 (1)

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