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临床试验/EUCTR2016-000972-91-SK
EUCTR2016-000972-91-SK进行中(未招募)1 期

A randomized, double-blind, placebo-controlled multicenter study of subcutaneous secukinumab to demonstrate efficacy in the treatment of enthesitis at the Achilles tendon up to 1 year in adult patients with active Psoriatic Arthritis (PsA) and axial Spondyloarthritis (axSpA) (ACHILLES) - ACHILLES

ovartis Pharma Services AG0 个研究点目标入组 200 人开始时间: 2016年7月20日最近更新:
适应症
相关药物

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 clinical trial of medicinal product

入排标准

入选标准

  • - Psoriatic arthritis patients must fulfill the following criteria:
  • Diagnosis of Psoriatic arthritis classified by Classification criteria for Psoriatic Arthritis (CASPAR criteria) with symptoms for at least 6 months and active Psoriatic arthritis as assessed by > 1 tender joints out of 78 and > 1 swollen joints out of 76 at Baseline (dactylitis of a digit counts as one joint each)
  • - Axial Spondyloarthritis patients must fulfill the following criteria:
  • Axial Spondyloarthritis as per the classification of the Assessment of Spondyloarthritis International Society axial Spondyloarthritis (ASAS) criteria with objective signs of inflammation at Screening (magnetic resonance imaging (MRI) with Sacroiliac joint inflammation or definite radiographic sacroilitis according to the modified New York (NY) criteria and/or abnormal high sensitivity C-Reactive Protein (hsCRP)) and active disease assessed by total Bath ankylosing spondylitis disease activity index (BASDAI) = 4 (0–10) at Baseline
  • - Diagnosis of Achilles tendon enthesitis according to swelling and tenderness at the insertional site of the Achilles tendon into the calcaneus
  • - Onset of heel pain = 1 month up to 5 years at Baseline
  • - Heel enthesitis that is magnetic resonance imaging (MRI)-positive according to the investigator`s judgement
  • - Patients who are Tumor necrosis factor (TNF) inhibitor-naive
  • Other protocol defined inclusion criteria may apply.
  • Are the trial subjects under 18? no
  • Number of subjects for this age range:
  • F.1.2 Adults (18-64 years) yes
  • F.1.2.1 Number of subjects for this age range 180
  • F.1.3 Elderly (>=65 years) yes
  • F.1.3.1 Number of subjects for this age range 20

排除标准

  • - Chest X-ray or chest magnetic resonance imaging (MRI) with evidence of ongoing infectious or malignant process
  • - Previous exposure to secukinumab or other biologic drug directly targeting Interleukin (IL)-17 or Interleukin (IL)-17 receptor
  • - Ongoing use of psoriasis treatments / medications (e.g. topical corticosteroids, ultraviolet (UV) therapy) at randomization
  • - Patients who have previously been treated with Tumor necrosis factor (TNF) inhibitors (investigational or approved).
  • - Patients who have ever received biologic immunomodulating agents (investigational or approved)
  • - Pregnant or nursing (lactating) women
  • - History of ongoing, chronic or recurrent infectious disease or evidence of tuberculosis infection
  • Other protocol defined exclusion criteria may apply.

研究者

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