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临床试验/NL-OMON45596
NL-OMON45596已完成3 期

A randomized, double-blind, active control, multicenter study to evaluate the efficacy at week 52 of subcutaneously administered secukinumab monotherapy compared with subcutaneously administered adalimumab monotherapy in patients with active psoriatic arthritis - CAIN457F2366 (EXCEED 1)

ovartis0 个研究点目标入组 15 人开始时间: 待定最近更新:
适应症

试验速览

阶段
3 期
状态
已完成
发起方
ovartis
入组人数
15

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 99(—)

入选标准

  • Diagnosis of PsA classified by CASPAR; Rheumatoid factor and anti-CCP antibodies negative; diagnosis of active plaque psoriasis, with at least one psoriatic plaque of *2cm diameter or nail changes consistent with psoriasis or documented history of plaque psoriasis; inadequate control of symptoms with NSAIDs; inadequate control of symptoms with a conventional DMARD.;Other protocol-defined inclusion criteria may apply. See protocol for more details.

排除标准

  • Pregnant or nursing women, evidence of ongoing infectious or malignant process; previous exposure to any biologic drug for Psoriatic Arthritis or Psoriasis; subjects taking high potency opioid analgesics; ongoing use of prohibited psoriasis treatments / medications; previous treatment with any cell-depleting therapies including but not limited to anti-CD20, investigational agents;Other protocol-defined exclusion criteria may apply. See protocol for more details.

研究者

发起方
ovartis

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