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临床试验/EUCTR2018-000993-31-SK
EUCTR2018-000993-31-SK进行中(未招募)1 期

A multicenter, randomized, double-blind, placebo- controlled phase 2b dose-finding study to investigate the efficacy, safety and tolerability of LOU064 in adult chronic spontaneous urticaria patients inadequately controlled by H1-antihistamines

ovartis Pharma AG0 个研究点目标入组 308 人开始时间: 2019年3月25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
308

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

性别
All

入选标准

  • 1. Signed informed consent must be obtained prior to participation in the study
  • 2. Male and female subjects aged =18 years of age
  • 3. CSU diagnosis for = 6 months prior to screening
  • 4. Diagnosis of CSU inadequately controlled by second generation H1-antihistamines at the time of randomization as defined in the following:
  • - The presence of itch and hives for =6 consecutive weeks prior to screening in spite of use of non-sedating H1-antihistamines according to local treatment guidelines during this time period
  • - UAS7 score (range 0-42) =16 and HSS7 score (range 0-21) = 8 during 7 days prior to randomization (Day 1)
  • 5. Willing and able to complete an Urticaria Participant Daily eDiary (UPDD) for the duration of the study
  • 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 286
  • F.1.3 Elderly (>=65 years) yes
  • F.1.3.1 Number of subjects for this age range 22

排除标准

  • 1. Hypersensitivity to any of the study treatments
  • 2. Clearly defined, predominant or sole trigger of their chronic urticaria (chronic inducible urticaria)
  • 3. Other diseases with symptoms of urticaria or angioedema
  • 4. Other skin disease associated with chronic itching that might influence in the investigators opinion the study evaluations and results
  • 5. Known or suspected history of an ongoing, chronic or recurrent infectious disease
  • including but not limited to opportunistic infections (eg tuberculosis, atypical
  • mycobacterioses, listeriosis or aspergillosis), HIV, Hepatitis B/C.
  • 6. Pregnant or nursing (lactating) women
  • 7. Women of child-bearing potential not using highly effective methods of contraception
  • Other protocol-defined exclusion criteria may apply

研究者

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Dose-finding study to evaluate efficacy and safety... | 临床试验