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临床试验/NCT01056783
NCT01056783已完成2 期

A Randomized, Placebo-controlled, Double-blind, Single-centre Proof-of-concept Study of OC000459 in Adult Patients With Active Eosinophilic Esophagitis

Oxagen Ltd1 个研究点 分布在 1 个国家目标入组 26 人开始时间: 2010年8月最近更新:
适应症
干预措施
相关药物

试验速览

阶段
2 期
状态
已完成
发起方
Oxagen Ltd
入组人数
26
试验地点
1
主要终点
Effect of OC000459 on eosinophil load of the esophageal tissue

研究概览

简要总结

This will be a randomised, double blind, placebo controlled, parallel group evaluation of the effect of OC000459 given orally for eight weeks on active eosinophilic esophagitis.

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 75 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Previously diagnosed and symptomatic isolated eosinophilic esophagitis.
  • Relevant eosinophil tissue inflammation as demonstrated by a mean eosinophil load >= 20 eos/hpf in 8 biopsies at the baseline visit.
  • Able to swallow placebo medication successfully under supervision in the clinic
  • Free of all medications for EoE (including topical steroids) for at least 2 weeks prior to baseline and free of systemic steroids for at least 90 days before screening. A proton-pump inhibitor is allowed if required for treatment of secondary acid reflux.

排除标准

  • Other causes of esophagitis (GERD, peptic ulceration, infection etc.)
  • Other causes of eosphagaeal or generalized eosinophilia (i.e. hypereosinophilic syndromes, parasitic infection, GERD)
  • The patient's EoE is dependant on the level of seasonal allergens and the patient's participation in the study will occur during the allergy season.
  • History of abnormal gastric or duodenal eosinophilia (e.g. HES, Churg Strauss vasculitis, EG or a parasitic infection)
  • Receipt of forbidden prescribed or over the counter medication within the 4 weeks prior to the baseline visit and for the duration of the trial, including vitamins and herbal remedies.

研究组 & 干预措施

OC000459

Experimental

OC000459 100mg twice daily

干预措施: OC000459 (Drug)

Placebo

Placebo Comparator

干预措施: Placebo (Drug)

结局指标

主要结局

Effect of OC000459 on eosinophil load of the esophageal tissue

时间窗: 8 weeks

次要结局

  • Effect of OC000459 on EoE related blood and tissue biomarkers(8 weeks)
  • Effect of OC000459 on clinical manifestations of EoE(8 weeks)
  • Effect of OC000459 on endoscopic alterations(8 weeks)
  • Safety and tolerability of OC000459 in patients with active EoE(8 weeks)

研究者

发起方
Oxagen Ltd
申办方类型
Industry
责任方
Sponsor

研究点 (1)

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