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临床试验/NCT04222491
NCT04222491Enrolling By Invitation2 期

Outcomes of Clinical Food Oral Immunotherapy for Peanut Allergy

Massachusetts General Hospital1 个研究点 分布在 1 个国家目标入组 500 人开始时间: 2020年6月25日最近更新:
适应症
干预措施
相关药物

试验速览

阶段
2 期
状态
Enrolling By Invitation
入组人数
500
试验地点
1
主要终点
The proportion of participants who tolerate the maintenance dose of 300 mg peanut protein with no symptoms within two years of starting OIT

研究概览

简要总结

This is an open label observational single center study of clinical food oral immunotherapy outcomes with biomarker samples and participant and/or caregiver-completed questionnaires in participants between 6 months and 65 years of age with IgE-mediated peanut allergy undergoing food oral immunotherapy.

详细描述

In this research study the investigators want to learn more about the experience of participants with peanut allergy and their caregivers undergoing food oral immunotherapy (OIT) for peanut allergy. Food oral immunotherapy (OIT) is a treatment for individuals with a food allergy to reduce the body's allergic response to the food allergen, resulting in fewer symptoms. The treatment is also called desensitization. An individual becomes desensitized to the food allergen by ingesting small amounts of the food that are slowly increased. Over time, this helps the body's immune system become used to the food so that it no longer causes an allergic reaction. By desensitizing to peanut, it may lower the risk of life-threatening allergic reactions and cause a decreased sensitivity to peanut. The investigators specifically want to learn more about the effects of food OIT on quality of life and other outcomes important to participants with peanut allergy and their caregivers and to ultimately develop tests to predict who may respond favorably to food OIT.

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
主要目的
Treatment
盲法
None

入排标准

年龄范围
6 Months 至 65 Years(Child, Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Individuals between 6 months and 65 years of age with a diagnosis of immunoglobulin E (IgE)-mediated peanut allergy and their caregivers; a diagnosis of IgE-mediated peanut allergy is defined by: (1) documented history of peanut allergy or determined to be allergic by oral food challenge; (2) evidence of peanut-specific IgE by either: positive skin prick test to peanut allergen (reaction wheal at least 3 mm larger than saline control) or serum peanut-specific IgE > 0.34 kilo-unit/liter (kU/L) or international unit/milliliter (IU/mL) at screening visit
  • Referral by Massachusetts General Hospital (MGH) allergist for food oral immunotherapy
  • Willing to sign informed consent or whose caregiver is willing to sign the informed consent (age appropriate)
  • Willing to sign the assent form, if age appropriate

排除标准

  • History of severe or life-threatening episode of anaphylaxis or anaphylactic shock within 60 days of screening
  • Severe or poorly controlled asthma
  • Diagnosis of other severe or complicating medical problems, including autoimmune or chronic immune inflammatory conditions or gastrointestinal inflammatory conditions, such as inflammatory bowel diseases and eosinophilic gastrointestinal disorders
  • Current use of beta blocker medication(s)
  • Inability to cooperate with and/or perform oral food challenge procedures
  • Females who are pregnant, planning to become pregnant, or breastfeeding
  • Investigator determination of safety concern for any reason

研究组 & 干预措施

active peanut OIT

Experimental

active peanut oral immunotherapy

干预措施: Peanut oral immunotherapy (Drug)

结局指标

主要结局

The proportion of participants who tolerate the maintenance dose of 300 mg peanut protein with no symptoms within two years of starting OIT

时间窗: 2 years

Feasibility analysis as assessed by the proportion of participants who tolerate the maintenance dose in a dichotomous manner

次要结局

  • Change in skin prick test reactivity to peanut extract from baseline to end of treatment(4 years)
  • Change in quality of life scores from baseline to end of treatment(4 years)
  • Number of participants with treatment-related adverse events as assessed by CTCAE v4.0(4 years)
  • Change in peanut specific serum immunoglobulin E (IgE) from baseline to end of treatment(4 years)
  • The proportion of participants who tolerate a cumulative dose of 5000 mg peanut protein on oral food challenge without treatment after 12 months on maintenance dose(4 years)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Wayne G. Shreffler, MD, PhD

Principal Investigator

Massachusetts General Hospital

研究点 (1)

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