The Use of Exhaled Nitric Oxide as a Predictive Marker of Allergic Reactions to Oral Food Challenge and Clinical Response of Omalizumab Treatment in Subjects With Multiple Food Allergies
概览
- 阶段
- 4 期
- 干预措施
- Omalizumab
- 疾病 / 适应症
- Food Allergy
- 发起方
- AAADRS Clinical Research Center
- 入组人数
- 20
- 试验地点
- 1
- 主要终点
- FeNO change from baseline to week 52
- 状态
- 进行中（未招募）
- 最后更新
- 8个月前
概览
简要总结
This is a Phase IV, open-label, single-center study to evaluate the change in FeNO as a marker of clinical response to OMA in participants with multiple FA.
详细描述
This is a Phase IV, open-label, single-center study to evaluate the change in FeNO as a marker of clinical response to OMA in participants with multiple FA. Twenty (20) participants will be enrolled over a 9-month enrollment period from an allergy and asthma medical specialty clinic. Should the participant meet all eligibility criteria, then following the Screening Period, the participant will be dosed with OMA and asked to continue to follow their food avoidance regimen. Participants will return to the clinic every two weeks for 16-weeks, and then every 2 or 4-weeks (depending on dosing) for the remaining 36-weeks, for a total of 52-weeks. Primary endpoint analyses will occur at Week 16 and Week 52. Description of XOLAIR treatment schedule: Omalizumab will be dosed according to the OUtMATCH Study dosing. Patients will be monitored for acute hypersensitivity reactions for at least 61 minutes after the end of the injection. Epinephrine and parenteral diphenhydramine must be readily available for immediate use if required to treat a hypersensitivity reaction; site personnel must be able to detect and treat such reactions. Patients with severe hypersensitivity reactions (e.g., stridor, angioedema, life-threatening change in vital signs) must be withdrawn from study treatment. All adverse events of systemic hypersensitivity reactions or anaphylactoid or anaphylaxis reactions must be reported within 24 hours to the Sponsor.
研究者
入排标准
入选标准
- •Patients must meet the following criteria for study entry:
- •Able and willing to provide written informed consent from patient and parent or guardian and to comply with the study protocol.
- •Age 6 years of age or older at Visit 1
- •Documented history of food allergy to one or more of the following foods based on SPT performed at baseline visit:
- •tree nuts (Walnut/Pecan, Cashew/Pistachio, Almond, Hazelnut, Brazil nut)
排除标准
- •Patients who meet any of the following criteria will be excluded from study entry:
- •Diagnosis of asthma requiring maintenance medication, including inhaled steroids, leukotriene modifiers, LABA/ICS, biologics medications (Intermittent asthma \[Step 1\] is allowed and defined according to the 2020 NAEPP guidelines (as 'asthma requiring only prn SABA use) and FEV1 \< 80% of predicted normal.
- •Diagnosis of nasal polyps, cystic fibrosis or any respiratory condition that will skew normally occurring FeNO levels
- •FeNO (measured in ppb) is lower than a value expected for the age, height, and gender of the participant or inability to perform respiratory collection maneuver
- •Systemic steroids, leukotriene modifiers, or nasal steroids for any cause/diagnosis within 4 weeks of baseline
- •Biologic use, for any diagnosis, within five half-lives of Screening
- •Antibiotic use, systemic/oral/intramuscular, for any cause/diagnosis within 2 weeks of baseline
- •Active smoker, cigarette, cigar, vape, recreational, and/or prior 10 pack year history
- •Participant weight or IgE levels outside of the dosing table for OMA
- •Known history of anaphylaxis/hypersensitivity to OMA
研究组 & 干预措施
Open Label Injection of Omalizumab
Omalizumab dose and frequency based on baseline patient weight and total IgE
干预措施: Omalizumab
结局指标
主要结局
FeNO change from baseline to week 52
时间窗: 1 year
biomarker
次要结局
- Time to change from baseline FeNO during OFC(at baseline and at week 16)