EUCTR2018-000326-58-SE
Active, not recruiting
Phase 1
Peanut Allergy Oral Immunotherapy Study of AR101 for Desensitization in Children and Adolescents: Real-World, Open-Label, Quality of Life Study - Quality of Life study of AR101 CODIT
Overview
- Phase
- Phase 1
- Status
- Active, not recruiting
- Sponsor
- Aimmune Therapeutics, Inc.
- Enrollment
- 200
Overview
Brief Summary
No summary available.
Study Design
- Study Type
- Interventional clinical trial of medicinal product
Eligibility Criteria
Inclusion Criteria
- •1\. Aged 4 to 17 years, inclusive, at screening
- •2\. Written informed consent from subjects, as appropriate per local requirements, and legal
- •guardian/parent (or both parents where required by local authorities) of subjects who are
- •3\. Written assent from subjects who are minors, as appropriate per local requirements
- •4\. Written informed consent from the parent/caregiver who will complete relevant questionnaires during the study
- •5\. History of physician\-diagnosed immunoglobulin (Ig) E\-mediated peanut allergy that includes the onset of characteristic signs and symptoms of allergy within 2 hours of known oral exposure to peanut or peanut\-containing food. In general, characteristic signs and symptoms of IgE\-mediated allergic reactions are objective and affect the target organs of skin, gastrointestinal (GI) tract, upper/lower respiratory tract, cardiovascular system, or a combination of target organs
- •6\. Mean wheal diameter on SPT to peanut \= 8 mm greater than the negative saline control at screening
- •7\. Serum IgE to peanut of \= 14 kUA/L at screening
- •8\. For sexually active females of childbearing potential, use of a highly effective method of birth control, defined as one that results in a low failure rate (ie, \< 1% per year) when used consistently and correctly
- •Are the trial subjects under 18? yes
Exclusion Criteria
- •1\. Uncertain clinical diagnosis of peanut allergy
- •2\. History of severe or life\-threatening anaphylaxis or anaphylactic shock within 60 days before screening
- •3\. History of eosinophilic esophagitis (EoE); other eosinophilic GI disease; chronic, recurrent, or severe gastroesophageal reflux disease (GERD); symptoms of dysphagia (eg, difficulty swallowing, food getting stuck”); or recurrent GI symptoms of any etiology
- •4\. History of a mast cell disorder including systemic mastocytosis, urticaria pigmentosa, chronic idiopathic or chronic physical urticaria beyond simple dermatographism (eg, cold urticaria, cholinergic urticaria), and hereditary or idiopathic angioedema
- •5\. Severe persistent asthma
- •6\. Mild or moderate asthma (criteria steps 1\-4; NHLBI, 2007\) that is uncontrolled or difficult to control
- •7\. History of high\-dose corticosteroid medication use (eg, \> 3 days at 1\-2 mg/kg of prednisone or equivalent)
- •8\. History of chronic disease (except asthma, atopic dermatitis, or allergic rhinitis) that is or is at significant risk of becoming unstable or requiring a change in a chronic therapeutic regimen, including malignancies within 5 years before screening and autoimmune diseases
- •9\. History of cardiovascular disease including uncontrolled or inadequately controlled hypertension
- •10\. Use of beta\-blockers (oral), angiotensin\-converting enzyme inhibitors, angiotensin receptor blockers, calcium channel blockers, or tricyclic antidepressants
Investigators
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