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Safety Study of Viaskin Peanut to Treat Peanut Allergy
Not Recruiting
Trial ID: NCT02916446
Purpose
This study evaluates the safety of Viaskin Peanut 250 mcg in the treatment of peanut allergy in children from 4 to 11 years of age. Subjects will receive either Viaskin Peanut 250 mcg or a placebo for a period of 6 months, after which all subjects will be receiving the active treatment up to a period of 3 years under active treatment.
Stanford Investigator(s)
Sayantani Sindher
Clinical Associate Professor, Medicine Clinical Associate Professor, Pediatrics - Allergy and Clinical Immunology
R. Sharon Chinthrajah
Associate Professor of Medicine (Sean Parker Center) and of Pediatrics (Allergy and Clinical Immunology)
Eligibility
Inclusion Criteria:
* Physician-diagnosed peanut allergy;
* A peanut Skin Prick Test (SPT) with a wheal largest diameter ≥8 mm;
* A specific-peanut Immunoglobulin E (IgE) ≥14 kU/L;
* Subjects following a strict peanut-free diet.
Exclusion Criteria:
* Generalized dermatologic disease
* Spirometry forced expiratory volume in 1 second (FEV1) \<80% of the predicted value, or peak expiratory flow (PEF) \<80% of predicted value;
* Receiving β-blocking agents, angiotensin-converting enzyme inhibitors, angiotensin-receptor blockers, calcium channel blockers or tricyclic antidepressant therapy; anti-tumor necrosis factor drugs or anti-IgE drugs (such as omalizumab) or any biologic immunomodulatory therapy;
* Prior or concomitant history of any immunotherapy to any food allergy (for example EPIT, OIT, SLIT, or specific oral tolerance induction).
Intervention(s):
biological: Viaskin Peanut 250 mcg
biological: Placebo
Not Recruiting
Contact Information
Stanford University
School of Medicine
300 Pasteur Drive
Stanford,
CA
94305
Sharon Chinthrajah, MD
6505217237