Trial Search Results
Efficacy and Safety of Several Doses of Viaskin Peanut in Adults and Children With Peanut Allergy
The objectives of this dose-finding study for the treatment of peanut allergy are:
- To determine the efficacy of 3 doses of Viaskin Peanut (50 mcg ,100 mcg and 250 mcg peanut protein per patch) to significantly desensitize peanut-allergic subjects to peanut after 12 months of treatment.
- To evaluate the safety of a long-term treatment with Viaskin Peanut.
Stanford is currently not accepting patients for this trial.
- Biological: Viaskin Peanut 50 mcg
- Biological: Viaskin Peanut 100 mcg
- Biological: Viaskin Peanut 250 mcg
- Biological: Viaskin Placebo
- Peanut-allergic subjects between 6 and 55 years of age, with a well-documented medical
history of systemic reactions after ingestion of peanut and currently following a
strict peanut-free diet.
- Peanut-specific immunoglobulin E (IgE) level (Phadia CAP-system) > 0.7 kU/L and a
positive skin prick test to peanut with a largest wheal diameter ≥ 8 mm
- Positive double-blind placebo-controlled food challenge (DBPCFC) at ≤ 300 mg of peanut
proteins: the eliciting dose of peanut proteins during the DBPCFC is capped at 300 mg,
i.e. subjects must react to peanut before reaching or at the dose of 300 mg peanut
- Negative pregnancy test for women of childbearing potential. Females of childbearing
age must use effective methods of contraception to prevent pregnancy and agree to
continue to practice an acceptable method of contraception for the duration of
participation in the study. Sexual abstinence will be accepted as an effective method
of contraception for girls below 15 years of age.
- Ability to perform spirometry maneuvers in accordance with the American Thoracic
Society guidelines (2005) for subjects 9 years of age and above Subjects below 9 years
of age can perform peak expiratory flow (PEF) instead.
- Willing to comply with all study requirements during their participation in the study.
- Provide signed informed consent and assent as appropriate.
- Subjects with a history of severe anaphylaxis to peanut with the following symptoms:
hypotension, hypoxia, neurological compromise (collapse, loss of consciousness or
- Pregnancy or lactation.
- FEV1 <80% of the predicted value at screening for subjects 9 years of age and above.
PEF < 80% of predicted for subjects below 9 years of age.
- Subjects who did not react at or below the dose of 300 mg of peanut proteins during
the DBPCFC at screening.
- Known allergy or known hypersensitivity to placebo excipients either of the Viaskin
patches or of the food challenge formulas.
- Subjects reacting objectively to the placebo formula at screening.
- Severe reaction during the screening food challenge, defined as need for intubation,
hypotension persisting after epinephrine administration, or the need for more than two
doses of epinephrine.
- Inability to discontinue short-acting antihistamines for three days or long-acting
antihistamines for five to seven days (depending on half-life) prior to skin prick
testing or food challenges.
- Subjects treated with systemic long-acting corticosteroids (depot corticosteroids)
within 12 weeks prior to the screening visit and/or systemic short-acting
corticosteroid within 4 weeks prior to the screening visit or any systemic
corticosteroid at screening.
- Subjects with asthma defined as follows:
1. uncontrolled persistent asthma by National Asthma Education and Prevention
Program Asthma guidelines (2007) or by Global Initiative for Asthma (2011) or
being treated with combination therapy of medium dose inhaled corticosteroid with
a long acting inhaled β2-agonists;
2. at least two systemic corticosteroid courses for asthma in the past year or one
oral corticosteroid course for asthma in the past three months;
3. prior intubation for asthma in the past two years.
- Subjects on β-blocking agents, angiotensin-converting enzyme inhibitors,
angiotensin-receptor blockers, calcium channel blockers or tricyclic antidepressant
- Subjects undergoing any type of immunotherapy to any food within one year prior to the
- Subjects presently on aeroallergen immunotherapy and unwilling or unable to
- Subjects currently treated with anti-tumor necrosis factor drugs or anti-IgE drugs
(such as omalizumab) or any biologic immunomodulatory therapy within one year prior to
the screening visit.
- Allergy or known history of reaction to Tegaderm®.
- Subjects suffering from generalized dermatologic diseases (e.g. severe atopic
dermatitis, uncontrolled generalized eczema, keratosis pilaris, ichthyosis vulgaris)
with no intact skin zones to apply the patches.
- Any disorder in which epinephrine is contraindicated such as coronary artery disease,
uncontrolled hypertension, or serious ventricular arrhythmias.
- Participation in another clinical intervention study in the three months prior to the
- Subjects on any experimental drugs or treatments.
Other inclusion/exclusion criteria may apply.
Ages Eligible for Study
6 Years - 55 Years
Genders Eligible for Study