| City: |
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Baltimore |
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State:
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MD |
| Zip Code: |
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21287 |
| Conditions: |
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Peanut Hypersensitivity - Food Hypersensitivity - Immediate Hypersensitivity |
| Purpose: |
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The purpose of this study is to explore the safety and efficacy of a sublingual (under the
tongue) immunotherapy (SLIT) dosing regimen and an oral immunotherapy (OIT) regimen in
inducing desensitization and long term tolerance in children with persistent peanut allergy.
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| Study summary: |
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To effectively address the Primary Objectives of this pilot study, 30 subjects aged 6-21
years with: (1) a convincing clinical history of PA, (2) a serum IgE specific to peanut of
>0.35 kUa/L and a skin prick test (SPT) wheal >3 mm, will be enrolled. Subjects will be
recruited from the Johns Hopkins Pediatric Allergy Clinic.
Participants will undergo an initial screening visit that will include a medical history,
physical exam, skin testing, and phlebotomy. Informed consent and assent will be obtained.
At the next two visits, 20 participants will complete a double-blind placebo-controlled food
challenge (DBPCFC). Eligible subjects will be randomized in a 1:1 ratio into two groups.
One group will receive active SLIT with placebo OIT and the other group will begin active
OIT with placebo SLIT dose escalation. Over the next 16 weeks of the study, subjects will
undergo SLIT and OIT dose increases. A maintenance dose will then be taken at home daily
for 12 months. A DBPCFC will be completed after 6 months and 12 months of home dosing.
Those patients who pass the DBPCFC will be taken off SLIT and OIT for 4 weeks. A final
challenge will be administered at the end of this period.
Ten additional peanut-allergic subjects age 6-21 years will be enrolled and followed as
longitudinal controls for the mechanistic studies. These subjects will follow a modified
schedule compared to those subjects receiving study treatment and will be evaluated by
phlebotomy, end point titration prick skin testing, and saliva collection. These patients
will continue strict avoidance of peanut unless otherwise advised by their personal
physician. |
| Criteria: |
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Inclusion Criteria:
- Are ages 6 to 21 years of either sex, any race, and any ethnicity at the time of the
initial visit.
- Have a physician diagnosed peanut allergy or a convincing clinical history of peanut
allergy (urticaria, upper or lower respiratory symptoms, GI disturbances, rash or
oral symptoms).
- Have a skin prick test positive to peanut (diameter of wheal 3 mm ≥ negative control)
and detectable serum peanut-specific IgE level (UniCAP ≥ 0.35 kUa/L).
- Have a positive reaction to a cumulative dose of ≤1,000 mg of peanut powder in the
initial qualifying DBPCFC.
- Use an effective method of contraception by females of childbearing potential to
prevent pregnancy and agree to continue to practice an acceptable method of
contraception for the duration of their participation in the study.
- Ability to perform spirometry maneuvers in accordance with the American Thoracic
Society (ATS) guidelines (1994).
- Have self-injectable epinephrine (i.e. EpiPen® or EpiPen Jr.®) available at all
times.
- Provide signed informed consent (by parent or legal guardian if the subject is a
minor) and informed assent if applicable.
Exclusion Criteria:
- Have a history of severe anaphylaxis to peanut with hypoxia (cyanosis or SpO2 ≤92% at
any stage), hypotension or neurological compromise (confusion, collapse, loss of
consciousness or incontinence).
- Tolerates more than 1,000 mg of peanut powder at the initial qualifying DBPCFC.
- Have a viral URI or gastroenteritis within 7 days of OFC (OFC will need to be
rescheduled).
- Currently participating in a study using an investigational new drug.
- Participation in any interventional study for the treatment of food allergy in the
past 12 months.
- Pregnancy or lactation
- Allergy to placebo ingredients (Glycerin or oat flour) OR reacts to any dose of
placebo during the qualifying OFC.
- Currently in a buildup phase of any allergy immunotherapy.
- Poor control of atopic dermatitis.
- Have pulmonary function tests with FEV1 value <80% predicted or any clinical features
of greater than moderate persistent asthma and greater than high daily doses of
inhaled corticosteroids (>500µg/day fluticasone or equivalent).
- Use of steroid medications (oral steroids, such as prednisone or Medrol, steroid
injections, such as Kenalog, or IV or oral corticosteroid burst) in the following
manners:
o History of daily oral steroid dosing within 4 weeks prior to baseline visit or for
> 1 month during the past year or burst oral steroid course in the past 6 months or >
1 burst oral steroid course in the past year.
- Asthma requiring
- ≥1 hospitalization in the past year for asthma or
- >1 ER visit in the past 6 months for asthma
- Use of omalizumab or other non-traditional forms of allergen immunotherapy (e.g.,
oral or sublingual) or immuno-modulatory therapy (not including corticosteroids) or
biologic therapy within the past year.
- Use of β-blockers (oral), angiotensin-converting enzyme (ACE) inhibitors,
angiotensin-receptor blockers (ARB), calcium channel blockers or tricylic
antidepressant therapy.
- Inability to discontinue antihistamines for 5 days for long acting and 3 days for
short acting prior to skin testing or OFC's.
- History of alcohol or drug abuse.
- Active eosinophilic gastrointestinal disease in the past two years.
- Have other significant medical conditions (e.g., liver, gastrointestinal, kidney,
cardiovascular, pulmonary disease, or blood disorders) which, in the opinion of the
Investigator, make the subject unsuitable for induction of food reactions.
- Any previous intubation due to allergies or asthma.
- Severe reaction at initial DBPCFC, defined as:
- Life-threatening anaphylaxis
- Requiring overnight hospitalization |
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| Study is available at: |
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Johns Hopkins University
Baltimore, MD 21287
United States
Primary Contact:
Satya Narisety, MD
Phone: 410-955-5883
Secondary Contact:
Satya Narisety, MD
Phone: 410-955-5883 |
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If you are interested in this clinical trial please use the contact information above. If you would like to get additional information about this clinical trial please visit ClinicalTrials.gov.
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| Data Source: |
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ClinicalTrials.gov |
| Date Processed: |
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March 23, 2011 |
Modifications to
this listing: |
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Only selected fields are shown, please use the link
above to view all information about this clinical trial. |
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