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A Randomized, Double-Blind, Placebo-Controlled Pilot Study of Sublingual/Oral Immunotherapy for the Treatment of Peanut Allergy

This study has been completed.
Information provided by (Responsible Party):
Robert A. Wood, Johns Hopkins University Identifier:
First received: March 8, 2010
Last updated: March 28, 2016
Last verified: March 2016

March 8, 2010
March 28, 2016
March 2010
January 2012   (Final data collection date for primary outcome measure)
The primary endpoint is to determine if sublingual administration of peanut extract and oral administration of peanut powder can induce a 10-fold increase in tolerance as measured by food challenge. [ Time Frame: 1 1/2 years ]
Same as current
Complete list of historical versions of study NCT01084174 on Archive Site
  • The incidence of all serious adverse events on peanut SLIT and peanut OIT. [ Time Frame: 1 1/2 years ]
  • To assess any changes in clinical and mechanistic endpoints. [ Time Frame: 1 1/2 years ]
  • Peanut tolerance, as determined by oral food challenge (OFC) after being off daily SLIT and OIT for 4 weeks. [ Time Frame: 1 1/2 years ]
Same as current
Not Provided
Not Provided
A Randomized, Double-Blind, Placebo-Controlled Pilot Study of Sublingual/Oral Immunotherapy for the Treatment of Peanut Allergy
A Randomized, Double-Blind, Placebo-Controlled Pilot Study of Sublingual/Oral Immunotherapy for the Treatment of Peanut Allergy
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.

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.

Phase 1
Phase 2
Allocation: Randomized
Intervention Model: Parallel Assignment
Masking: Double Blind (Subject, Caregiver, Investigator, Outcomes Assessor)
Primary Purpose: Treatment
  • Peanut Hypersensitivity
  • Food Hypersensitivity
  • Immediate Hypersensitivity
  • Drug: Peanut powder
    Delivered orally
  • Drug: Peanut extract
    Delivered sublingually
  • Drug: Placebo extract
    Delivered sublingually
  • Drug: Placebo powder
    Delivered orally
  • Experimental: 1
    These subjects will receive peanut powder given orally and placebo extract given sublingually.
    • Drug: Peanut powder
    • Drug: Placebo extract
  • Experimental: 2
    These subjects will receive peanut extract given sublingually and placebo powder given orally.
    • Drug: Peanut extract
    • Drug: Placebo powder
Not Provided

*   Includes publications given by the data provider as well as publications identified by Identifier (NCT Number) in Medline.
January 2013
January 2012   (Final data collection date for primary outcome measure)

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
Sexes Eligible for Study: All
6 Years to 21 Years   (Child, Adult)
Contact information is only displayed when the study is recruiting subjects
United States
Not Provided
Not Provided
Robert A. Wood, Johns Hopkins University
Johns Hopkins University
Not Provided
Principal Investigator: Robert Wood, MD Johns Hopkins University
Johns Hopkins University
March 2016

ICMJE     Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP