Healia Clinical Trials Information Database

Oral Immunotherapy for Peanut Allergy

Peanut allergy is known to cause severe anaphylactic reactions.The goal of this proposal is to produce a new treatment that would benefit subjects who have peanut allergy by lowering the risk of anaphylactic reactions (desensitization), and changing the peanut-specific immune response in subjects who have peanut allergy (tolerance).

Description

Peanut allergy is known to cause severe anaphylactic reactions. Compared with other food allergies it tends to be more persistent and also its prevalence seems to be rising. Currently there is no proven treatment other than strict avoidance. We are attempting to decrease the risk of anaphylaxis on accidental ingestion by desensitizing subjects to peanut using peanut oral immunotherapy (OIT). We are also studying the effect of peanut OIT on the peanut specific immune response to determine if tolerance to peanut protein will develop. Children ages one to six years of age with peanut allergy will be randomized to peanut OIT or placebo (active subjects). Thirty subjects will also be recruited as controls. These subjects will not receive any peanut or placebo but only have skin prick testing and lab work in addition to a history and physical exam. Active subjects will undergo a modified rush immunotherapy on the first day and then increase the doses at least every two weeks up to a maintenance dose of 4 grams (equivalent to about 13 peanuts). Doses will be taken daily at home except for dose increases which will be done on the DCRU. Outcome variables of interest include response to double-blind placebo controlled food challenge, skin prick testing, peanut specific IgE, and adverse events. These results will be compared between the start and end of peanut OIT using appropriate statistical analysis.

Status: Recruiting (Phase 2). Started on June 1st, 2009.

Enrollment: 60 subjects

Study Type: Interventional

Study Design:

  • Allocation: Randomized
  • Endpoint Classification: Safety/Efficacy Study
  • Intervention Model: Crossover Assignment
  • Masking: Double Blind (Subject
  • Caregiver
  • Investigator)
  • Primary Purpose: Treatment

Conditions:

Interventions:

  • Other: Peanut flour
  • Other: Subjects will receive oral oat flour.

Eligibility

Inclusion Criteria:

  • Age 1- 6 years all of either sex, any race, any ethnicity at the time of the initial visit

  • The presence of IgE specific to peanuts (a positive skin prick test to peanuts (diameter of wheal >3.0 mm) and a positive in vitro IgE [CAP-FEIA] > 7 kUA/L

  • A history of significant clinical symptoms occurring within 60 minutes after ingesting peanuts

  • Provide signed informed consent

Exclusion Criteria:

  • History of severe anaphylaxis to peanut as defined by hypoxia, hypotension, or neurological compromise (Cyanosis or SpO2 < 92% at any stage, hypotension, confusion, collapse, loss of consciousness; or incontinence)

  • 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

  • Subjects with a known wheat food allergy will be excluded because of cross contamination of oat with wheat

  • Poor control or persistent activation of atopic dermatitis

  • Moderate to severe persistent asthma

  • Currently being treated with greater than medium daily doses of inhaled corticosteroids, as defined by the NHLBI guidelines

  • Inability to discontinue antihistamines for skin testing and OFCs

Gender

Both

Mininum Age

1 Year

Maximum Age

6 Years

Healthy Volunteers

No


Resources

Source: Duke University

Authority: United States: Institutional Review Board

Locations

  • Duke University Medical Center
    Durham
    North Carolina
    27710
    United States

Officials

  • Wesley Burks, MD (Principal Investigator, Duke University)

Sponsors

  • Duke University (Lead Sponsor)

References

  • Patriarca G, Nucera E, Roncallo C, Pollastrini E, Bartolozzi F, De Pasquale T, Buonomo A, Gasbarrini G, Di Campli C, Schiavino D. Oral desensitizing treatment in food allergy: clinical and immunological results. Aliment Pharmacol Ther. 2003 Feb;17(3):459-65. Erratum in: Aliment Pharmacol Ther. 2003 May 1;17(9):1205.
    PMID: 12562461.
    Check for Full Text

  • Buchanan AD, Green TD, Jones SM, Scurlock AM, Christie L, Althage KA, Steele PH, Pons L, Helm RM, Lee LA, Burks AW. Egg oral immunotherapy in nonanaphylactic children with egg allergy. J Allergy Clin Immunol. 2007 Jan;119(1):199-205. Epub 2006 Oct 27.
    PMID: 17208602.
    Check for Full Text

Links

None.


Date Verified
June 1st, 2010
First Received
June 17th, 2010
Last Changed
June 17th, 2010

Information obtained from ClinicalTrials.gov on June 09, 2011. Link to the current ClinicalTrials.gov record.


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The Healia Clinical Trials Search Engine searches the data set at clinicaltrials.gov, providing up-to-date information about current clinical trials. In the Healia Clinical Trials Database you can find information on new experimental drugs, medical devices, and other types of treatments for all types of diseases. Each clinical trial description includes information about the phase of the trial (phase I, phase II, or phase III), the trial’s methods, such as whether it is a randomized, placebo controlled, double blind study, and the status of the trial including whether or not the trial is currently enrolling new participants.


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