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Trichuris Suis Ova in Peanut Allergy - NCT01070498-02215(Clinical Trial 562261)



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City:  Boston
State:  
MA
Zip Code: 02215
Conditions: Peanut Allergy
Purpose: The goal of this study is to determine whether Trichuris suis ova, a potential immunomodulator, is safe in adults and children allergic to peanut.
Study summary: Food allergy is a major cause of life-threatening hypersensitivity reactions. Currently avoidance of the allergenic food is the only established method of preventing reactions in allergic patients. This situation impacts significantly the lives of patients, mainly children, and their families. The current increase in the prevalence of allergic diseases, food allergy in particular, in the Western world has been attributed in part to changes in life style. Before the mid 20th century individuals were exposed to numerous bacterial, parasitic and viral agents. Since these times the progress of hygiene has considerably reduced the risk of exposure to these agents. It is thought that this lack of exposure, particularly during childhood, has led to subtile changes in humans' immune system resulting in an increased propensity to develop allergic and autoimmune responses, the so-called hygiene hypothesis. One of the means of reverting this propensity could be exposure to harmless biological agents. One such agent, eggs of the parasite Trichuris suis (Trichuris suis ova, TSO), has been shown to be well tolerated and efficient in patients with inflammatory bowel diseases. This phase I study will assess whether TSO is safe in adults and children with peanut allergy.
Criteria: Inclusion Criteria: - 18 to 64 years old - Presence of specific IgE (peanut IgE> 7kU/L) to peanuts, positive skin-prick test to peanut and a history of significant clinical symptoms within 60 minutes after the ingestion of peanuts. - Peanut allergy of mild to moderate grade based on the presence of localized or generalized erythema/urticaria/angioedema/oral pruritis, gastrointestinal symptoms, rhinoconjunctivitis, or mild laryngeal edema (voice change/tightening of throat/mild asthma), and the absence of symptoms/signs of severity (marked dyspnea, hypoxia, cyanosis, hypotension, confusion, incontinence, collapse or loss of consciousness) - Otherwise in good health - Ability to provide written 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, confusion, collapse, loss of consciousness, or incontinence) - Poor control or persistent activation of atopic dermatitis - Inability to discontinue antihistaminic for skin testing - Severe persistent asthma as defined by the NHLBI criteria - Asthma that requires oral steroids - Asthma that has been controlled for less than 1 year - FEV1<80% at the screening visit or immediately before the 1st administration of TSO - Currently being treated with greater than medium daily doses of inhaled corticosteroids, as defined by the NHLBI guidelines - Abnormal blood cell count - Abnormal renal function (creatinine above twice the upper limit of normal range) - Abnormal hepatic tests (AST, ALT above twice the upper limit of normal range) - Allergy to Trichuris species - Currently treated with anti-helminthic medication - Previous treatment with immunosuppressive therapy, cytotoxic chemotherapy or lymphoid irradiation for any reason - Insulin dependent diabetes - History of HIV-1, HTLV-1 or Lyme disease - Significant physical or mental disease that would preclude successful compliance and participation in the study, or, in the opinion of the investigators, constitute a hazard, such that enrollment in the study would not be in the subject's best interest - Presence or history of cancer of any type except successfully treated basal cell or squamous cell carcinoma of the skin - History of alcohol or drug abuse in the last 12 months; chronic liver or biliary disease - Pregnancy and lactation; women of child bearing potential must have a documented negative pregnancy test at entry and at each visit during the study, and must be willing to practice adequate birth control during the duration of the study - History of parasitism or positive stool determination for ova or parasite at screening - Unwillingness or inability of patients (or caregivers) to give written consent or to follow the protocol successfully, including coming to the clinic every 2 weeks for about 4 months - Currently participating in a study using an investigational new drug - Participation in any interventional study for the treatment of food allergy in the past 6 months - Presence in the household of an immunodeficient or immunosuppressed individual
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Data Source: ClinicalTrials.gov
Date Processed: January 6, 2011
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