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Completed

NCT Number: NCT01162473

Milk Oral Immunotherapy in Children to Treat Food Allergy

Background and Rationale

For patients with Immunoglobulin E (IgE)-mediated food allergy, the current management includes identification of the causative food and avoidance. Specifically, among young children, cow's milk allergy is the most common food allergy, occurring in as many as 2-3%. Given the prevalence of milk and the difficulty to avoid it in the diet, the investigators aim to investigate the safety and efficacy of oral immunotherapy for cow's milk allergy.

Main Objective

The primary objective is to study the efficacy of milk oral immunotherapy.

Target Population

Children aged six to 17 years with a history of cow's milk allergy will be recruited from The Children's Hospital of Philadelphia Allergy clinical offices for the investigators study.

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Key information

Age range

6 year–17 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Early Phase 1

Primary location

The Children's Hospital of Philadelphia

Philadelphia, Pennsylvania, 19104, United States

About this study

Primary Study Interventions

Prior to and after the desensitization, we will conduct double-blind placebo controlled food challenges to cow's milk protein. During the desensitization phase, we will give increasing doses of cow's milk protein by mouth on a weekly basis, as tolerated. The desensitization protocol starts with dilutional doses of milk and build up to a goal of 8 ounces of cow's milk.

Main Study Outcome Measure

The percentage of children completing the desensitization protocol in each study group will be the primary outcome measure.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Subjects must be age six to 17 years and have a history of cow's milk allergy. Subjects shall maintain strict avoidance of consumption of all cow's milk protein containing foods.
  • Subjects will have a history (within the past six months) of a positive skin prick test to milk extract or an immunocap IgE level greater than 0.35 kilounits per liter (kU/L), and a positive allergic reaction history to milk within the past 12 months.
  • Subjects must be in good health, as determined by medical history and physical examination performed by a study physician.
  • Females of childbearing potential must be using an effective method of contraception, including abstinence, and agree to continue to practice an acceptable method of contraception for the duration of their participation in the study.
  • Informed consent of parent or legal guardian is required.

Exclusion criteria

  • Ability to tolerate eight ounces of cow's milk or eight grams of milk protein powder
  • Pregnancy
  • A history of soy allergy
  • A history of food protein induced enterocolitis syndrome to milk
  • A history of anaphylaxis requiring hospitalization
  • A history of intubation related to asthma and/or a history of an intensive care unit admission for asthma management
  • A current diagnosis of severe persistent asthma [forced expiratory volume in 1 second (FEV1) < 60% of predicted, as defined by National Heart, Lung, and Blood Institute (NHLBI) guidelines, despite current therapy
  • A current diagnosis of severe atopic dermatitis
  • A serious chronic medical condition, including neurologic, hepatic, renal, endocrine, cardiovascular, gastrointestinal, pulmonary, or metabolic disease
  • Use of oral or injection steroids within one month of protocol initial visit
  • An acute illness within one week prior to the first dose of oral immunotherapy
  • Use of antihistamines within seven days prior to double blind placebo controlled food challenge (DBPCFC)
  • Use of chronic immunomodulatory therapy
  • Participation in another experimental therapy study
  • Participation in a study for the treatment of food allergy in the past 12 months
  • Inability to discontinue antihistamines for skin testing and food challenges

Treatment and study plan

Milk Oral Immunotherapy

Dietary Supplement

Subjects will participate in a desensitization protocol over the course of 13 weeks to reach a goal maintenance dose of 8 ounces of cow's milk. Once reaching maintenance, subjects will continue on this dose for 12 additional weeks.

Milk Protein Powder

Drug

Milk protein powder will be administered in incremental doses during the desensitization protocol.

Food Challenge

Other

Primary outcomes

  1. Number of Subjects Who Completed Desensitization Protocol

    Time frame: 1 year

    Subjects who withdrew prior to completing the desensitization protocol and those who experienced anaphylaxis during the desensitization protocol (i.e., were unable to complete the protocol) were considered to be "treatment failures". Subjects who completed the desensitization protocol were considered to be "treatment successes".

Sponsors and collaborators

Lead sponsor

Children's Hospital of Philadelphia

Other

Registry information

Official study title

A Study of the Efficacy of Milk Oral Immunotherapy in Children

Important dates

Study start
2010
Primary completion
2013
Study completion
2013
First posted
Jul 14, 2010
Registry last updated
May 13, 2015

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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