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Completed

NCT Number: NCT00732654

The Safety and Efficacy of Sublingual/Oral Immunotherapy for the Treatment of Milk Protein Allergy

The purpose of this study is to determine if small oral and sublingual doses of milk protein are safe and effective in decreasing sensitivity to cow's milk in allergic children.

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Key information

Age range

6 year–21 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 1 / Phase 2

Primary location

Johns Hopkins Hospital, Baltimore, Maryland, United States

Loading trial locations.

Who can participate

Healthy volunteers accepted: No

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

Inclusion criteria

  • Are age 6 to 21 years
  • Provide signed informed consent (by parent or legal guardian if the subject is a minor), and informed assent if applicable
  • Have a history of symptomatic reactivity to cow's milk (i.e. Eczema, urticaria, upper or lower respiratory symptoms, GI disturbances, other rash or oral symptoms)
  • Have a positive skin prick test (defined as wheal 3 mm ≥ negative control) and cow's milk- immunoglobulin E (IgE) > 0.35 kilo Immunoglobulin Units (kIU)/L
  • Have a positive OFC to cow's milk at a cumulative dose of less than 184 milligrams of cow's milk intact protein (2,400 mg total milk protein).
  • Are using appropriate birth control if subject is female and of child bearing age.
  • Have self-injectable epinephrine (ie. EpiPen® or EpiPen Jr.®) available at home

Exclusion criteria

  • Have a history of severe anaphylaxis defined as hypoxia (cyanosis or SpO2 ≤ 92% at any stage), hypotension, confusion, collapse, loss of consciousness; or incontinence
  • Have a history of intubation related to asthma
  • Tolerate more than 184 milligrams of intact cow's milk protein at initial OFC
  • Are pregnant or lactating
  • Have a viral Upper Respiratory Infection (URI) or gastroenteritis within 7 days of OFC (OFC needs to be rescheduled)
  • Have pulmonary function tests <80% of predicted (FEV1) or clinical history consistent with more than moderate persistent asthma
  • Are currently taking greater than medium dose inhaled corticosteroid (>400 mcg/day fluticasone or fluticasone equivalent if ≤ 12 years old or > 600 mcg/day if > 12 years old)
  • Are unable to discontinue antihistamines for 5 days for long acting and 3 days for short acting prior to skin testing or food challenges
  • Have used systemic corticosteroids within 4 weeks prior to baseline visit
  • Are receiving omalizumab, beta-blocker, Angiotensin Converting Enzyome (ACE) inhibitor or tricyclic antidepressant therapy
  • Have a chronic disease (other than asthma, atopic dermatitis or rhinitis) requiring therapy (e.g., heart disease, diabetes)
  • Have participated in any interventional study for treatment of a food allergy in the past 12 months
  • Have a severe reaction at initial DBPCFC, defined as either:

Life-threatening anaphylaxis, or Reaction requiring hospitalization

Treatment and study plan

Milk Protein Extract Immunotherapy goal of 4mg/day

Drug

Sublingual extract given daily in escalating doses with goal of 4 mg/day for approximately 20 weeks.

Milk Protein Extract Immunotherapy goal of 7mg/day

Drug

Sublingual extract daily in escalating doses to goal of 7mg/day for approximately 1 1/2 years.

Milk Powder Immunotherapy goal dose 2000 mg/day

Drug

Milk powder given orally in escalating doses with a goal dose of 2000mg/day given for approximately 1 1/2 years.

Milk Powder Immunotherapy goal dose 1000mg/day

Drug

Milk powder given orally in escalating doses with a goal of 1000mg/day for approximately 1 1/2 years.

Primary outcomes

  1. Change in CM-specific Immunogloblin E (IgE)

    Time frame: Change from baseline to after therapy (up to 18 months)

    Cow's milk specific IgE was measured at baseline and after therapy (kUa/L)

  2. Change in CM-specific Immunoglobulin G4 (IgG4)

    Time frame: Change from baseline to after therapy (up to 18 months)

    Cow's milk specific IgG4 was measured at baseline and after therapy (kUa/L)

  3. Change in End Point Skin Test

    Time frame: Change from baseline to after therapy (up to 18 months)

    Allergen provoked skin test (mm)

  4. Oral Food Challenge Threshold (OFC) Threshold

    Time frame: Change from baseline to after therapy (up to 18 months)

    mg CM protein

Sponsors and collaborators

Lead sponsor

Johns Hopkins University

Other

Collaborators

  • Duke University
  • Greer Laboratories

Registry information

Important dates

Study start
2008
Primary completion
2010
Study completion
2012
First posted
Aug 12, 2008
Registry last updated
May 15, 2017

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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