Trial Search Results

Dupilumab and Milk OIT for the Treatment of Cow's Milk Allergy

This is a phase 2, multicenter, randomized, double-blind, parallel group, 2 arm study in approximately 40 subjects aged 4 to 50 years, inclusive, who are allergic to cow's milk. The primary objective is to assess whether dupilumab as an adjunct to milk oral immunotherapy (OIT) compared to placebo improves the safety of milk OIT and rates of desensitization, defined as an increase in the proportion of subjects who pass a double-blind placebo-controlled food challenge (DBPCFC) to at least 2040 mg cumulative milk protein at week 18.

Stanford is currently accepting patients for this trial.

Lead Sponsor:

Andrew J Long, PharmD

Collaborator: Robert Levin Charitable Fund

Stanford Investigator(s):

Intervention(s):

  • Drug: Dupilumab
  • Other: Placebo

Phase:

Phase 2

Eligibility


Inclusion Criteria:

   - Age 4 to 50 years (inclusive)

   - Clinical history of allergy to cow's milk or milk-containing foods

   - Serum IgE to milk of >4 kUA/L within the last 12 months and/or a SPT to milk ≥6 mm
   compared to a negative control

   - Experience clinical reaction at or before 444 mg cumulative protein dose of cow's milk
   protein on Screening DBPCFC

   - No clinical reaction observed during the placebo (oat) Screening DBPCFC

   - Subjects with other known food allergies must agree to eliminate these other food
   items from their diet so as not to confound the safety and efficacy data from the
   study

   - Use of effective birth control by female participants of childbearing potential

Exclusion Criteria:

   - Any previous exposure to dupilumab

   - Known hypersensitivity to dupilumab or any of its excipients

   - Known hypersensitivity to epinephrine or any of its excipients

   - Allergy to oat (placebo in DBPCFC)

   - History of severe anaphylaxis to cow's milk, defined as neurological compromise or
   requiring intubation

   - Recent history of frequent severe, life-threatening episodes of anaphylaxis or
   anaphylactic shock as defined as 3 or more episodes of anaphylaxis within the past
   year

   - Inability to tolerate biological (antibody) therapies

   - Body weight ≤5 kg at the time of screening

   - History of eosinophilic esophagitis (EoE), other eosinophilic gastrointestinal
   disease, chronic, recurrent, or severe gastroesophageal reflux disease (GERD),
   symptoms of dysphagia (e.g., difficulty swallowing, food "getting stuck"), or
   recurrent gastrointestinal symptoms of undiagnosed etiology

   - History of cardiovascular disease, including uncontrolled or inadequately controlled
   hypertension

   - History of a mast cell disorder

   - Established diagnosis of a primary immunodeficiency disorder

   - Severe asthma or mild or moderate asthma if uncontrolled or difficult to control

   - Current participation or within the last 4 months in any other interventional study

   - Use of medication such as beta-blockers (oral), angiotensin-converting enzyme (ACE)
   inhibitors, angiotensin-receptor blockers (ARB) or calcium channel blockers

   - Pregnant or breastfeeding women

Ages Eligible for Study

4 Years - 50 Years

Genders Eligible for Study

All

Now accepting new patients

Contact Information

Stanford University
School of Medicine
300 Pasteur Drive
Stanford, CA 94305
Andrew Long, PharmD
650-724-0293
Recruiting