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Product Availability Due to Recall
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This is a multi-center, randomized, double-blind, placebo-controlled food challenge to be conducted in infants or children with confirmed IgE-mediated cow's milk allergy (CMA), followed by a 7-day open feeding of the experimental formula.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Experimental Extensively Hydrolyzed Formula | Experimental | Administered during food challenge and at home feeding period |
|
| Placebo Extensively Hydrolyzed Formula | Placebo Comparator | Administered during food challenge |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| Experimental Extensively Hydrolyzed Formula | Other | experimental powder formula |
|
| Measure | Description | Time Frame |
|---|---|---|
| Food Challenge Positive Reactions | Percent of positive food challenge reactions to the experimental formula | Food Challenge Day 1 to Food Challenge Day 2 |
| Measure | Description | Time Frame |
|---|---|---|
| Experimental Formula Intake | Parent completed diaries of formula intake | Home Feeding Day 1 to Day 7 |
| Food Intake | Parent completed diaries |
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Inclusion Criteria:
Participant has a physician diagnosis of IgE-mediated Cow's Milk Allergy (CMA) based on a clinical history of a reaction resulting in characteristic immediate hypersensitivity symptoms within 2 hours of oral exposure or immediate hypersensitivity symptoms according to physician's observation
Participant is willing to undergo confirmatory testing or must have had at least one of the following within 6 months of enrollment:
Participant agrees to stop oral steroid use within 14 days and antihistamine use within 7 days of confirmation of diagnosis and food challenges.
Participant had followed a strict cow's milk protein-free diet prior to enrollment.
Parent(s) confirm their intention not to administer any products containing cow's milk protein during the study.
Participant's parent(s) has voluntarily signed and dated an Informed Consent Form (ICF), approved by an Independent Ethics Committee/Institutional Review Board (IEC/IRB) and provided Health Insurance Portability and Accountability Act (HIPAA) (or other applicable privacy regulation) authorization prior to any participation in the study.
Exclusion Criteria:
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| Name | Affiliation | Role |
|---|---|---|
| Carlett Ramirez | Abbott Nutrition | Study Chair |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Children's Hospital Colorado | Aurora | Colorado | 80045 | United States | ||
| Children's Healthcare of Atlanta |
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| ID | Term |
|---|---|
| D016269 | Milk Hypersensitivity |
| ID | Term |
|---|---|
| D005512 | Food Hypersensitivity |
| D006969 | Hypersensitivity, Immediate |
| D006967 | Hypersensitivity |
| D007154 | Immune System Diseases |
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| Placebo Extensively Hydrolyzed Formula | Other | placebo powder formula |
|
| Home Feeding Day 1 to Day 7 |
| Gastrointestinal Symptoms | Parent completed diaries | Home Feeding Day 1 to Day 7 |
| Medication Use | Parent completed diaries | Home Feeding Day 1 to Day 7 |
| Food Challenge Positive Reactions | Percent of positive food challenge reactions to the experimental formula | Home Feeding Day 1 to Day 7 |
| Atlanta |
| Georgia |
| 30329 |
| United States |
| UNC-Chapel Hill | Chapel Hill | North Carolina | 27599 | United States |
| The Children's Hospital of Philadelphia | Philadelphia | Pennsylvania | 19104 | United States |