Growth And Safety Outcomes In Infants With Cow´s Milk Protein Allergy (CMPA) Fed A Novel Extensively Hydrolyzed Formula (eHF)

Starting soon · Not applicable

Conditions studied: Cow Milk Protein Allergy

In brief

Growth and safety Outcomes in infants with CMPA fed a novel extensively hydrolyzed formula.

Key facts

Study ID

NCT07711938

Run by

Société des Produits Nestlé (SPN)

People needed

410

Starts

2026-07-01

Expected to finish

2029-05-30

Last updated by the study team

2026-07-17

Who can join

Age: 0 and older, up to 0. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Full-term infant(gestational age ≥37 weeks and ≤42 weeks).
• Birth weight ≥2500 g and ≤4500 g.
• Parent(s)/LAR deemed able to provide written informed consent for participation of their infant in the study (in the opinion of the investigator).
• Participant aged ≥29 days (>4 weeks) and <5 months (≤22 weeks) at time of enrollment.
• Not breastfed at time of Screening Visit.
• History of an immediate-type (IgE-mediated) allergic reaction to a cow's milk-containing food or at least 2 persistent severe symptoms suggestive of delayed-onset (non-IgE-mediated) CMPA.

You may not qualify if…

• Prior use of eHF, HRF or AAF for more than 2 weeks before randomization.
• Congenital illness or malformation that may affect growth, or significant pre-natal and/or serious post-natal disease other than CMPA before randomization (per investigator's medical decision).
• Demonstrated chronic malabsorption not due to CMPA.
• History of severe anaphylaxis to CMP.
• Infants whose parent(s)/LAR cannot be expected to comply with study procedures.
• Currently participating or having participated in another clinical study since birth.
• Infants with a history of confirmed food protein induced enterocolitis syndrome due to other foods than CMP or Heiner syndrome.
• Infants with history of oral immunotherapy for CMPA.
• Diagnosed eosinophilic esophagitis.
• Received systemic oral or injected corticosteroids for more than 3 days (72 hours) within 2 weeks prior to the Screening Visit (topical corticosteroids allowed).
• Received systemic antibiotics within 1 week prior to Screening Visit (topical antibiotics, e.g., mupirocin allowed).
• Infants who are currently receiving treatment with immunomodulators (immunoglobulins, allergen extracts, or similar) or immuno-suppressants (azathioprine, cyclosporine or similar) within 2 weeks of Screening Visit (topical cyclosporine, tacrolimus, pimecrolimus or similar topical eczema treatments allowed), as well as infants with immune disorders which can compromise the immune function.
• Infants with a past or current disease or disorder which, in the opinion of the investigator or the sponsor either places the participant at risk because of participating in the study or may influence the results of the study, or the participant's ability to participate in the study (e.g., cardiovascular, pulmonary, gastrointestinal, hepatic, renal, neurological, musculoskeletal, endocrine or metabolic disorders, malignancy, major physical impairment, immunodeficiency, infectious disease or abnormal laboratory results as per the investigator's judgment).
• Parent(s)/LAR being in any relationship or dependency with the sponsor, and/or the investigator, and/or study staff.
• Underage parents (under 18 years old).

Full record on ClinicalTrials.gov

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