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COMPLETEDNANCT01998074

Evaluation of the Efficacy of a New Formula in Infants With Cow's Milk Protein Allergy

The aim of the study is to show the efficacy, tolerance and nutritional adequacy of a newly developed hydrolyzed rice formula in infants with a proven cow's milk protein allergy.

Lead sponsor: United Pharmaceuticals•1 locations•View source on ClinicalTrials.gov

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Sponsors

Lead Sponsor

United Pharmaceuticals

Age

0 - 0 years

Sex

ALL

Healthy Volunteers

No

Inclusion Criteria

•Infants between 2 weeks and 6 months old
•In whom cow's Milk Protein Allergy has been proved by a food challenge performed during the previous month

Exclusion Criteria

•Exclusively breast fed infants
•Preterm infants
•Infants already fed with an extensively hydrolyzed formula with no improvement of the symptoms.
•Infants fed an amino acid based formula
•Infants who had an anaphylactic reaction in the past

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A Registry for the Food Allergy Community

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Data from ClinicalTrials.govLast updated on ClinicalTrials.gov: November 28, 2013Terms

Trial snapshot

StatusCOMPLETED

PhaseNA

Enrollment—

Start date—

Last updatedNov 28, 2013

Condition

Milk Hypersensitivity Food Sensitivity Protein Allergy

Locations shown

Universitair Ziekenhuis

Brussels

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Data Source & Attribution

This clinical trial information is sourced from ClinicalTrials.gov, a service of the U.S. National Institutes of Health.

ClinicalTrials.gov last update: November 28, 2013Data synced to Clareo: June 28, 2026

Modifications: This data has been reformatted for display purposes. Eligibility criteria have been parsed into inclusion/exclusion sections. Location data has been geocoded to enable distance-based search. For the authoritative and most current information, please visit ClinicalTrials.gov.

Neither the United States Government nor Clareo Health make any warranties regarding the data. Check ClinicalTrials.gov frequently for updates.

View ClinicalTrials.gov Terms and Conditions